Variant report

Variant	nsv832841
Chromosome Location	chr14:81588322-81743921
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3272)
CpG islands
(count:1955)
Chromatin interactive
region (count:291)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3272 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:81636768-81637291	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:81735866-81736155	K562	blood:	n/a	n/a
3	ARID3A	chr14:81687484-81688039	K562	blood:	n/a	n/a
4	ARID3A	chr14:81678314-81678544	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:81718815-81718885	K562	blood:	n/a	n/a
6	ARID3A	chr14:81700788-81700851	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:81697909-81698198	HepG2	liver:	n/a	n/a
8	ARID3A	chr14:81663352-81663382	K562	blood:	n/a	n/a
9	ARID3A	chr14:81630534-81630855	HepG2	liver:	n/a	n/a
10	ARID3A	chr14:81687116-81687995	HepG2	liver:	n/a	n/a
11	ARID3A	chr14:81685621-81685821	K562	blood:	n/a	n/a
12	ARID3A	chr14:81689001-81689374	HepG2	liver:	n/a	n/a
13	ARID3A	chr14:81685039-81686068	HepG2	liver:	n/a	n/a
14	ARID3A	chr14:81636854-81637259	K562	blood:	n/a	n/a
15	ATF1	chr14:81630531-81630888	K562	blood:	n/a	n/a
16	ATF1	chr14:81687324-81688028	K562	blood:	n/a	n/a
17	ATF1	chr14:81685588-81685941	K562	blood:	n/a	chr14:81685744-81685758
18	ATF1	chr14:81629305-81629696	K562	blood:	n/a	n/a
19	ATF1	chr14:81734272-81734718	K562	blood:	n/a	n/a
20	ATF2	chr14:81687193-81687898	GM12878	blood:	n/a	n/a
21	ATF2	chr14:81686714-81687313	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr14:81686734-81687301	GM12878	blood:	n/a	n/a
23	ATF2	chr14:81685474-81686222	GM12878	blood:	n/a	chr14:81685744-81685758 chr14:81685746-81685757
24	ATF2	chr14:81685409-81686377	H1-hESC	embryonic stem cell:	n/a	chr14:81685744-81685758 chr14:81685746-81685757
25	ATF2	chr14:81588558-81589111	GM12878	blood:	n/a	n/a
26	ATF2	chr14:81588590-81589068	GM12878	blood:	n/a	n/a
27	ATF2	chr14:81687380-81687980	GM12878	blood:	n/a	n/a
28	ATF2	chr14:81701351-81701804	GM12878	blood:	n/a	n/a
29	ATF2	chr14:81636664-81637328	GM12878	blood:	n/a	n/a
30	ATF2	chr14:81686982-81688130	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF2	chr14:81636703-81637219	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF2	chr14:81701352-81701940	GM12878	blood:	n/a	n/a
33	ATF2	chr14:81685488-81686385	H1-hESC	embryonic stem cell:	n/a	chr14:81685744-81685758 chr14:81685746-81685757
34	ATF2	chr14:81687333-81687952	H1-hESC	embryonic stem cell:	n/a	n/a
35	ATF2	chr14:81685411-81686452	GM12878	blood:	n/a	chr14:81685744-81685758 chr14:81685746-81685757
36	ATF2	chr14:81675515-81675881	GM12878	blood:	n/a	n/a
37	ATF3	chr14:81687335-81687839	HepG2	liver:	n/a	n/a
38	ATF3	chr14:81687326-81687855	HepG2	liver:	n/a	n/a
39	ATF3	chr14:81630463-81630829	K562	blood:	n/a	chr14:81630498-81630512
40	ATF3	chr14:81636861-81637312	K562	blood:	n/a	n/a
41	ATF3	chr14:81687331-81687893	K562	blood:	n/a	n/a
42	ATF3	chr14:81687382-81687950	H1-hESC	embryonic stem cell:	n/a	n/a
43	ATF3	chr14:81687271-81687881	A549	lung:	n/a	n/a
44	ATF3	chr14:81685427-81686110	A549	lung:	n/a	chr14:81685746-81685757 chr14:81685745-81685755 chr14:81685745-81685758 chr14:81685746-81685757 chr14:81685742-81685756 chr14:81685744-81685757
45	ATF3	chr14:81687289-81687959	GM12878	blood:	n/a	n/a
46	ATF3	chr14:81629425-81629605	K562	blood:	n/a	n/a
47	ATF3	chr14:81685521-81686066	A549	lung:	n/a	chr14:81685746-81685757 chr14:81685745-81685755 chr14:81685745-81685758 chr14:81685746-81685757 chr14:81685742-81685756 chr14:81685744-81685757
48	BACH1	chr14:81687580-81688500	K562	blood:	n/a	n/a
49	BACH1	chr14:81686878-81688305	H1-hESC	embryonic stem cell:	n/a	n/a
50	BACH1	chr14:81636887-81637203	K562	blood:	n/a	n/a

