Variant report

Variant	esv3518899
Chromosome Location	chr14:21805983-22077584
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5719)
CpG islands
(count:5683)
Chromatin interactive
region (count:389)
LncRNA
region (count:28)
Mature miRNA
region (count: 0)
miRNA target
sites (count:6)

(count:5719 , 50 per page) page: 1 2 3 4 5 6 7 ... 115

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:21944489-21944740	K562	blood:	n/a	n/a
2	ARID3A	chr14:21905341-21905986	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:21923992-21924994	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:21945015-21945422	K562	blood:	n/a	n/a
5	ARID3A	chr14:22025640-22026131	K562	blood:	n/a	n/a
6	ARID3A	chr14:21994992-21995458	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:21966671-21967139	HepG2	liver:	n/a	n/a
8	ARID3A	chr14:21905416-21905636	K562	blood:	n/a	n/a
9	ARID3A	chr14:21923518-21923683	HepG2	liver:	n/a	n/a
10	ARID3A	chr14:21943952-21944111	K562	blood:	n/a	n/a
11	ARID3A	chr14:21996539-21997519	K562	blood:	n/a	n/a
12	ARID3A	chr14:21994448-21994458	K562	blood:	n/a	n/a
13	ARID3A	chr14:21993728-21993871	K562	blood:	n/a	n/a
14	ARID3A	chr14:21979291-21979782	HepG2	liver:	n/a	chr14:21979443-21979458
15	ARID3A	chr14:21944173-21945505	HepG2	liver:	n/a	n/a
16	ARID3A	chr14:21966738-21967030	K562	blood:	n/a	n/a
17	ARID3A	chr14:22025455-22026095	HepG2	liver:	n/a	n/a
18	ARID3A	chr14:21851928-21852749	HepG2	liver:	n/a	n/a
19	ARID3A	chr14:21996905-21997545	HepG2	liver:	n/a	n/a
20	ARID3A	chr14:21945763-21945767	HepG2	liver:	n/a	n/a
21	ARID3A	chr14:21994508-21994645	HepG2	liver:	n/a	n/a
22	ATF1	chr14:21945060-21945516	K562	blood:	n/a	n/a
23	ATF1	chr14:21924142-21924679	K562	blood:	n/a	n/a
24	ATF1	chr14:21979341-21979788	K562	blood:	n/a	n/a
25	ATF1	chr14:21905327-21905918	K562	blood:	n/a	n/a
26	ATF1	chr14:21909009-21909364	K562	blood:	n/a	n/a
27	ATF1	chr14:21851977-21852775	K562	blood:	n/a	n/a
28	ATF1	chr14:21997147-21997541	K562	blood:	n/a	n/a
29	ATF2	chr14:21995072-21995731	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF2	chr14:21851976-21852780	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF2	chr14:21851922-21852515	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF2	chr14:21979271-21979788	H1-hESC	embryonic stem cell:	n/a	n/a
33	ATF2	chr14:21979113-21979851	GM12878	blood:	n/a	n/a
34	ATF2	chr14:21924321-21925038	GM12878	blood:	n/a	n/a
35	ATF2	chr14:21944987-21945661	GM12878	blood:	n/a	n/a
36	ATF2	chr14:21882139-21882796	GM12878	blood:	n/a	n/a
37	ATF2	chr14:21945128-21945466	H1-hESC	embryonic stem cell:	n/a	n/a
38	ATF2	chr14:22004310-22004890	H1-hESC	embryonic stem cell:	n/a	n/a
39	ATF2	chr14:22025452-22026111	H1-hESC	embryonic stem cell:	n/a	n/a
40	ATF2	chr14:22025504-22026106	H1-hESC	embryonic stem cell:	n/a	n/a
41	ATF2	chr14:21924544-21924861	H1-hESC	embryonic stem cell:	n/a	n/a
42	ATF2	chr14:21973180-21973706	GM12878	blood:	n/a	n/a
43	ATF2	chr14:22002656-22003267	H1-hESC	embryonic stem cell:	n/a	n/a
44	ATF2	chr14:21851272-21853025	GM12878	blood:	n/a	n/a
45	ATF2	chr14:21853276-21853708	GM12878	blood:	n/a	n/a
46	ATF2	chr14:21905255-21905664	H1-hESC	embryonic stem cell:	n/a	n/a
47	ATF2	chr14:21979242-21979799	H1-hESC	embryonic stem cell:	n/a	n/a
48	ATF2	chr14:21905204-21905788	GM12878	blood:	n/a	n/a
49	ATF2	chr14:21851939-21852728	GM12878	blood:	n/a	n/a
50	ATF2	chr14:21905255-21905759	H1-hESC	embryonic stem cell:	n/a	n/a

