Variant report

Variant	esv3358936
Chromosome Location	chr14:81786719-81928269
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1901)
CpG islands
(count:1649)
Chromatin interactive
region (count:168)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1901 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:81868069-81868663	K562	blood:	n/a	n/a
2	ARID3A	chr14:81889809-81890253	K562	blood:	n/a	n/a
3	ARID3A	chr14:81898575-81898920	K562	blood:	n/a	n/a
4	ARID3A	chr14:81919538-81919980	K562	blood:	n/a	n/a
5	ARID3A	chr14:81919477-81919869	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:81874896-81875252	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:81887744-81887751	K562	blood:	n/a	n/a
8	ARID3A	chr14:81893733-81894537	K562	blood:	n/a	n/a
9	ARID3A	chr14:81866603-81866903	K562	blood:	n/a	n/a
10	ARID3A	chr14:81901267-81902062	K562	blood:	n/a	n/a
11	ARID3A	chr14:81825185-81825197	K562	blood:	n/a	n/a
12	ARID3A	chr14:81912793-81912950	HepG2	liver:	n/a	n/a
13	ARID3A	chr14:81900564-81900940	K562	blood:	n/a	n/a
14	ATF1	chr14:81898485-81898828	K562	blood:	n/a	n/a
15	ATF1	chr14:81900590-81901085	K562	blood:	n/a	n/a
16	ATF1	chr14:81893635-81894505	K562	blood:	n/a	n/a
17	ATF1	chr14:81889782-81890182	K562	blood:	n/a	n/a
18	ATF1	chr14:81882614-81883897	K562	blood:	n/a	n/a
19	ATF1	chr14:81815860-81816001	K562	blood:	n/a	n/a
20	ATF1	chr14:81868376-81868727	K562	blood:	n/a	n/a
21	ATF1	chr14:81866502-81866954	K562	blood:	n/a	n/a
22	ATF2	chr14:81867715-81868129	GM12878	blood:	n/a	n/a
23	ATF2	chr14:81867763-81868138	GM12878	blood:	n/a	n/a
24	ATF3	chr14:81868368-81868739	K562	blood:	n/a	n/a
25	ATF3	chr14:81898507-81898908	K562	blood:	n/a	n/a
26	ATF3	chr14:81866522-81866999	K562	blood:	n/a	chr14:81866678-81866688
27	ATF3	chr14:81894010-81894383	K562	blood:	n/a	n/a
28	BACH1	chr14:81893813-81894374	K562	blood:	n/a	n/a
29	BACH1	chr14:81868470-81868670	K562	blood:	n/a	n/a
30	BACH1	chr14:81901876-81903141	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr14:81866712-81867065	K562	blood:	n/a	n/a
32	BATF	chr14:81867798-81868064	GM12878	blood:	n/a	chr14:81868048-81868056
33	BCL11A	chr14:81867776-81868155	GM12878	blood:	n/a	chr14:81868139-81868146
34	BCLAF1	chr14:81894047-81894498	K562	blood:	n/a	n/a
35	BHLHE40	chr14:81893565-81894439	K562	blood:	n/a	n/a
36	BHLHE40	chr14:81867254-81867560	K562	blood:	n/a	n/a
37	BHLHE40	chr14:81909517-81909750	K562	blood:	n/a	n/a
38	BHLHE40	chr14:81902376-81902479	K562	blood:	n/a	n/a
39	BHLHE40	chr14:81889736-81890347	K562	blood:	n/a	n/a
40	BHLHE40	chr14:81868231-81868725	K562	blood:	n/a	n/a
41	BHLHE40	chr14:81866561-81867002	K562	blood:	n/a	n/a
42	BHLHE40	chr14:81926721-81926920	K562	blood:	n/a	n/a
43	BHLHE40	chr14:81882467-81883015	K562	blood:	n/a	n/a
44	BHLHE40	chr14:81900615-81901044	K562	blood:	n/a	n/a
45	BHLHE40	chr14:81906530-81906746	GM12878	blood:	n/a	n/a
46	BHLHE40	chr14:81901830-81902174	K562	blood:	n/a	n/a
47	BHLHE40	chr14:81926665-81926924	HepG2	liver:	n/a	n/a
48	BRCA1	chr14:81919633-81919968	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr14:81866499-81868180	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr14:81790234-81790800	Hela-S3	cervix:	n/a	n/a