(count:1955 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:81649681-81649731	HNPCEpiC	eye:	n/a
2	chr14:81688339-81688389	CMK	blood:	n/a
3	chr14:81686396-81686446	HPAEpiC	pulmonary alveolar:	n/a
4	chr14:81649681-81649731	HNPCEpiC	eye:	n/a
5	chr14:81688339-81688389	CMK	blood:	n/a
6	chr14:81686396-81686446	HPAEpiC	pulmonary alveolar:	n/a
7	chr14:81690541-81690591	NH-A	brain:	n/a
8	chr14:81687766-81687816	Hela-S3	cervix:	n/a
9	chr14:81690541-81690591	SK-N-SH	brain:	n/a
10	chr14:81688436-81688486	MCF-7	breast:	n/a
11	chr14:81687884-81687934	H1-hESC	embryonic stem cell:	embryo
12	chr14:81687959-81688009	HRCEpiC	kidney:	n/a
13	chr14:81687884-81687934	HEEpiC	esophagus:	n/a
14	chr14:81687884-81687934	HIPEpiC	eye:	n/a
15	chr14:81685593-81685643	HL-60	blood:	n/a
16	chr14:81609917-81609967	NHBE	bronchial:	n/a
17	chr14:81688436-81688486	GM19239	blood:	n/a
18	chr14:81686857-81686907	SK-N-SH_RA	brain:	n/a
19	chr14:81687766-81687816	GM12878	blood:	n/a
20	chr14:81686966-81687016	AG10803	skin:	n/a
21	chr14:81687884-81687934	ECC-1	luminal epithelium:	n/a
22	chr14:81690541-81690591	AG09309	skin:	n/a
23	chr14:81636615-81636665	NT2-D1	testis:	n/a
24	chr14:81687645-81687695	AG04449	skin:	fetal
25	chr14:81685801-81685851	LNCaP	prostate:	n/a
26	chr14:81609977-81610027	LNCaP	prostate:	n/a
27	chr14:81686396-81686446	SKMC	muscle:	n/a
28	chr14:81686781-81686831	GM12891	blood:	n/a
29	chr14:81686966-81687016	NHDF-neo	bronchial:	n/a
30	chr14:81702510-81702560	SK-N-MC	brain:	n/a
31	chr14:81687645-81687695	AG09309	skin:	n/a
32	chr14:81687645-81687695	HRE	kidney:	n/a
33	chr14:81685593-81685643	ECC-1	luminal epithelium:	n/a
34	chr14:81610002-81610052	Jurkat	blood:	n/a
35	chr14:81687124-81687174	HepG2	liver:	n/a
36	chr14:81687483-81687533	NHBE	bronchial:	n/a
37	chr14:81686232-81686282	ECC-1	luminal epithelium:	n/a
38	chr14:81686966-81687016	SAEC	small airway:	n/a
39	chr14:81686966-81687016	Hepatocyte	liver:	n/a
40	chr14:81686396-81686446	AoSMC	blood vessel:	n/a
41	chr14:81610002-81610052	SK-N-MC	brain:	n/a
42	chr14:81688436-81688486	NH-A	brain:	n/a
43	chr14:81687884-81687934	HRE	kidney:	n/a
44	chr14:81688339-81688389	LNCaP	prostate:	n/a
45	chr14:81687754-81687804	AG04450	lung:	fetal
46	chr14:81685801-81685851	Hepatocyte	liver:	n/a
47	chr14:81682983-81683033	HRE	kidney:	n/a
48	chr14:81687124-81687174	LNCaP	prostate:	n/a
49	chr14:81687491-81687541	HCPEpiC	choroid plexus:	n/a
50	chr14:81610812-81610862	HRCEpiC	kidney:	n/a

(count:291 , 50 per page) page: 1 2 3 4 5 6

No.	Distal block	Cell Line	Cell type
1	chr14:81644138..81645856-chr14:81700213..81702978,2	K562	blood:
2	chr14:81686710..81687631-chr16:30076754..30077254,2	NB4	blood:
3	chr14:81685497..81686123-chr17:56736217..56736921,2	MCF-7	breast:
4	chr14:81686752..81687294-chr15:75287631..75288229,2	NB4	blood:
5	chr14:81628909..81631535-chr14:81690174..81692139,2	MCF-7	breast:
6	chr14:81692029..81695563-chr14:81697137..81699977,3	K562	blood:
7	chr14:81686902..81687551-chr16:3207373..3208030,2	MCF-7	breast:
8	chr14:81686696..81687404-chr16:3070201..3071106,2	Hela-S3	cervix:
9	chr14:81634129..81641173-chr14:81683190..81688873,17	MCF-7	breast:
10	chr14:81686299..81687927-chr14:81738274..81739791,2	MCF-7	breast:
11	chr14:81684235..81687113-chr14:81978214..81980524,2	MCF-7	breast:
12	chr14:81610260..81612495-chr14:81613235..81615215,2	K562	blood:
13	chr14:81447196..81448849-chr14:81635444..81638287,2	MCF-7	breast:
14	chr14:81685904..81686476-chr5:119526721..119527705,2	NB4	blood:
15	chr14:81651257..81653411-chr14:81683481..81686410,2	MCF-7	breast:
16	chr14:81682072..81683582-chr14:81925884..81928192,2	MCF-7	breast:
17	chr14:81645137..81647091-chr14:81650122..81652233,2	K562	blood:
18	chr14:81644106..81646643-chr14:81658404..81660204,2	MCF-7	breast:
19	chr14:81685770..81687296-chr14:81799417..81802268,2	K562	blood:
20	chr14:81683547..81687186-chr14:81935321..81938414,4	K562	blood:
21	chr14:81643515..81648900-chr14:81684307..81689030,7	K562	blood:
22	chr11:62607847..62610429-chr14:81685823..81688377,2	MCF-7	breast:
23	chr14:81644106..81646643-chr14:81658404..81660204,2	MCF-7	breast:
24	chr14:81684506..81688423-chr14:81892845..81897193,10	K562	blood:
25	chr14:81617947..81620851-chr14:81684771..81687326,2	MCF-7	breast:
26	chr14:81735524..81736431-chr14:81930547..81931469,5	MCF-7	breast:
27	chr14:81686241..81688749-chr14:81701998..81704279,2	K562	blood:
28	chr14:81316288..81318355-chr14:81684357..81686706,2	K562	blood:
29	chr14:81421307..81423560-chr14:81685821..81687772,2	MCF-7	breast:
30	chr14:81719518..81722167-chr14:81734780..81736753,2	K562	blood:
31	chr14:81686865..81688853-chr14:81734736..81736756,2	K562	blood:
32	chr14:81685898..81688626-chr14:81711867..81715225,3	K562	blood:
33	chr14:81616498..81618878-chr14:81620802..81623357,2	K562	blood:
34	chr14:81651257..81653411-chr14:81683481..81686410,2	MCF-7	breast:
35	chr14:81645137..81647091-chr14:81650122..81652233,2	K562	blood:
36	chr14:81684227..81690291-chr14:81911956..81927827,27	MCF-7	breast:
37	chr14:81686424..81687263-chr17:57917645..57918362,2	Hela-S3	cervix:
38	chr14:81629067..81632213-chr14:81683312..81688169,7	K562	blood:
39	chr14:81691775..81692400-chr14:81703764..81704509,2	MCF-7	breast:
40	chr14:81686690..81687670-chr16:2802490..2803160,2	Hela-S3	cervix:
41	chr14:81688918..81692006-chr14:81697199..81699936,3	K562	blood:
42	chr14:81684973..81687245-chr14:81740036..81742167,2	K562	blood:
43	chr14:81606418..81608922-chr14:81611798..81613864,2	MCF-7	breast:
44	chr14:81684973..81687245-chr14:81740036..81742167,2	K562	blood:
45	chr14:81647686..81650322-chr14:81684054..81687029,2	MCF-7	breast:
46	chr14:81685803..81688081-chr17:62223378..62225189,2	MCF-7	breast:
47	chr14:81728442..81730131-chr14:81732083..81734711,2	K562	blood:
48	chr14:81685671..81687321-chr14:81879290..81881702,3	MCF-7	breast:
49	chr14:81656301..81665753-chr14:81684174..81688927,14	MCF-7	breast:
50	chr14:81634129..81641173-chr14:81683190..81688873,17	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TSHR-2	chr14:81687723-81689737	NONHSAT038056
2	lnc-GTF2A1-3	chr14:81624841-81625100	NONHSAT038050
3	lnc-TSHR-2	chr14:81688420-81689753	NONHSAT038057
4	lnc-TSHR-2	chr14:81687983-81688799	ENSG00000247694
5	lnc-STON2-5	chr14:81641799-81645528	NONHSAT038052
6	lnc-GTF2A1-1	chr14:81636453-81636758	ENSG00000258999.1
7	lnc-TSHR-2	chr14:81687562-81687869	ENSG00000247694
8	lnc-GTF2A1-3	chr14:81625692-81625723	NONHSAT038050
9	lnc-GTF2A1-1	chr14:81631537-81631725	ENSG00000258999.1
10	lnc-STON2-2	chr14:81725909-81726583	NONHSAT038061

No data

Variant related genes	Relation type
DYNLL1P1	TF binding region
SNORA79	TF binding region
UNGP3	TF binding region
ENSG00000258999	TF binding region
GTF2A1	TF binding region
STON2	TF binding region
DYNLL1P1	CpG island
SNORA79	CpG island
UNGP3	CpG island
ENSG00000258999	CpG island
GTF2A1	CpG island
STON2	CpG island
ENSG00000214941	chromatin interactions
ENSG00000255242	chromatin interactions
ENSG00000270343	chromatin interactions
ENSG00000268230	chromatin interactions
ENSG00000196542	chromatin interactions
ENSG00000258675	chromatin interactions
ENSG00000140577	chromatin interactions
ENSG00000272426	chromatin interactions
ENSG00000059588	chromatin interactions
ENSG00000242163	chromatin interactions
ENSG00000182325	chromatin interactions
ENSG00000166012	chromatin interactions
ENSG00000138386	chromatin interactions
ENSG00000172239	chromatin interactions
