Variant report

Variant	nsv508315
Chromosome Location	chr1:77040085-77134730
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	ATF1	chr1:77119453-77119559	K562	blood:	n/a	n/a
2	BACH1	chr1:77046543-77046571	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr1:77048933-77049239	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr1:77133723-77134000	GM12878	blood:	n/a	n/a
5	BHLHE40	chr1:77112842-77112874	K562	blood:	n/a	n/a
6	CEBPB	chr1:77105851-77106102	IMR90	lung:	n/a	n/a
7	CEBPB	chr1:77105633-77106254	HCT-116	colon:	n/a	n/a
8	CEBPB	chr1:77052571-77052897	HepG2	liver:	n/a	chr1:77052721-77052732
9	CEBPB	chr1:77105688-77106193	HCT-116	colon:	n/a	n/a
10	CEBPB	chr1:77052547-77052850	A549	lung:	n/a	chr1:77052721-77052732
11	CEBPB	chr1:77049031-77049343	HepG2	liver:	n/a	chr1:77049192-77049203
12	CEBPB	chr1:77055199-77055448	A549	lung:	n/a	chr1:77055290-77055301
13	CEBPB	chr1:77048891-77049375	H1-hESC	embryonic stem cell:	n/a	chr1:77049192-77049203
14	CEBPB	chr1:77055136-77055460	HepG2	liver:	n/a	chr1:77055290-77055301
15	CEBPB	chr1:77052581-77052874	IMR90	lung:	n/a	chr1:77052721-77052732
16	CHD2	chr1:77048889-77049131	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr1:77086183-77086340	Medullo	brain:	n/a	n/a
18	CTCF	chr1:77054380-77054530	SK-N-SH_RA	brain:	n/a	n/a
19	CTCF	chr1:77071401-77071482	GM20000	blood:	n/a	n/a
20	CTCF	chr1:77086180-77086330	WERI-Rb-1	eye:	n/a	n/a
21	CTCF	chr1:77123600-77123750	GM12868	blood:	n/a	n/a
22	CTCF	chr1:77080298-77080363	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr1:77086260-77086410	WERI-Rb-1	eye:	n/a	n/a
24	CUX1	chr1:77097624-77097705	GM12878	blood:	n/a	n/a
25	E2F4	chr1:77105799-77106420	MCF10A-Er-Src	breast:	n/a	n/a
26	E2F4	chr1:77085334-77085714	MCF10A-Er-Src	breast:	n/a	n/a
27	E2F4	chr1:77082607-77082744	MCF10A-Er-Src	breast:	n/a	n/a
28	E2F4	chr1:77104220-77104525	MCF10A-Er-Src	breast:	n/a	n/a
29	EBF1	chr1:77133804-77133995	GM12878	blood:	n/a	n/a
30	EP300	chr1:77133917-77133958	GM12878	blood:	n/a	n/a
31	EP300	chr1:77093427-77093856	SK-N-SH_RA	brain:	n/a	n/a
32	EP300	chr1:77054390-77054803	SK-N-SH_RA	brain:	n/a	n/a
33	EP300	chr1:77125392-77125593	SK-N-SH_RA	brain:	n/a	chr1:77125510-77125519
34	EP300	chr1:77048909-77049228	H1-hESC	embryonic stem cell:	n/a	chr1:77049125-77049134
35	EP300	chr1:77042642-77044780	SK-N-SH	brain:	n/a	chr1:77044036-77044044
36	EP300	chr1:77053860-77055190	SK-N-SH	brain:	n/a	chr1:77054125-77054139
37	EP300	chr1:77043188-77043490	SK-N-SH_RA	brain:	n/a	n/a
38	EP300	chr1:77133744-77134055	GM12878	blood:	n/a	n/a
39	EP300	chr1:77042926-77043790	SK-N-SH_RA	brain:	n/a	n/a
40	EP300	chr1:77124920-77125136	SK-N-SH_RA	brain:	n/a	n/a
41	EP300	chr1:77093404-77093731	SK-N-SH_RA	brain:	n/a	n/a
42	EP300	chr1:77133699-77134142	GM12878	blood:	n/a	n/a
43	EP300	chr1:77124854-77125223	SK-N-SH_RA	brain:	n/a	n/a
44	EP300	chr1:77125379-77125648	SK-N-SH_RA	brain:	n/a	chr1:77125510-77125519
45	EP300	chr1:77124730-77125727	SK-N-SH	brain:	n/a	chr1:77125510-77125519
46	FOS	chr1:77050307-77050516	MCF10A-Er-Src	breast:	n/a	chr1:77050397-77050405 chr1:77050395-77050402 chr1:77050398-77050405
47	FOS	chr1:77049711-77049737	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr1:77101262-77101931	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr1:77125427-77125557	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr1:77105750-77106248	MCF10A-Er-Src	breast:	n/a	chr1:77106081-77106091 chr1:77105932-77105939 chr1:77105931-77105941 chr1:77105932-77105940 chr1:77106081-77106091 chr1:77105931-77105941 chr1:77105931-77105941 chr1:77105932-77105940 chr1:77105931-77105941

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:77042560-77042610	SKMC	muscle:	n/a
2	chr1:77043128-77043178	SKMC	muscle:	n/a
3	chr1:77049380-77049430	SK-N-SH	brain:	n/a
4	chr1:77096137-77096187	HUVEC	blood vessel:	n/a
5	chr1:77049380-77049430	HAEpiC	amniotic membrane:	n/a
6	chr1:77096137-77096187	PANC-1	pancreas:	n/a
7	chr1:77043128-77043178	A549	lung:	n/a
8	chr1:77096137-77096187	SKMC	muscle:	n/a
9	chr1:77043128-77043178	SK-N-SH	brain:	n/a
10	chr1:77043128-77043178	AG04450	lung:	fetal
11	chr1:77096137-77096187	ProgFib	skin:	n/a
12	chr1:77042560-77042610	ovcar-3	ovarian:	n/a
13	chr1:77042560-77042610	HPAEpiC	pulmonary alveolar:	n/a
14	chr1:77042560-77042610	HRCEpiC	kidney:	n/a
15	chr1:77049380-77049430	NHBE	bronchial:	n/a
16	chr1:77043128-77043178	SK-N-SH_RA	brain:	n/a
17	chr1:77043128-77043178	GM12891	blood:	n/a
18	chr1:77042560-77042610	ProgFib	skin:	n/a
19	chr1:77043128-77043178	PrEC	prostate:	n/a
20	chr1:77043128-77043178	HRCEpiC	kidney:	n/a
21	chr1:77049380-77049430	BJ	skin:	n/a
22	chr1:77043128-77043178	MCF10A-Er-Src	breast:	n/a
23	chr1:77043128-77043178	HEK293	kidney:	embryo
24	chr1:77096137-77096187	IMR90	lung:	fetal
25	chr1:77049380-77049430	IMR90	lung:	fetal
26	chr1:77049380-77049430	Hela-S3	cervix:	n/a
27	chr1:77043128-77043178	GM06990	blood:	n/a
28	chr1:77096137-77096187	BJ	skin:	n/a