(count:1649 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:81902346-81902396	AG09309	skin:	n/a
2	chr14:81902963-81903013	ProgFib	skin:	n/a
3	chr14:81902346-81902396	AG09309	skin:	n/a
4	chr14:81902963-81903013	ProgFib	skin:	n/a
5	chr14:81903146-81903196	ECC-1	luminal epithelium:	n/a
6	chr14:81832422-81832472	Caco-2	colon:	n/a
7	chr14:81864623-81864673	A549	lung:	n/a
8	chr14:81864899-81864949	HCM	heart:	n/a
9	chr14:81864643-81864693	HL-60	blood:	n/a
10	chr14:81879247-81879297	HNPCEpiC	eye:	n/a
11	chr14:81797427-81797477	HEK293	kidney:	embryo
12	chr14:81901907-81901957	PFSK-1	brain:	n/a
13	chr14:81879375-81879425	HCM	heart:	n/a
14	chr14:81901907-81901957	CMK	blood:	n/a
15	chr14:81902346-81902396	LNCaP	prostate:	n/a
16	chr14:81899486-81899536	HEEpiC	esophagus:	n/a
17	chr14:81902963-81903013	SKMC	muscle:	n/a
18	chr14:81902736-81902786	A549	lung:	n/a
19	chr14:81879375-81879425	Caco-2	colon:	n/a
20	chr14:81903146-81903196	HL-60	blood:	n/a
21	chr14:81832422-81832472	HL-60	blood:	n/a
22	chr14:81797427-81797477	HIPEpiC	eye:	n/a
23	chr14:81902346-81902396	GM12878	blood:	n/a
24	chr14:81902154-81902204	HRE	kidney:	n/a
25	chr14:81916652-81916702	H1-hESC	embryonic stem cell:	embryo
26	chr14:81865007-81865057	MCF-7	breast:	n/a
27	chr14:81852444-81852494	IMR90	lung:	fetal
28	chr14:81902346-81902396	GM12891	blood:	n/a
29	chr14:81894673-81894723	U87	brain:	n/a
30	chr14:81894673-81894723	A549	lung:	n/a
31	chr14:81902736-81902786	HCT-116	colon:	n/a
32	chr14:81902974-81903024	HCM	heart:	n/a
33	chr14:81893864-81893914	GM12891	blood:	n/a
34	chr14:81916652-81916702	SK-N-SH	brain:	n/a
35	chr14:81893829-81893879	BE2_C	brain:	n/a
36	chr14:81905381-81905431	GM12891	blood:	n/a
37	chr14:81901540-81901590	HCT-116	colon:	n/a
38	chr14:81864643-81864693	Hepatocyte	liver:	n/a
39	chr14:81899486-81899536	A549	lung:	n/a
40	chr14:81902154-81902204	HEEpiC	esophagus:	n/a
41	chr14:81865007-81865057	IMR90	lung:	fetal
42	chr14:81832422-81832472	A549	lung:	n/a
43	chr14:81916652-81916702	ECC-1	luminal epithelium:	n/a
44	chr14:81864623-81864673	HAEpiC	amniotic membrane:	n/a
45	chr14:81905381-81905431	SAEC	small airway:	n/a
46	chr14:81864643-81864693	AG04450	lung:	fetal
47	chr14:81902154-81902204	HL-60	blood:	n/a
48	chr14:81916652-81916702	HEK293	kidney:	embryo
49	chr14:81797427-81797477	CMK	blood:	n/a
50	chr14:81879247-81879297	HUVEC	blood vessel:	n/a