(count:5683 , 50 per page) page: 1 2 3 4 5 6 7 ... 114

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:21979401-21979451	HRCEpiC	kidney:	n/a
2	chr14:21820190-21820240	HUVEC	blood vessel:	n/a
3	chr14:21979401-21979451	CMK	blood:	n/a
4	chr14:21860787-21860837	GM12891	blood:	n/a
5	chr14:21860384-21860434	AG04450	lung:	fetal
6	chr14:21989279-21989329	SK-N-SH_RA	brain:	n/a
7	chr14:21852452-21852502	U87	brain:	n/a
8	chr14:21905982-21906032	AG04450	lung:	fetal
9	chr14:21979151-21979201	U87	brain:	n/a
10	chr14:21942464-21942514	RPTEC	kidney:	n/a
11	chr14:21979401-21979451	HRCEpiC	kidney:	n/a
12	chr14:21820190-21820240	HUVEC	blood vessel:	n/a
13	chr14:21979401-21979451	CMK	blood:	n/a
14	chr14:21860787-21860837	GM12891	blood:	n/a
15	chr14:21860384-21860434	AG04450	lung:	fetal
16	chr14:21989279-21989329	SK-N-SH_RA	brain:	n/a
17	chr14:21852452-21852502	U87	brain:	n/a
18	chr14:21905982-21906032	AG04450	lung:	fetal
19	chr14:21979151-21979201	U87	brain:	n/a
20	chr14:21942464-21942514	RPTEC	kidney:	n/a
21	chr14:22039806-22039856	RPTEC	kidney:	n/a
22	chr14:21852452-21852502	MCF10A-Er-Src	breast:	n/a
23	chr14:21900820-21900870	GM12878	blood:	n/a
24	chr14:21979673-21979723	AG09309	skin:	n/a
25	chr14:21905552-21905602	SKMC	muscle:	n/a
26	chr14:21852452-21852502	NT2-D1	testis:	n/a
27	chr14:21899991-21900041	GM12892	blood:	n/a
28	chr14:21945223-21945273	HMEC	breast:	n/a
29	chr14:21924393-21924443	NH-A	brain:	n/a
30	chr14:22038276-22038326	PANC-1	pancreas:	n/a
31	chr14:21853470-21853520	SK-N-SH_RA	brain:	n/a
32	chr14:22005948-22005998	HMEC	breast:	n/a
33	chr14:21927732-21927782	BE2_C	brain:	n/a
34	chr14:21866828-21866878	ECC-1	luminal epithelium:	n/a
35	chr14:21923087-21923137	HCM	heart:	n/a
36	chr14:21944873-21944923	HRCEpiC	kidney:	n/a
37	chr14:22039001-22039051	SK-N-SH_RA	brain:	n/a
38	chr14:21852549-21852599	BE2_C	brain:	n/a
39	chr14:21852452-21852502	HepG2	liver:	n/a
40	chr14:21853037-21853087	Hepatocyte	liver:	n/a
41	chr14:21905982-21906032	NB4	blood:	n/a
42	chr14:21945858-21945908	AG10803	skin:	n/a
43	chr14:21945175-21945225	GM12892	blood:	n/a
44	chr14:21975215-21975265	Caco-2	colon:	n/a
45	chr14:21924453-21924503	MCF10A-Er-Src	breast:	n/a
46	chr14:21852549-21852599	HPAEpiC	pulmonary alveolar:	n/a
47	chr14:21945223-21945273	HEEpiC	esophagus:	n/a
48	chr14:21820190-21820240	HCPEpiC	choroid plexus:	n/a
49	chr14:21905982-21906032	SK-N-MC	brain:	n/a
50	chr14:21860787-21860837	AG04449	skin:	fetal

