Variant report

Variant	nsv1006776
Chromosome Location	chr1:76777323-76899975
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	chr1:76796829-76797028	K562	blood:	n/a	n/a
2	CBX3	chr1:76796545-76797128	HCT-116	colon:	n/a	n/a
3	CCNT2	chr1:76877130-76877206	K562	blood:	n/a	n/a
4	CEBPB	chr1:76796637-76797003	A549	lung:	n/a	n/a
5	CEBPB	chr1:76785035-76785336	A549	lung:	n/a	chr1:76785133-76785144
6	CEBPB	chr1:76892461-76892516	A549	lung:	n/a	n/a
7	CEBPB	chr1:76796692-76797006	MCF-7	breast:	n/a	n/a
8	CEBPB	chr1:76802794-76803000	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr1:76802670-76803012	ECC-1	luminal epithelium:	n/a	n/a
10	CEBPB	chr1:76831038-76831227	A549	lung:	n/a	chr1:76831106-76831117
11	CEBPB	chr1:76784987-76785293	HepG2	liver:	n/a	chr1:76785133-76785144
12	CEBPB	chr1:76784975-76785274	IMR90	lung:	n/a	chr1:76785133-76785144
13	CEBPB	chr1:76831025-76831218	HepG2	liver:	n/a	chr1:76831106-76831117
14	CEBPB	chr1:76891368-76891765	IMR90	lung:	n/a	n/a
15	CEBPB	chr1:76899228-76899474	IMR90	lung:	n/a	n/a
16	CEBPB	chr1:76892319-76892660	IMR90	lung:	n/a	n/a
17	CEBPB	chr1:76802693-76803049	IMR90	lung:	n/a	n/a
18	CEBPB	chr1:76796607-76797014	IMR90	lung:	n/a	n/a
19	CEBPB	chr1:76880910-76881074	HepG2	liver:	n/a	chr1:76880987-76880998
20	CEBPB	chr1:76802772-76802992	ECC-1	luminal epithelium:	n/a	n/a
21	CTCF	chr1:76796780-76796930	HCM	heart:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885 chr1:76796870-76796891
22	CTCF	chr1:76809558-76809729	LNCaP	prostate:	n/a	n/a
23	CTCF	chr1:76796727-76797029	MCF-7	breast:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885 chr1:76796870-76796891
24	CTCF	chr1:76796800-76796950	HUVEC	blood vessel:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885 chr1:76796870-76796891
25	CTCF	chr1:76796780-76796930	GM12873	blood:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885 chr1:76796870-76796891
26	CTCF	chr1:76796720-76796870	HRPEpiC	eye:	n/a	n/a
27	CTCF	chr1:76787223-76787315	Spleen_OC	spleen:	n/a	chr1:76787307-76787315
28	CTCF	chr1:76797280-76797430	GM12873	blood:	n/a	n/a
29	CTCF	chr1:76796800-76796950	SK-N-SH_RA	brain:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885 chr1:76796870-76796891
30	CTCF	chr1:76811680-76811830	HCT-116	colon:	n/a	n/a
31	CTCF	chr1:76796718-76797005	K562	blood:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885 chr1:76796870-76796891
32	CTCF	chr1:76796656-76797030	SK-N-SH_RA	brain:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885 chr1:76796870-76796891
33	CTCF	chr1:76796780-76796930	HCFaa	heart:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885 chr1:76796870-76796891
34	CTCF	chr1:76796820-76796970	HPAF	blood vessel:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885 chr1:76796870-76796891
35	CTCF	chr1:76796760-76796910	HEK293	kidney:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885 chr1:76796870-76796891
36	CTCF	chr1:76809600-76809750	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr1:76796800-76796950	GM12865	blood:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885 chr1:76796870-76796891
38	CTCF	chr1:76811620-76811770	HPAF	blood vessel:	n/a	n/a
39	CTCF	chr1:76787120-76787270	RPTEC	kidney:	n/a	n/a
40	CTCF	chr1:76796740-76796890	BE2_C	brain:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885
41	CTCF	chr1:76796720-76796870	NHLF	lung:	n/a	n/a
42	CTCF	chr1:76796739-76796956	Fibrobl	skin:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885 chr1:76796870-76796891
43	CTCF	chr1:76796555-76796615	GM10248	blood:	n/a	n/a
44	CTCF	chr1:76811660-76811810	AG04450	lung:	n/a	n/a
45	CTCF	chr1:76809569-76809671	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr1:76795911-76795988	GM20000	blood:	n/a	n/a
47	CTCF	chr1:76796763-76796943	GM12892	blood:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885 chr1:76796870-76796891
48	CTCF	chr1:76796800-76796950	HA-sp	spinal cord:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885 chr1:76796870-76796891
49	CTCF	chr1:76796760-76796910	GM12873	blood:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885 chr1:76796870-76796891