29	chr1:77042560-77042610	PrEC	prostate:	n/a
30	chr1:77096137-77096187	HAEpiC	amniotic membrane:	n/a
31	chr1:77049380-77049430	HCT-116	colon:	n/a
32	chr1:77096137-77096187	U87	brain:	n/a
33	chr1:77042560-77042610	GM12892	blood:	n/a
34	chr1:77043128-77043178	NH-A	brain:	n/a
35	chr1:77043128-77043178	HCPEpiC	choroid plexus:	n/a
36	chr1:77049380-77049430	AG04449	skin:	fetal
37	chr1:77043128-77043178	ovcar-3	ovarian:	n/a
38	chr1:77043128-77043178	HRPEpiC	eye:	n/a
39	chr1:77049380-77049430	CMK	blood:	n/a
40	chr1:77042560-77042610	AG09319	gingival:	n/a
41	chr1:77049380-77049430	BE2_C	brain:	n/a
42	chr1:77042560-77042610	HUVEC	blood vessel:	n/a
43	chr1:77049380-77049430	SK-N-MC	brain:	n/a
44	chr1:77042560-77042610	MCF10A-Er-Src	breast:	n/a
45	chr1:77042560-77042610	SK-N-SH_RA	brain:	n/a
46	chr1:77042560-77042610	NHDF-neo	bronchial:	n/a
47	chr1:77096137-77096187	A549	lung:	n/a
48	chr1:77049380-77049430	MCF10A-Er-Src	breast:	n/a
49	chr1:77043128-77043178	IMR90	lung:	fetal
50	chr1:77049380-77049430	HCPEpiC	choroid plexus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:77076114..77078249-chr1:77109036..77110684,2	MCF-7	breast:
2	chr1:77076114..77078249-chr1:77109036..77110684,2	MCF-7	breast:
3	chr1:77056837..77059200-chr1:77061368..77063126,2	K562	blood:
4	chr1:77056837..77059200-chr1:77061368..77063126,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ST6GALNAC3-3	chr1:77102562-77103024	ENSG00000272855.1

Variant related genes	Relation type
ENSG00000272855	TF binding region
ENSG00000272855	CpG island

Extended variants
information (count: 2552 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:2552 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs78459640	chr1:77040089-77040090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs569884365	chr1:77040094-77040095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs183999980	chr1:77040175-77040176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs537323867	chr1:77040183-77040184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs436806	chr1:77040188-77040189	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs76746943	chr1:77040208-77040209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs187767870	chr1:77040211-77040212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs534771761	chr1:77040226-77040227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs553107861	chr1:77040235-77040236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs536683511	chr1:77040440-77040441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs571316867	chr1:77040470-77040471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs190729090	chr1:77040536-77040537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs556901695	chr1:77040546-77040547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs575103164	chr1:77040626-77040627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs542927901	chr1:77040736-77040737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs554801483	chr1:77040739-77040740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs146328283	chr1:77040750-77040751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs540421287	chr1:77040762-77040763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs565273673	chr1:77040763-77040764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs532621329	chr1:77040790-77040791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs544305840	chr1:77040839-77040840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs562924385	chr1:77040847-77040848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs556262092	chr1:77040890-77040891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs373902316	chr1:77040915-77040916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs377584217	chr1:77040922-77040923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs182874547	chr1:77040947-77040948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs549309785	chr1:77040984-77040985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs7536613	chr1:77041013-77041014	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs139389055	chr1:77041075-77041076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs115194213	chr1:77041089-77041090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs143334217	chr1:77041103-77041104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs150475571	chr1:77041105-77041106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs315026	chr1:77041173-77041174	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs376852854	chr1:77041211-77041212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs565140655	chr1:77041221-77041222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs568842773	chr1:77041290-77041291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs138274116	chr1:77041303-77041304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs554887282	chr1:77041364-77041365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs187221789	