(count:389 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Distal block	Cell Line	Cell type
1	chr14:21958167..21960481-chr14:21978207..21981018,2	MCF-7	breast:
2	chr14:21849377..21851145-chr14:21883237..21885715,2	K562	blood:
3	chr14:21994313..21997076-chr14:21999911..22001555,2	K562	blood:
4	chr14:21924214..21926252-chr14:21977009..21978995,2	K562	blood:
5	chr14:21970942..21973868-chr14:21992084..21994345,2	MCF-7	breast:
6	chr14:21969916..21972018-chr14:21978032..21980758,3	K562	blood:
7	chr14:21851767..21854140-chr14:21865544..21868214,2	K562	blood:
8	chr14:21826685..21830203-chr14:21830664..21832623,3	K562	blood:
9	chr14:21811333..21813148-chr14:21813647..21817148,3	K562	blood:
10	chr14:21820835..21822896-chr14:21824252..21825918,2	K562	blood:
11	chr14:21932234..21934143-chr14:21934754..21937508,2	MCF-7	breast:
12	chr14:21926286..21927863-chr14:21941529..21943943,2	K562	blood:
13	chr14:21906849..21909537-chr14:21910523..21912102,2	MCF-7	breast:
14	chr14:21904676..21909671-chr14:21916010..21919638,5	MCF-7	breast:
15	chr14:21802656..21804899-chr14:21816429..21817981,2	K562	blood:
16	chr14:21814821..21817594-chr14:21819098..21821242,4	K562	blood:
17	chr14:21945641..21947338-chr14:21977414..21979762,2	K562	blood:
18	chr14:21826685..21830203-chr14:21830664..21832623,3	K562	blood:
19	chr14:21972318..21975113-chr14:21978008..21980143,3	K562	blood:
20	chr14:21820226..21822237-chr14:21826339..21828894,2	K562	blood:
21	chr14:21826480..21828458-chr14:21851122..21853921,3	MCF-7	breast:
22	chr14:21920487..21922839-chr14:22025692..22028469,2	K562	blood:
23	chr14:21885310..21887748-chr14:21890138..21892937,2	K562	blood:
24	chr14:21927790..21931604-chr14:21933413..21935482,4	K562	blood:
25	chr14:21903666..21907303-chr14:21944223..21946943,4	K562	blood:
26	chr14:21978852..21980504-chr14:22026086..22028034,2	MCF-7	breast:
27	chr14:21904638..21906944-chr14:21907761..21909355,3	MCF-7	breast:
28	chr14:21728172..21729704-chr14:21921485..21922985,2	K562	blood:
29	chr14:21883102..21885831-chr14:21901937..21903563,2	K562	blood:
30	chr14:21943958..21946610-chr14:21966325..21968366,2	MCF-7	breast:
31	chr14:21904171..21908174-chr14:21922677..21925847,6	K562	blood:
32	chr14:21991104..21993583-chr14:21997557..21999607,2	MCF-7	breast:
33	chr14:21922783..21924510-chr14:22020238..22022205,2	K562	blood:
34	chr14:21932869..21935832-chr14:21936427..21939516,4	K562	blood:
35	chr14:21737007..21739696-chr14:21870070..21871764,2	MCF-7	breast:
36	chr14:21812370..21815159-chr14:21817089..21819526,2	MCF-7	breast:
37	chr14:21840421..21844645-chr14:21849472..21852747,5	K562	blood:
38	chr14:21729320..21731037-chr14:21850307..21852347,2	K562	blood:
39	chr14:21993529..21997076-chr14:21999911..22003110,4	K562	blood:
40	chr14:21935572..21937160-chr14:21965846..21967879,2	MCF-7	breast:
41	chr14:21903199..21908176-chr14:21922150..21927422,17	MCF-7	breast:
42	chr14:21969916..21972018-chr14:21978032..21980758,3	K562	blood:
43	chr14:21943174..21947446-chr14:21976603..21980796,8	K562	blood:
44	chr14:21908719..21910349-chr14:21917450..21919306,2	K562	blood:
45	chr14:21922495..21926195-chr14:21936351..21938953,4	MCF-7	breast:
46	chr14:21941797..21947093-chr14:21954513..21961521,11	MCF-7	breast:
47	chr14:21943174..21944974-chr14:21977836..21979361,2	K562	blood:
48	chr14:21839767..21842102-chr14:21844201..21846958,2	K562	blood:
49	chr14:21927480..21929708-chr14:21977698..21979335,2	K562	blood:
50	chr14:21924729..21926347-chr14:21926408..21928201,2	K562	blood:

(count:28 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RPGRIP1-1	chr14:21852451-21853079	ENSG00000260830.1
2	lnc-SALL2-1	chr14:21978710-21979055	NONHSAT035695
3	lnc-TOX4-2	chr14:21887779-21888119	NONHSAT035685
4	lnc-RAB2B-1	chr14:21897669-21897965	NONHSAT035686
5	lnc-SALL2-1	chr14:21976035-21976377	NONHSAT035694
6	lnc-TOX4-1	chr14:21990540-21990794	ENSG00000257096.1
7	lnc-CHD8-1	chr14:21911321-21911699	NONHSAT035689
8	lnc-CHD8-1	chr14:21921422-21921753	NONHSAT035689
9	lnc-CHD8-1	chr14:21905353-21905457	NONHSAT035688
10	lnc-CHD8-1	chr14:21920031-21920326	NONHSAT035689
11	lnc-CHD8-1	chr14:21915532-21916694	NONHSAT035689
12	lnc-OR10G3-1	chr14:22053414-22054404	NONHSAT035698
13	lnc-SALL2-1	chr14:21978797-21979122	NONHSAT035696
14	lnc-CHD8-1	chr14:22020070-22020187	ucscGeneNc_uc001wds_1
15	lnc-RPGRIP1-3	chr14:21867084-21867441	NONHSAT035684
16	lnc-CHD8-1	chr14:21924191-21924285	NONHSAT035687
17	lnc-CHD8-1	chr14:22021682-22021788	ucscGeneNc_uc001wds_1
18	lnc-TOX4-1	chr14:21989234-21989450	ENSG00000257096.1
19	lnc-CHD8-1	chr14:21924191-21924249	NONHSAT035689
20	lnc-CHD8-1	chr14:21920436-21920463	NONHSAT035689
21	lnc-SALL2-1	chr14:21979266-21979482	NONHSAT035694
22	lnc-SALL2-1	chr14:21979266-21979482	NONHSAT035695
23	lnc-CHD8-1	chr14:21899897-21900017	NONHSAT035688
24	lnc-CHD8-1	chr14:21918923-21920648	ucscGeneNc_uc001wds_1
25	lnc-CHD8-1	chr14:21899892-21900017	NONHSAT035687
26	lnc-SALL2-1	chr14:21979266-21979484	NONHSAT035696
27	lnc-CHD8-1	chr14:21923108-21923302	NONHSAT035687
28	lnc-CHD8-1	chr14:21905060-21905124	NONHSAT035688

No data

(count:6 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	SUPT16H	hsa-miR-16-5p	chr14:21819925-21819945
2	SUPT16H	hsa-miR-16-5p	chr14:21851303-21851322
3	RAB2B	hsa-miR-421	chr14:21927219-21927240
4	SUPT16H	hsa-miR-25-3p	chr14:21820642-21820664
5	SUPT16H	hsa-miR-615-3p	chr14:21820188-21820211
6	SUPT16H	hsa-miR-16-5p	chr14:21819931-21819925