50	CTCF	chr1:76796820-76796970	SK-N-SH_RA	brain:	n/a	chr1:76796868-76796886 chr1:76796871-76796880 chr1:76796869-76796885 chr1:76796870-76796891

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:76817670-76817720	HAEpiC	amniotic membrane:	n/a
2	chr1:76780549-76780599	GM12892	blood:	n/a
3	chr1:76817670-76817720	HAEpiC	amniotic membrane:	n/a
4	chr1:76780549-76780599	GM12892	blood:	n/a
5	chr1:76840032-76840082	HEEpiC	esophagus:	n/a
6	chr1:76840032-76840082	NH-A	brain:	n/a
7	chr1:76817670-76817720	HIPEpiC	eye:	n/a
8	chr1:76891398-76891448	MCF10A-Er-Src	breast:	n/a
9	chr1:76899846-76899896	AG04450	lung:	fetal
10	chr1:76782984-76783034	HRE	kidney:	n/a
11	chr1:76782984-76783034	U87	brain:	n/a
12	chr1:76817670-76817720	SK-N-MC	brain:	n/a
13	chr1:76780549-76780599	GM12891	blood:	n/a
14	chr1:76817670-76817720	CMK	blood:	n/a
15	chr1:76782984-76783034	NHDF-neo	bronchial:	n/a
16	chr1:76899846-76899896	SK-N-MC	brain:	n/a
17	chr1:76782984-76783034	Hepatocyte	liver:	n/a
18	chr1:76780549-76780599	Hepatocyte	liver:	n/a
19	chr1:76780549-76780599	HL-60	blood:	n/a
20	chr1:76899846-76899896	AG09319	gingival:	n/a
21	chr1:76782984-76783034	PANC-1	pancreas:	n/a
22	chr1:76899846-76899896	PFSK-1	brain:	n/a
23	chr1:76840032-76840082	HRCEpiC	kidney:	n/a
24	chr1:76899846-76899896	Hela-S3	cervix:	n/a
25	chr1:76899846-76899896	HMEC	breast:	n/a
26	chr1:76891398-76891448	HCF	heart:	n/a
27	chr1:76817670-76817720	SAEC	small airway:	n/a
28	chr1:76840032-76840082	HIPEpiC	eye:	n/a
29	chr1:76840032-76840082	HCF	heart:	n/a
30	chr1:76782984-76783034	NT2-D1	testis:	n/a
31	chr1:76840032-76840082	PANC-1	pancreas:	n/a
32	chr1:76817670-76817720	AG10803	skin:	n/a
33	chr1:76899846-76899896	HepG2	liver:	n/a
34	chr1:76899846-76899896	AoSMC	blood vessel:	n/a
35	chr1:76817670-76817720	HCF	heart:	n/a
36	chr1:76840032-76840082	MCF10A-Er-Src	breast:	n/a
37	chr1:76891398-76891448	AG04450	lung:	fetal
38	chr1:76891398-76891448	PrEC	prostate:	n/a
39	chr1:76780549-76780599	NH-A	brain:	n/a
40	chr1:76899846-76899896	BJ	skin:	n/a
41	chr1:76817670-76817720	Jurkat	blood:	n/a
42	chr1:76782984-76783034	CMK	blood:	n/a
43	chr1:76899846-76899896	SKMC	muscle:	n/a
44	chr1:76782984-76783034	HNPCEpiC	eye:	n/a
45	chr1:76899846-76899896	K562	blood:	n/a
46	chr1:76891398-76891448	IMR90	lung:	fetal
47	chr1:76891398-76891448	ovcar-3	ovarian:	n/a
48	chr1:76891398-76891448	SK-N-SH_RA	brain:	n/a
49	chr1:76840032-76840082	LNCaP	prostate:	n/a
50	chr1:76891398-76891448	SK-N-SH	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:76885764..76887919-chr1:76891776..76893368,2	K562	blood:
2	chr1:76816508..76818358-chr1:76820395..76822942,2	K562	blood:
3	chr1:76782991..76784756-chr1:76794906..76796541,2	K562	blood:
4	chr1:76884483..76887341-chr1:76890524..76892236,2	MCF-7	breast:
5	chr1:76780616..76783208-chr1:76783667..76786559,2	K562	blood:
6	chr1:76796528..76797295-chr1:77206308..77207068,2	MCF-7	breast:
7	chr1:76880275..76881877-chr1:76884344..76886565,2	K562	blood:
8	chr1:76870428..76873153-chr1:76875050..76877438,2	K562	blood:
9	chr1:76796470..76797076-chr1:77591559..77592349,2	MCF-7	breast:
10	chr1:76796476..76797352-chr1:77609351..77609861,2	K562	blood:
11	chr1:76816508..76818358-chr1:76820395..76822942,2	K562	blood:
12	chr1:76870428..76873153-chr1:76875050..76877438,2	K562	blood:
13	chr1:76373718..76374271-chr1:76796370..76797302,2	MCF-7	breast:
14	chr1:76620098..76620620-chr1:76796654..76797328,2	MCF-7	breast:
15	chr1:76756888..76759692-chr1:76896597..76899350,2	K562	blood:
16	chr1:76884483..76887341-chr1:76890524..76892236,2	MCF-7	breast:
17	chr1:76782991..76784756-chr1:76794906..76796541,2	K562	blood:
18	chr1:76796389..76797022-chr1:77608917..77609894,2	MCF-7	breast:
19	chr1:76880275..76881877-chr1:76884344..76886565,2	K562	blood:
20	chr1:76796406..76797312-chr1:77366615..77367452,3	MCF-7	breast:
21	chr1:76885764..76887919-chr1:76891776..76893368,2	K562	blood:
22	chr1:76813366..76816327-chr1:76818310..76820003,2	K562	blood:
23	chr1:76871350..76874295-chr1:76994896..76997570,2	K562	blood:
24	chr1:76780616..76783208-chr1:76783667..76786559,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ASB17-2	chr1:76819268-76819931	NONHSAT004012

