Variant report

Variant	nsv536603
Chromosome Location	chr3:81534364-81707800
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:81539705-81539945	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:81598568-81598974	K562	blood:	n/a	n/a
3	ATF1	chr3:81539694-81539966	K562	blood:	n/a	n/a
4	ATF1	chr3:81598619-81598832	K562	blood:	n/a	n/a
5	ATF2	chr3:81534486-81534931	GM12878	blood:	n/a	n/a
6	ATF2	chr3:81534488-81535060	GM12878	blood:	n/a	n/a
7	ATF2	chr3:81593386-81593921	GM12878	blood:	n/a	n/a
8	BACH1	chr3:81622912-81622914	K562	blood:	n/a	n/a
9	BATF	chr3:81534486-81534834	GM12878	blood:	n/a	n/a
10	BATF	chr3:81606915-81607180	GM12878	blood:	n/a	n/a
11	BATF	chr3:81534550-81535092	GM12878	blood:	n/a	n/a
12	BCL11A	chr3:81534515-81534856	GM12878	blood:	n/a	chr3:81534661-81534670
13	BCLAF1	chr3:81534447-81534951	GM12878	blood:	n/a	chr3:81534661-81534670 chr3:81534899-81534908
14	BHLHE40	chr3:81534564-81534857	GM12878	blood:	n/a	n/a
15	BHLHE40	chr3:81598621-81598872	K562	blood:	n/a	n/a
16	BRCA1	chr3:81693047-81693068	H1-hESC	embryonic stem cell:	n/a	n/a
17	CCNT2	chr3:81598585-81598820	K562	blood:	n/a	n/a
18	CCNT2	chr3:81689401-81689601	K562	blood:	n/a	n/a
19	CEBPB	chr3:81552187-81552422	A549	lung:	n/a	chr3:81552320-81552331
20	CEBPB	chr3:81552183-81552467	K562	blood:	n/a	chr3:81552320-81552331
21	CEBPB	chr3:81552175-81552736	IMR90	lung:	n/a	chr3:81552320-81552331
22	CEBPB	chr3:81539661-81540375	IMR90	lung:	n/a	n/a
23	CEBPB	chr3:81552175-81552499	HepG2	liver:	n/a	chr3:81552320-81552331
24	CEBPB	chr3:81539662-81540005	A549	lung:	n/a	n/a
25	CEBPB	chr3:81539619-81540135	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr3:81551436-81551739	A549	lung:	n/a	chr3:81551593-81551602 chr3:81551591-81551602 chr3:81551593-81551602 chr3:81551593-81551602 chr3:81551592-81551603 chr3:81551593-81551602 chr3:81551591-81551604 chr3:81551591-81551604
27	CEBPB	chr3:81621436-81621659	IMR90	lung:	n/a	chr3:81621520-81621531
28	CEBPB	chr3:81692035-81692347	HepG2	liver:	n/a	chr3:81692211-81692222
29	CEBPB	chr3:81651845-81651848	A549	lung:	n/a	n/a
30	CEBPB	chr3:81706978-81707231	Hela-S3	cervix:	n/a	chr3:81707091-81707102
31	CEBPB	chr3:81551436-81551788	HepG2	liver:	n/a	chr3:81551593-81551602 chr3:81551591-81551602 chr3:81551593-81551602 chr3:81551593-81551602 chr3:81551592-81551603 chr3:81551593-81551602 chr3:81551591-81551604 chr3:81551591-81551604
32	CEBPB	chr3:81539748-81539887	HepG2	liver:	n/a	n/a
33	CEBPB	chr3:81629067-81629224	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr3:81539651-81540009	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr3:81621463-81621652	K562	blood:	n/a	chr3:81621520-81621531
36	CEBPB	chr3:81539649-81540003	K562	blood:	n/a	n/a
37	CEBPB	chr3:81551428-81551732	MCF-7	breast:	n/a	chr3:81551593-81551602 chr3:81551591-81551602 chr3:81551593-81551602 chr3:81551593-81551602 chr3:81551592-81551603 chr3:81551593-81551602 chr3:81551591-81551604 chr3:81551591-81551604
38	CEBPB	chr3:81539622-81540059	MCF-7	breast:	n/a	n/a
39	CEBPB	chr3:81551428-81551786	IMR90	lung:	n/a	chr3:81551593-81551602 chr3:81551591-81551602 chr3:81551593-81551602 chr3:81551593-81551602 chr3:81551592-81551603 chr3:81551593-81551602 chr3:81551591-81551604 chr3:81551591-81551604
40	CEBPB	chr3:81690893-81691087	K562	blood:	n/a	n/a
41	CEBPB	chr3:81594909-81595089	A549	lung:	n/a	n/a
42	CEBPB	chr3:81551523-81551723	K562	blood:	n/a	chr3:81551593-81551602 chr3:81551591-81551602 chr3:81551593-81551602 chr3:81551593-81551602 chr3:81551592-81551603 chr3:81551593-81551602 chr3:81551591-81551604 chr3:81551591-81551604
43	CEBPB	chr3:81539673-81540024	HepG2	liver:	n/a	n/a
44	CEBPB	chr3:81594798-81595128	IMR90	lung:	n/a	n/a
45	CEBPB	chr3:81541084-81541642	IMR90	lung:	n/a	chr3:81541270-81541283
46	CEBPD	chr3:81598573-81598878	K562	blood:	n/a	n/a
47	CEBPD	chr3:81598505-81598878	K562	blood:	n/a	n/a
48	CREB1	chr3:81539601-81540135	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr3:81692980-81693130	HCFaa	heart:	n/a	n/a
50	CTCF	chr3:81539740-81539940	GM19238	blood:	n/a	chr3:81539812-81539825 chr3:81539810-81539826 chr3:81539809-81539827 chr3:81539812-81539825 chr3:81539814-81539822 chr3:81539811-81539832