ENSG00000174586	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000132024	chromatin interactions
ENSG00000165409	chromatin interactions
ENSG00000205913	chromatin interactions
ENSG00000269054	chromatin interactions
ENSG00000127995	chromatin interactions
ENSG00000131944	chromatin interactions
ENSG00000124659	chromatin interactions
ENSG00000100632	chromatin interactions
ENSG00000221303	chromatin interactions
ENSG00000175193	chromatin interactions
ENSG00000108312	chromatin interactions
ENSG00000272273	chromatin interactions
ENSG00000169228	chromatin interactions
ENSG00000122643	chromatin interactions
ENSG00000167978	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000132016	chromatin interactions
ENSG00000163584	chromatin interactions
ENSG00000068697	chromatin interactions
ENSG00000149925	chromatin interactions
ENSG00000101144	chromatin interactions
ENSG00000103253	chromatin interactions
ENSG00000170468	chromatin interactions
ENSG00000185803	chromatin interactions
ENSG00000165417	chromatin interactions
ENSG00000140022	chromatin interactions
ENSG00000073008	chromatin interactions
ENSG00000160753	chromatin interactions
ENSG00000223734	chromatin interactions
ENSG00000102786	chromatin interactions
ENSG00000126247	chromatin interactions
ENSG00000029364	chromatin interactions
ENSG00000258999	chromatin interactions
ENSG00000273247	chromatin interactions
ENSG00000261717	chromatin interactions
ENSG00000230658	chromatin interactions
ENSG00000113448	chromatin interactions
ENSG00000130935	chromatin interactions
ENSG00000206652	chromatin interactions
ENSG00000222724	chromatin interactions
ENSG00000258915	chromatin interactions
ENSG00000100629	chromatin interactions
ENSG00000169230	chromatin interactions
ENSG00000172007	chromatin interactions
ENSG00000178741	chromatin interactions
ENSG00000137312	chromatin interactions
ENSG00000011295	chromatin interactions
ENSG00000130816	chromatin interactions
ENSG00000258605	chromatin interactions
ENSG00000042429	chromatin interactions
ENSG00000198794	chromatin interactions
ENSG00000225855	chromatin interactions
ENSG00000199753	chromatin interactions
ENSG00000166822	chromatin interactions
ENSG00000255717	chromatin interactions
ENSG00000261889	chromatin interactions
ENSG00000006327	chromatin interactions
ENSG00000071537	chromatin interactions
ENSG00000122550	chromatin interactions
ENSG00000174579	chromatin interactions
ENSG00000123552	chromatin interactions
ENSG00000266402	chromatin interactions
ENSG00000132475	chromatin interactions
ENSG00000108821	chromatin interactions
ENSG00000121289	chromatin interactions
ENSG00000205579	chromatin interactions
ENSG00000198668	chromatin interactions
ENSG00000178718	chromatin interactions
TAF5	miRNA target sites
TPRG1L	miRNA target sites

Extended variants
information (count: 5500 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:5500 , 50 per page) page: 1 2 3 4 5 6 7 ... 110

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113866322	chr14:81588469-81588470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs112216322	chr14:81588480-81588481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs576932996	chr14:81588531-81588532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs146041395	chr14:81588577-81588578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs79880793	chr14:81588625-81588626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs529746762	chr14:81588650-81588651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs542057880	chr14:81588667-81588668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs149254985	chr14:81588677-81588678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs73340239	