Variant related genes	Relation type
TOX4	TF binding region
ENSG00000241035	TF binding region
EIF4EBP1P1	TF binding region
ENSG00000260830	TF binding region
RAB2B	TF binding region
SUPT16H	TF binding region
ENSG00000256081	TF binding region
OR10G1P	TF binding region
OR10G3	TF binding region
SALL2	TF binding region
SNORD8	TF binding region
ENSG00000257096	TF binding region
RN7SL650P	TF binding region
SNORD9	TF binding region
METTL3	TF binding region
RBBP4P5	TF binding region
CHD8	TF binding region
TOX4	CpG island
ENSG00000241035	CpG island
EIF4EBP1P1	CpG island
ENSG00000260830	CpG island
RAB2B	CpG island
SUPT16H	CpG island
ENSG00000256081	CpG island
OR10G1P	CpG island
OR10G3	CpG island
SALL2	CpG island
SNORD8	CpG island
ENSG00000257096	CpG island
RN7SL650P	CpG island
SNORD9	CpG island
METTL3	CpG island
RBBP4P5	CpG island
CHD8	CpG island
ENSG00000100883	chromatin interactions
ENSG00000197153	chromatin interactions
ENSG00000256081	chromatin interactions
ENSG00000257096	chromatin interactions
ENSG00000199436	chromatin interactions
ENSG00000255569	chromatin interactions
ENSG00000260830	chromatin interactions
ENSG00000204569	chromatin interactions
ENSG00000165821	chromatin interactions
ENSG00000165795	chromatin interactions
ENSG00000092203	chromatin interactions
ENSG00000249944	chromatin interactions
ENSG00000092200	chromatin interactions
ENSG00000134905	chromatin interactions
ENSG00000256737	chromatin interactions
ENSG00000165476	chromatin interactions
ENSG00000184270	chromatin interactions
ENSG00000241035	chromatin interactions
ENSG00000129472	chromatin interactions
ENSG00000153487	chromatin interactions
ENSG00000254635	chromatin interactions
ENSG00000256385	chromatin interactions
ENSG00000112701	chromatin interactions
ENSG00000196262	chromatin interactions
ENSG00000258704	chromatin interactions
ENSG00000165819	chromatin interactions
ENSG00000263621	chromatin interactions
ENSG00000200785	chromatin interactions
ENSG00000165801	chromatin interactions
ENSG00000206630	chromatin interactions
ENSG00000092201	chromatin interactions
ENSG00000100888	chromatin interactions
ENSG00000184260	chromatin interactions
ENSG00000166295	chromatin interactions
ENSG00000196331	chromatin interactions
ENSG00000095787	chromatin interactions
ENSG00000092199	chromatin interactions
ENSG00000127540	chromatin interactions
ENSG00000260260	chromatin interactions
ENSG00000178096	chromatin interactions
ENSG00000138303	chromatin interactions
ENSG00000233224	chromatin interactions
ENSG00000236352	chromatin interactions
ENSG00000141232	chromatin interactions
ENSG00000204054	chromatin interactions
ENSG00000267059	chromatin interactions
ENSG00000172809	chromatin interactions

Extended variants
information (count: 10097 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:10097 , 50 per page) page: 1 2 3 4 5 6 7 ... 202

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577844204	chr14:21805993-21805994	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs61977492	chr14:21806027-21806028	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs564048956	chr14:21806098-21806099	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs529520143	chr14:21806124-21806125	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs59933465	chr14:21806136-21806137	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs557230141	chr14:21806138-21806139	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs561493351	chr14:21806142-21806143	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs543831746	chr14:21806149-21806150	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs527262170	chr14:21806167-21806168	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs547543297	chr14:21806189-21806190	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs570561234	chr14:21806194-21806195	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs144504044	chr14:21806200-21806201	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs549671689	chr14:21806224-21806225	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs569934073	chr14:21806225-21806226	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs60373936	chr14:21806265-21806266	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs56764444	chr14:21806266-21806267	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs565972637	chr14:21806276-21806277	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs374744983	chr14:21806289-21806290	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs534675652	chr14:21806311-21806312	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs67347649	chr14:21806322-21806323	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs577704950	chr14:21806342-21806343	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs182298786	chr14:21806345-21806346	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs187706277	chr14:21806355-21806356	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs12586276	chr14:21806358-21806359	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs192571151	chr14:21806391-21806392	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs61977494	chr14:21806399-21806400	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs112980489	chr14:21806422-21806423	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs61977495	chr14:21806430-21806431	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs564181393	chr14:21806463-21806464	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs533013056	chr14:21806486-21806487	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs113792235	chr14:21806495-21806496	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs569715463	chr14:21806496-21806497	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs11848323	chr14:21806500-21806501	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs184241665	chr14:21806501-21806502	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs188410679	chr14:21806517-21806518	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs534737313	chr14:21806577-21806578	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs193194813	chr14:21806591-21806592	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs116293040	chr14:21806633-21806634	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs537117429	chr14:21806645-21806646	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs34381211	chr14:21806666-21806667	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs34436593	chr14:21806668-21806669	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs367545179	chr14:21806670-21806671	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs71419129	chr14:21806686-21806687	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs574179712	chr14:21806723-21806724	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs61977496	chr14:21806785-21806786	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs553432936	chr14:21806806-21806807	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs145472034	chr14:21806818-21806819	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs573540233	chr14:21806854-21806855	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs541032904	chr14:21806857-21806858	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs184743419	chr14:21806900-21806901	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Cancer	20164920	CNVD
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
Cone-rod dystrophy	18421352	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	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
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	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
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	21482944	CNVD
Mental retardation	19951919	CNVD
Neuroblastoma	21899760	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Esophageal cancer	20955586	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	CNVD
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
Cancer	20164919	CNVD
Breast cancer	21364760	CNVD
Mortal	21835882	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	21858162	CNVD
Schizophrenia	20967226	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Autism	22102821	CNVD
Neuroblastoma	19536264	CNVD
Schizophrenia	23813976	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Ewing''s sarcoma	18628472	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Rheumatoid arthritis	23223014	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ependymoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:7767 , 50 per page) page: 1 2 3 4 5 6 7 ... 156