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:81604026-81604076	ProgFib	skin:	n/a
2	chr3:81604026-81604076	Hela-S3	cervix:	n/a
3	chr3:81540527-81540577	BJ	skin:	n/a
4	chr3:81604026-81604076	GM12891	blood:	n/a
5	chr3:81540527-81540577	AG04450	lung:	fetal
6	chr3:81604026-81604076	HUVEC	blood vessel:	n/a
7	chr3:81604026-81604076	HCF	heart:	n/a
8	chr3:81604026-81604076	U87	brain:	n/a
9	chr3:81540527-81540577	NH-A	brain:	n/a
10	chr3:81604026-81604076	SK-N-MC	brain:	n/a
11	chr3:81540527-81540577	GM12891	blood:	n/a
12	chr3:81604026-81604076	AG09319	gingival:	n/a
13	chr3:81540527-81540577	ProgFib	skin:	n/a
14	chr3:81604026-81604076	AG04450	lung:	fetal
15	chr3:81604026-81604076	GM12892	blood:	n/a
16	chr3:81540527-81540577	T-47D	breast:	n/a
17	chr3:81540527-81540577	SAEC	small airway:	n/a
18	chr3:81604026-81604076	SKMC	muscle:	n/a
19	chr3:81604026-81604076	RPTEC	kidney:	n/a
20	chr3:81540527-81540577	Jurkat	blood:	n/a
21	chr3:81540527-81540577	SK-N-SH	brain:	n/a
22	chr3:81604026-81604076	PrEC	prostate:	n/a
23	chr3:81604026-81604076	HEEpiC	esophagus:	n/a
24	chr3:81604026-81604076	Hepatocyte	liver:	n/a
25	chr3:81604026-81604076	AG04449	skin:	fetal
26	chr3:81540527-81540577	A549	lung:	n/a
27	chr3:81540527-81540577	HCT-116	colon:	n/a
28	chr3:81540527-81540577	HPAEpiC	pulmonary alveolar:	n/a
29	chr3:81540527-81540577	CMK	blood:	n/a
30	chr3:81540527-81540577	MCF10A-Er-Src	breast:	n/a
31	chr3:81604026-81604076	HRPEpiC	eye:	n/a
32	chr3:81540527-81540577	HAEpiC	amniotic membrane:	n/a
33	chr3:81540527-81540577	PANC-1	pancreas:	n/a
34	chr3:81604026-81604076	PFSK-1	brain:	n/a
35	chr3:81604026-81604076	NB4	blood:	n/a
36	chr3:81540527-81540577	H1-hESC	embryonic stem cell:	embryo
37	chr3:81540527-81540577	HCF	heart:	n/a
38	chr3:81604026-81604076	HepG2	liver:	n/a
39	chr3:81604026-81604076	SK-N-SH	brain:	n/a
40	chr3:81540527-81540577	HIPEpiC	eye:	n/a
41	chr3:81540527-81540577	AoSMC	blood vessel:	n/a
42	chr3:81604026-81604076	ECC-1	luminal epithelium:	n/a
43	chr3:81540527-81540577	NHBE	bronchial:	n/a
44	chr3:81604026-81604076	HCT-116	colon:	n/a
45	chr3:81540527-81540577	HEK293	kidney:	embryo
46	chr3:81604026-81604076	HRE	kidney:	n/a
47	chr3:81540527-81540577	GM12892	blood:	n/a
48	chr3:81540527-81540577	AG09319	gingival:	n/a
49	chr3:81540527-81540577	HEEpiC	esophagus:	n/a