Variant related genes	Relation type
ST6GALNAC3	TF binding region
ENSG00000223905	TF binding region
ST6GALNAC3	CpG island
ENSG00000223905	CpG island
ENSG00000223905	chromatin interactions

Extended variants
information (count: 4040 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:4040 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543420737	chr1:76777385-76777386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs376980548	chr1:76777400-76777401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs138496748	chr1:76777418-76777419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs530599940	chr1:76777462-76777463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs541247859	chr1:76777486-76777487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs182770350	chr1:76777523-76777524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs533460361	chr1:76777572-76777573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs12137229	chr1:76777586-76777587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs563783336	chr1:76777594-76777595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs537585318	chr1:76777601-76777602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs187484530	chr1:76777660-76777661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs368365819	chr1:76777715-76777716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs146699247	chr1:76777821-76777822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs535775443	chr1:76777840-76777841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs139359604	chr1:76777848-76777849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs35370534	chr1:76777850-76777851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs397734350	chr1:76777857-76777858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs547180030	chr1:76777927-76777928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs9700636	chr1:76777928-76777929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs539253336	chr1:76777937-76777938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs557396197	chr1:76777956-76777957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs192374878	chr1:76778017-76778018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs141657969	chr1:76778033-76778034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs563052085	chr1:76778040-76778041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs574239709	chr1:76778068-76778069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs541755597	chr1:76778143-76778144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs183640844	chr1:76778183-76778184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs150522347	chr1:76778187-76778188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs376622160	chr1:76778209-76778210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs138377985	chr1:76778222-76778223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs373191806	chr1:76778261-76778262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs78754057	chr1:76778270-76778271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs531062411	chr1:76778277-76778278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs377258649	chr1:76778315-76778316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs187400448	chr1:76778322-76778323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs561377358	chr1:76778402-76778403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs369608664	chr1:76778434-76778435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs547244939	chr1:76778492-76778493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs565651437	chr1:76778496-76778497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs149334008	chr1:76778552-76778553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs551187218	chr1:76778571-76778572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs113701548	chr1:76778609-76778610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs116072014	chr1:76778636-76778637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs192046556	