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21803600-21820200	Weak transcription	K562	blood
2	chr14:21804400-21810800	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr14:21809200-21819800	Weak transcription	Fetal Intestine Small	intestine
4	chr14:21809600-21809800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
5	chr14:21809800-21819200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr14:21810600-21811200	Enhancers	HepG2	liver
7	chr14:21810800-21811000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr14:21810800-21811000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr14:21810800-21811800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
10	chr14:21810800-21812200	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr14:21811000-21811200	Enhancers	Primary T killer memory cells from peripheral blood	blood
12	chr14:21811000-21811400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr14:21811000-21811600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr14:21811200-21811400	Enhancers	Primary B cells from peripheral blood	blood
15	chr14:21811200-21811400	Enhancers	Primary T cells from cord blood	blood
16	chr14:21811200-21811400	Enhancers	Dnd41	blood
17	chr14:21811200-21811400	Active TSS	Osteobl	bone
18	chr14:21811200-21811600	Enhancers	Colon Smooth Muscle	Colon
19	chr14:21811200-21811600	Flanking Active TSS	HepG2	liver
20	chr14:21811200-21811800	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr14:21811200-21819200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
22	chr14:21811400-21811600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
23	chr14:21811400-21811600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr14:21811400-21818800	Weak transcription	Primary B cells from peripheral blood	blood
25	chr14:21811400-21819000	Weak transcription	Primary T cells from cord blood	blood
26	chr14:21811400-21819000	Weak transcription	Dnd41	blood
27	chr14:21811400-21819200	Weak transcription	Osteobl	bone
28	chr14:21811600-21811800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr14:21811600-21811800	Enhancers	Gastric	stomach
30	chr14:21811600-21818600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr14:21811600-21819000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
32	chr14:21811600-21819000	Weak transcription	HepG2	liver
33	chr14:21811600-21820000	Weak transcription	Colon Smooth Muscle	Colon
34	chr14:21811800-21812000	Enhancers	Monocytes-CD14+_RO01746	blood
35	chr14:21811800-21818800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
36	chr14:21811800-21818800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr14:21811800-21820200	Weak transcription	Gastric	stomach
38	chr14:21812000-21819000	Weak transcription	Monocytes-CD14+_RO01746	blood
39	chr14:21812200-21818800	Weak transcription	Primary monocytes fromperipheralblood	blood
40	chr14:21814600-21816000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr14:21814800-21815000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr14:21814800-21815000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr14:21815000-21815600	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr14:21815000-21816000	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr14:21815000-21816400	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr14:21815000-21819200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr14:21815000-21819800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr14:21815200-21815400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr14:21815200-21815600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr14:21815200-21815600	Enhancers	NHDF-Ad	bronchial

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