50	chr3:81604026-81604076	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:81630870..81631818-chr3:81692664..81693573,4	MCF-7	breast:
2	chr3:81468010..81468642-chr3:81539494..81540060,2	MCF-7	breast:
3	chr3:81538877..81541023-chr3:81682087..81685020,2	MCF-7	breast:
4	chr17:56735051..56736577-chr3:81662286..81664124,2	MCF-7	breast:
5	chr3:81660001..81661927-chr3:81662830..81664385,2	K562	blood:
6	chr3:81630870..81631818-chr3:81692664..81693573,4	MCF-7	breast:
7	chr3:81538965..81540197-chr3:81692644..81693504,4	MCF-7	breast:
8	chr3:81605753..81607787-chr3:81613884..81616486,2	MCF-7	breast:
9	chr12:104359580..104360355-chr3:81570763..81571263,2	NB4	blood:
10	chr3:81702517..81704180-chr3:81809893..81811884,2	K562	blood:
11	chr3:81652021..81654582-chr3:81671146..81673581,2	MCF-7	breast:
12	chr3:81468046..81468668-chr3:81630873..81631740,2	MCF-7	breast:
13	chr3:81630932..81631818-chr3:81692595..81693468,3	MCF-7	breast:
14	chr3:81652021..81654582-chr3:81671146..81673581,2	MCF-7	breast:
15	chr17:57120862..57121542-chr3:81600136..81600921,2	MCF-7	breast:
16	chr3:81350858..81351477-chr3:81692810..81693343,2	MCF-7	breast:
17	chr3:81607675..81609561-chr3:81976999..81978516,2	K562	blood:
18	chr3:81596549..81599236-chr3:81601556..81604295,2	K562	blood:
19	chr3:81609423..81612077-chr3:81612597..81614184,2	K562	blood:
20	chr3:81538877..81541023-chr3:81682087..81685020,2	MCF-7	breast:
21	chr3:81660001..81661927-chr3:81662830..81664385,2	K562	blood:
22	chr3:81630866..81631772-chr3:82182178..82183039,2	MCF-7	breast:
23	chr3:81673093..81675788-chr3:81810671..81812507,2	K562	blood:
24	chr3:81693699..81695612-chr3:81703909..81706890,2	MCF-7	breast:
25	chr3:81630932..81631818-chr3:81692595..81693468,3	MCF-7	breast:
26	chr3:81596549..81599236-chr3:81601556..81604295,2	K562	blood:
27	chr3:81605753..81607787-chr3:81613884..81616486,2	MCF-7	breast:
28	chr3:81609423..81612077-chr3:81612597..81614184,2	K562	blood:
29	chr3:81538965..81540197-chr3:81692644..81693504,4	MCF-7	breast:
30	chr3:81693699..81695612-chr3:81703909..81706890,2	MCF-7	breast:
31	chr3:81706649..81709647-chr3:81713380..81715113,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CADM2-8	chr3:81597025-81598649	NONHSAT090615
2	lnc-ROBO1-7	chr3:81703730-81704152	NONHSAT090617
3	lnc-CADM2-8	chr3:81597097-81598171	ENSG00000249130
4	lnc-CADM2-8	chr3:81598550-81598657	ENSG00000249130