(count:168 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr11:61841676..61843276-chr14:81785709..81787593,4	MCF-7	breast:
2	chr14:81871493..81873378-chr14:81876007..81877708,2	K562	blood:
3	chr14:81686323..81687896-chr14:81840173..81843007,2	MCF-7	breast:
4	chr14:81791324..81793435-chr14:81918105..81920642,2	MCF-7	breast:
5	chr14:81881608..81884227-chr14:81901358..81903544,2	K562	blood:
6	chr14:81867720..81869556-chr14:81873808..81876587,2	MCF-7	breast:
7	chr14:81685776..81687445-chr14:81891086..81893956,2	K562	blood:
8	chr14:81787114..81788758-chr14:81816249..81818905,2	K562	blood:
9	chr14:81683389..81688783-chr14:81897521..81903580,11	MCF-7	breast:
10	chr14:81900712..81903820-chr14:81907032..81909631,3	K562	blood:
11	chr14:81829800..81831897-chr14:81837300..81840056,2	MCF-7	breast:
12	chr14:81807853..81809549-chr14:81809660..81812402,2	K562	blood:
13	chr14:81810357..81812474-chr14:81820150..81822566,2	K562	blood:
14	chr14:81901271..81902197-chr9:83452129..83452649,2	MCF-7	breast:
15	chr14:81783553..81785269-chr14:81899174..81901080,2	MCF-7	breast:
16	chr14:81788554..81792307-chr14:81796466..81799026,4	MCF-7	breast:
17	chr14:81849841..81851536-chr14:81894203..81896873,2	K562	blood:
18	chr14:81834534..81837450-chr14:81839716..81841468,3	K562	blood:
19	chr14:81685661..81688388-chr14:81920051..81922947,2	K562	blood:
20	chr14:81849841..81851536-chr14:81894203..81896873,2	K562	blood:
21	chr14:81867029..81868586-chr14:81887440..81889989,2	K562	blood:
22	chr14:81882721..81884801-chr14:81890503..81892167,2	K562	blood:
23	chr14:81768674..81769277-chr14:81919339..81919953,2	MCF-7	breast:
24	chr14:81837694..81839198-chr14:81840938..81842642,2	MCF-7	breast:
25	chr14:81855959..81858905-chr14:81901728..81904527,2	K562	blood:
26	chr14:81835420..81837863-chr14:81857937..81859970,2	MCF-7	breast:
27	chr14:81870339..81872408-chr14:81882068..81884278,2	K562	blood:
28	chr14:81732900..81735880-chr14:81918109..81921076,5	MCF-7	breast:
29	chr14:81685715..81687789-chr14:81806873..81809588,4	MCF-7	breast:
30	chr14:81684550..81687395-chr14:81881105..81883883,2	K562	blood:
31	chr14:81682072..81683582-chr14:81925884..81928192,2	MCF-7	breast:
32	chr14:81740539..81742238-chr14:81855597..81857728,2	MCF-7	breast:
33	chr14:81866745..81868446-chr14:81903093..81904882,2	K562	blood:
34	chr14:81870339..81872408-chr14:81882068..81884278,2	K562	blood:
35	chr14:81685490..81687621-chr14:81866238..81868620,4	MCF-7	breast:
36	chr14:81867994..81870092-chr14:81876125..81877918,2	K562	blood:
37	chr14:81686697..81688459-chr14:81858395..81860078,2	MCF-7	breast:
38	chr14:81685770..81687296-chr14:81799417..81802268,2	K562	blood:
39	chr14:81685691..81688551-chr14:81879364..81882605,3	K562	blood:
40	chr14:81684506..81688423-chr14:81892845..81897193,10	K562	blood:
41	chr14:81866040..81868691-chr14:81870203..81872674,2	K562	blood:
42	chr14:81852266..81853780-chr14:81865825..81868508,2	K562	blood:
43	chr14:81903553..81905384-chr14:81907954..81910407,2	MCF-7	breast:
44	chr14:81865587..81872038-chr14:81887440..81896764,13	K562	blood:
45	chr14:81686251..81689085-chr14:81904522..81908171,4	K562	blood:
46	chr14:81847233..81850100-chr14:81861547..81864501,2	MCF-7	breast:
47	chr14:81735897..81736529-chr14:81919200..81920174,5	K562	blood:
48	chr14:81684220..81688666-chr14:81897892..81904337,14	K562	blood:
49	chr14:81686224..81688353-chr14:81839920..81841889,2	K562	blood:
50	chr14:81865287..81867829-chr14:81917916..81919892,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SEL1L-11	chr14:81890821-81890830	NONHSAT038064
2	lnc-SEL1L-11	chr14:81881291-81881385	NONHSAT038064
3	lnc-STON2-1	chr14:81908331-81908540	ENSG00000258675
4	lnc-SEL1L-11	chr14:81893446-81893558	NONHSAT038064
5	lnc-SEL1L-11	chr14:81890962-81891681	NONHSAT038064
6	lnc-STON2-1	chr14:81916233-81916501	ENSG00000258675
7	lnc-STON2-1	chr14:81908629-81908786	ENSG00000258675
8	lnc-GTF2A1-4	chr14:81799305-81799705	NONHSAT038063

No data

Variant related genes	Relation type
ENSG00000258605	TF binding region
ENSG00000258675	TF binding region
STON2	TF binding region
ENSG00000242163	TF binding region
ENSG00000258605	CpG island
ENSG00000258675	CpG island
STON2	CpG island
ENSG00000242163	CpG island
ENSG00000100629	chromatin interactions
ENSG00000140022	chromatin interactions
ENSG00000242163	chromatin interactions
ENSG00000165417	chromatin interactions
ENSG00000258675	chromatin interactions
ENSG00000152256	chromatin interactions
ENSG00000225205	chromatin interactions

Extended variants
information (count: 5547 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:5547 , 50 per page) page: 1 2 3 4 5 6 7 ... 111