chr14:81588717-81588718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs76640206	chr14:81588719-81588720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs570386467	chr14:81588721-81588722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs182517799	chr14:81588752-81588753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs528498884	chr14:81588793-81588794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs546578520	chr14:81588814-81588815	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs56369010	chr14:81588915-81588916	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs55993259	chr14:81588958-81588959	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs187742508	chr14:81588983-81588984	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs56306987	chr14:81588995-81588996	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs539993229	chr14:81589009-81589010	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs12891616	chr14:81589014-81589015	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs566351229	chr14:81589129-81589130	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs573564639	chr14:81589160-81589161	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs541071597	chr14:81589200-81589201	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs372799225	chr14:81589202-81589203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs553003834	chr14:81589207-81589208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs543505587	chr14:81589240-81589241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs192415372	chr14:81589295-81589296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs144419918	chr14:81589301-81589302	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs7155361	chr14:81589333-81589334	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs575372552	chr14:81589407-81589408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs184701845	chr14:81589446-81589447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs3783940	chr14:81589451-81589452	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs528367117	chr14:81589452-81589453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs113220562	chr14:81589461-81589462	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs546443279	chr14:81589464-81589465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs187059451	chr14:81589465-81589466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs548347716	chr14:81589466-81589467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs199951264	chr14:81589472-81589473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs200937806	chr14:81589473-81589474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs566727144	chr14:81589477-81589478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs397840462	chr14:81589485-81589486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs61351357	chr14:81589486-81589487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs569310787	chr14:81589535-81589536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs377335179	chr14:81589551-81589552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs192068089	chr14:81589562-81589563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs184422528	chr14:81589587-81589588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs534502652	chr14:81589607-81589608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs151093829	chr14:81589703-81589704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs76213566	chr14:81589794-81589795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs8019356	chr14:81589806-81589807	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:66)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3385 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:81538200-81593000	Weak transcription	Psoas Muscle	Psoas