chr1:77041365-77041366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs192901785	chr1:77041376-77041377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs315027	chr1:77041382-77041383	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs182670671	chr1:77041454-77041455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs530308830	chr1:77041457-77041458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201974818	chr1:77041516-77041517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs11162180	chr1:77041553-77041554	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs562804085	chr1:77041555-77041556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs547413834	chr1:77041570-77041571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs562461509	chr1:77041585-77041586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs542241937	chr1:77041619-77041620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs187797709	chr1:77041645-77041646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Bladder cancer	21909424	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:257 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:77037400-77048400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr1:77038800-77042200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr1:77042200-77042400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr1:77042200-77043600	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr1:77042400-77042800	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr1:77042400-77043000	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr1:77042400-77043000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr1:77042400-77043400	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr1:77042600-77043800	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr1:77042800-77045800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr1:77043000-77043600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr1:77043000-77045800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr1:77043400-77044000	Enhancers	Pancreatic Islets	Pancreatic Islet
14	chr1:77043400-77045800	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr1:77043600-77045800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr1:77043600-77048000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr1:77043800-77045600	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr1:77044000-77051800	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr1:77045600-77046800	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr1:77045800-77046400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr1:77045800-77046400	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr1:77045800-77046600	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr1:77045800-77046600	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr1:77045800-77046800	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr1:77045800-77049800	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr1:77045800-77050600	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr1:77046200-77046600	Enhancers	H1 Cell Line	embryonic stem cell
28	chr1:77046400-77048000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr1:77046600-77048000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr1:77046600-77048400	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr1:77046600-77048600	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr1:77046800-77048000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr1:77046800-77048200	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr1:77047800-77050600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr1:77048000-77048200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr1:77048000-77049200	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr1:77048000-77049600	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr1:77048000-77050200	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr1:77048000-77050200	Enhancers	H9 Cell Line	embryonic stem cell
40	chr1:77048200-77048600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr1:77048200-77049200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr1:77048200-77050200	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr1:77048400-77049600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr1:77048400-77049800	Enhancers	H1 Cell Line	embryonic stem cell
45	chr1:77048600-77049400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr1:77048600-77049800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr1:77048600-77050200	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr1:77049000-77049600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr1:77049200-77049400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
50	chr1:77049200-77052600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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