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542679134	chr14:81786722-81786723	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs374133442	chr14:81786737-81786738	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs555619828	chr14:81786761-81786762	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs201820136	chr14:81786772-81786773	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs181884507	chr14:81786777-81786778	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs201292236	chr14:81786783-81786784	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs372266438	chr14:81786785-81786786	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs375293885	chr14:81786786-81786787	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs572915990	chr14:81786801-81786802	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs74910359	chr14:81786809-81786810	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs537643998	chr14:81786827-81786828	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs371955644	chr14:81786863-81786864	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs555940442	chr14:81786865-81786866	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs577673496	chr14:81786902-81786903	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs545497665	chr14:81786919-81786920	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs554003387	chr14:81786996-81786997	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs572391903	chr14:81787093-81787094	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs80236237	chr14:81787102-81787103	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs532046121	chr14:81787145-81787146	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs576803005	chr14:81787150-81787151	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs529358186	chr14:81787241-81787242	Weak transcription Enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs12437268	chr14:81787255-81787256	Weak transcription Enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs532858511	chr14:81787291-81787292	Weak transcription Enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs114833902	chr14:81787381-81787382	Weak transcription Enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs566479543	chr14:81787393-81787394	Weak transcription Enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs527269692	chr14:81787400-81787401	Weak transcription Enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs548612136	chr14:81787416-81787417	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs567173358	chr14:81787433-81787434	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs377631236	chr14:81787476-81787477	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs3109610	chr14:81787481-81787482	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs58943901	chr14:81787482-81787483	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs571090255	chr14:81787564-81787565	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs538492937	chr14:81787577-81787578	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs530884667	chr14:81787582-81787583	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs554233444	chr14:81787646-81787647	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs549109727	chr14:81787677-81787678	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs536602498	chr14:81787691-81787692	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs566882924	chr14:81787715-81787716	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs397968781	chr14:81787733-81787734	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs376765777	chr14:81787734-81787735	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs555013699	chr14:81787781-81787782	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs576776459	chr14:81787859-81787860	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs544151491	chr14:81787966-81787967	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs187328345	chr14:81788021-81788022	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs567285478	chr14:81788051-81788052	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs577352249	chr14:81788116-81788117	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs541303319	chr14:81788146-81788147	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs560190304	chr14:81788205-81788206	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs532399481	chr14:81788215-81788216	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs57982987	chr14:81788235-81788236	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16608533	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Glioblastoma	21080181	CNVD
Gastric cancer	16891809	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD

Chromatin state (count:2961 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:81773600-81790600	Weak transcription	K562	blood
2	chr14:81778400-81810800	Weak transcription	Primary hematopoietic stem cells	blood
3	chr14:81778600-81789200	Weak transcription	Esophagus	oesophagus
4	chr14:81779600-81787000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr14:81779600-81788200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr14:81780600-81790400	Weak transcription	Fetal Muscle Trunk	muscle
7	chr14:81781000-81798400	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr14:81781200-81792400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr14:81782000-81787000	Weak transcription	Spleen	Spleen
10	chr14:81782200-81790200	Weak transcription	Placenta	Placenta
11	chr14:81782200-81790600	Weak transcription	Psoas Muscle	Psoas
12	chr14:81782400-81788400	Weak transcription	Brain Cingulate Gyrus	brain
13	chr14:81782400-81789000	Weak transcription	Brain Hippocampus Middle	brain
14	chr14:81782600-81790200	Weak transcription	Fetal Muscle Leg	muscle
15	chr14:81782800-81788800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr14:81783000-81787400	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr14:81783000-81788000	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr14:81783000-81788000	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr14:81783000-81788800	Weak transcription	Fetal Kidney	kidney
20	chr14:81783000-81789000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr14:81783000-81789000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr14:81783600-81787000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr14:81783600-81788000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr14:81783600-81788600	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr14:81784000-81787200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
26	chr14:81784000-81787400	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr14:81784200-81789200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr14:81784800-81786800	Enhancers	HepG2	liver
29	chr14:81785000-81787000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr14:81785200-81787600	Enhancers	Fetal Intestine Small	intestine
31	chr14:81785400-81787000	Enhancers	Fetal Intestine Large	intestine
32	chr14:81786200-81787200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr14:81786200-81787200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr14:81786400-81788600	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr14:81786600-81786800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr14:81786600-81786800	Weak transcription	HMEC	breast
37	chr14:81786600-81787000	Enhancers	NHEK	skin
38	chr14:81786600-81787200	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr14:81786600-81788000	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr14:81786600-81788600	Weak transcription	Stomach Mucosa	stomach
41	chr14:81786600-81789000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr14:81786600-81789400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr14:81786800-81787200	Weak transcription	HepG2	liver
44	chr14:81786800-81787600	Enhancers	HMEC	breast
45	chr14:81786800-81788600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr14:81787000-81787400	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr14:81787000-81787400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
48	chr14:81787000-81787400	Enhancers	Spleen	Spleen
49	chr14:81787000-81787600	Flanking Active TSS	NHEK	skin
50	chr14:81787000-81788200	Weak transcription	Fetal Intestine Large	intestine

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