2	chr14:81572600-81591400	Weak transcription	Liver	Liver
3	chr14:81579800-81591800	Weak transcription	Thymus	Thymus
4	chr14:81579800-81591800	Weak transcription	Dnd41	blood
5	chr14:81581000-81593200	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr14:81586400-81589800	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr14:81586800-81592200	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr14:81587400-81588800	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr14:81587800-81589400	Enhancers	Primary B cells from peripheral blood	blood
10	chr14:81587800-81589800	Weak transcription	Primary B cells from cord blood	blood
11	chr14:81588600-81589600	Enhancers	GM12878-XiMat	blood
12	chr14:81588800-81589200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
13	chr14:81589200-81589800	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr14:81589400-81592000	Weak transcription	Primary B cells from peripheral blood	blood
15	chr14:81589600-81589800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr14:81589800-81590000	Enhancers	Primary B cells from cord blood	blood
17	chr14:81589800-81590200	Weak transcription	Primary monocytes fromperipheralblood	blood
18	chr14:81589800-81590600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
19	chr14:81590000-81592000	Weak transcription	Primary B cells from cord blood	blood
20	chr14:81590200-81591200	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr14:81590400-81590600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr14:81590600-81593200	Enhancers	Monocytes-CD14+_RO01746	blood
23	chr14:81590800-81593200	Weak transcription	Skeletal Muscle Female	skeletal muscle
24	chr14:81591200-81591600	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr14:81591400-81592200	Strong transcription	Liver	Liver
26	chr14:81591600-81592200	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr14:81591800-81592000	Weak transcription	Pancreas	Pancrea
28	chr14:81591800-81592200	ZNF genes & repeats	Thymus	Thymus
29	chr14:81591800-81592200	ZNF genes & repeats	GM12878-XiMat	blood
30	chr14:81591800-81592400	Strong transcription	Dnd41	blood
31	chr14:81592000-81592200	Enhancers	Primary B cells from cord blood	blood
32	chr14:81592000-81592200	Enhancers	Left Ventricle	heart
33	chr14:81592000-81592200	Enhancers	Pancreas	Pancrea
34	chr14:81592000-81592400	Enhancers	Primary B cells from peripheral blood	blood
35	chr14:81592200-81593400	Weak transcription	Primary neutrophils fromperipheralblood	blood
36	chr14:81592200-81593600	Weak transcription	Primary monocytes fromperipheralblood	blood
37	chr14:81592200-81597800	Weak transcription	Liver	Liver
38	chr14:81592200-81609000	Weak transcription	Thymus	Thymus
39	chr14:81592400-81601000	Weak transcription	Dnd41	blood
40	chr14:81593200-81594600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
41	chr14:81593400-81594800	Enhancers	Primary neutrophils fromperipheralblood	blood
42	chr14:81593600-81595200	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr14:81594600-81596000	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr14:81597800-81600200	Enhancers	Liver	Liver
45	chr14:81598000-81599800	Enhancers	Fetal Brain Female	brain
46	chr14:81598800-81599400	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr14:81599200-81600200	Enhancers	Fetal Brain Male	brain
48	chr14:81600200-81611000	Weak transcription	Liver	Liver
49	chr14:81600800-81609400	Weak transcription	Fetal Thymus	thymus
50	chr14:81601400-81603600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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