Variant related genes	Relation type
ENSG00000240404	TF binding region
RNU2-28P	TF binding region
SETP6	TF binding region
GBE1	TF binding region
ENSG00000240404	CpG island
RNU2-28P	CpG island
SETP6	CpG island
GBE1	CpG island
ENSG00000114480	chromatin interactions
ENSG00000139372	chromatin interactions
KIAA1598	miRNA target sites
SLC25A22	miRNA target sites

Extended variants
information (count: 6069 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:6069 , 50 per page) page: 1 2 3 4 5 6 7 ... 122

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145983516	chr3:81534366-81534367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs560946694	chr3:81534409-81534410	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs139860257	chr3:81534434-81534435	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs184361434	chr3:81534438-81534439	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs543562410	chr3:81534488-81534489	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs59740898	chr3:81534547-81534548	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs532019802	chr3:81534592-81534593	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs552437722	chr3:81534596-81534597	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs143412866	chr3:81534654-81534655	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs144535544	chr3:81534671-81534672	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs548015897	chr3:81534673-81534674	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs567931249	chr3:81534736-81534737	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs536299362	chr3:81534747-81534748	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs549882620	chr3:81534784-81534785	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs11917116	chr3:81534829-81534830	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs114356998	chr3:81534894-81534895	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs559178803	chr3:81534917-81534918	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs6783132	chr3:81534944-81534945	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs535350146	chr3:81534955-81534956	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs820279	chr3:81534969-81534970	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs543836097	chr3:81534970-81534971	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs575108727	chr3:81535110-81535111	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs543960615	chr3:81535115-81535116	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs375900818	chr3:81535124-81535125	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs543509458	chr3:81535138-81535139	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs563274187	chr3:81535187-81535188	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs528071408	chr3:81535195-81535196	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs554536098	chr3:81535253-81535254	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs545528555	chr3:81535267-81535268	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs559588912	chr3:81535270-81535271	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs115755740	chr3:81535278-81535279	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs548081275	chr3:81535314-81535315	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs561516347	chr3:81535354-81535355	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs530632102	chr3:81535369-81535370	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs116808778	chr3:81535374-81535375	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs540542981	chr3:81535395-81535396	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs370833396	chr3:81535405-81535406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs7631196	chr3:81535450-81535451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs570077218	chr3:81535474-81535475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs114819285	chr3:81535483-81535484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs78822029	chr3:81535517-81535518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs566070548	chr3:81535524-81535525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs535309400	chr3:81535584-81535585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs560140977	chr3:81535606-81535607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs534643520	chr3:81535620-81535621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs373715246	chr3:81535630-81535631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs181487781	chr3:81535664-81535665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs375435706	chr3:81535692-81535693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557016547	chr3:81535703-81535704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs576906135	chr3:81535750-81535751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Melanoma	18172304	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Acute myeloid leukemia	20729466	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Colorectal cancer	16272173	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Soft tissue tumor	16732325	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Mental retardation	17124404	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Autism	20808228	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Urothelial carcinoma	21177765	CNVD

Chromatin state (count:1588 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:81528600-81534400	Weak transcription	HUVEC	blood vessel
2	chr3:81532400-81536800	Weak transcription	Right Atrium	heart
3	chr3:81532600-81540000	Weak transcription	Left Ventricle	heart
4	chr3:81532600-81540000	Weak transcription	Right Ventricle	heart
5	chr3:81533400-81534400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr3:81533400-81534600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr3:81533400-81535400	Enhancers	Fetal Lung	lung
8	chr3:81533600-81534400	Enhancers	Fetal Stomach	stomach
9	chr3:81533600-81534600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr3:81533600-81534600	Enhancers	NHDF-Ad	bronchial
11	chr3:81533600-81534800	Enhancers	Rectal Smooth Muscle	rectum
12	chr3:81533600-81534800	Enhancers	GM12878-XiMat	blood
13	chr3:81533600-81535000	Enhancers	Fetal Heart	heart
14	chr3:81533800-81534400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr3:81533800-81534600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr3:81533800-81534600	Enhancers	Adipose Nuclei	Adipose
17	chr3:81533800-81534600	Enhancers	Duodenum Smooth Muscle	Duodenum
18	chr3:81533800-81534600	Enhancers	Rectal Mucosa Donor 31	rectum
19	chr3:81533800-81534600	Enhancers	Skeletal Muscle Female	skeletal muscle
20	chr3:81533800-81534800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr3:81533800-81535000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr3:81533800-81535200	Enhancers	Psoas Muscle	Psoas
23	chr3:81533800-81535400	Enhancers	Colon Smooth Muscle	Colon
24	chr3:81533800-81535400	Enhancers	Osteobl	bone
25	chr3:81534000-81534600	Weak transcription	Aorta	Aorta
26	chr3:81534000-81534800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr3:81534000-81534800	Weak transcription	Ovary	ovary
28	chr3:81534000-81535200	Enhancers	Colonic Mucosa	Colon
29	chr3:81534000-81535200	Enhancers	NH-A	brain
30	chr3:81534000-81535400	Enhancers	Primary monocytes fromperipheralblood	blood
31	chr3:81534000-81535400	Enhancers	Skeletal Muscle Male	skeletal muscle
32	chr3:81534000-81547200	Weak transcription	Stomach Smooth Muscle	stomach
33	chr3:81534200-81534600	Weak transcription	Duodenum Mucosa	Duodenum
34	chr3:81534200-81535400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr3:81534200-81535400	Enhancers	Muscle Satellite Cultured Cells	--
36	chr3:81534400-81534600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr3:81534400-81534600	Enhancers	Monocytes-CD14+_RO01746	blood
38	chr3:81534400-81534800	Enhancers	HUVEC	blood vessel
39	chr3:81534400-81534800	Enhancers	NHLF	lung
40	chr3:81534400-81535000	Enhancers	HSMM	muscle
41	chr3:81534400-81535200	Enhancers	NHEK	skin
42	chr3:81534400-81535400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr3:81534600-81534800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
44	chr3:81534600-81534800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
45	chr3:81534600-81535000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr3:81534600-81535000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr3:81534600-81535000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr3:81534600-81535000	Active TSS	Duodenum Smooth Muscle	Duodenum
49	chr3:81534600-81535200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr3:81534600-81535200	Flanking Active TSS	Adipose Nuclei	Adipose

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