chr1:76778638-76778639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs555064110	chr1:76778639-76778640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs184102475	chr1:76778654-76778655	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs34793833	chr1:76778689-76778690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs534610484	chr1:76778703-76778704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs6685923	chr1:76778746-76778747	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs578255740	chr1:76778750-76778751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:529 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:76755800-76783000	Weak transcription	Fetal Lung	lung
2	chr1:76760400-76779200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr1:76774200-76796400	Weak transcription	Fetal Stomach	stomach
4	chr1:76775400-76796400	Weak transcription	Brain Substantia Nigra	brain
5	chr1:76776400-76779600	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr1:76777000-76777600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr1:76778000-76782000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr1:76778400-76780200	Enhancers	Fetal Heart	heart
9	chr1:76778400-76783400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr1:76779000-76780600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr1:76779200-76779800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr1:76779200-76779800	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr1:76779200-76780200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr1:76779200-76780600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr1:76779400-76779800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr1:76779400-76780000	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr1:76779400-76780600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr1:76779600-76779800	Enhancers	Brain Hippocampus Middle	brain
19	chr1:76779600-76780000	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
20	chr1:76779600-76780600	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr1:76779800-76780200	Weak transcription	Brain Hippocampus Middle	brain
22	chr1:76779800-76780600	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr1:76779800-76782800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr1:76779800-76784000	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr1:76780200-76780600	Flanking Active TSS	Fetal Heart	heart
26	chr1:76780200-76784000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr1:76780200-76813800	Weak transcription	Primary B cells from cord blood	blood
28	chr1:76780600-76781600	Enhancers	Fetal Heart	heart
29	chr1:76780600-76783000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr1:76780600-76784000	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr1:76780600-76817200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr1:76781600-76783400	Weak transcription	Fetal Heart	heart
33	chr1:76781800-76782200	ZNF genes & repeats	Fetal Kidney	kidney
34	chr1:76782200-76792800	Weak transcription	Fetal Kidney	kidney
35	chr1:76782800-76783600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr1:76783000-76783400	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr1:76783000-76783600	Enhancers	Fetal Lung	lung
38	chr1:76783400-76783600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr1:76783400-76783600	Enhancers	Fetal Heart	heart
40	chr1:76783400-76784200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr1:76783600-76784600	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr1:76783600-76792000	Weak transcription	Fetal Lung	lung
43	chr1:76783600-76802600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr1:76784000-76784800	Enhancers	H1 Cell Line	embryonic stem cell
45	chr1:76784000-76784800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr1:76784000-76784800	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr1:76784000-76784800	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr1:76784200-76788400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr1:76784800-76787200	Weak transcription	HUVEC	blood vessel
50	chr1:76786800-76787200	Enhancers	Fetal Thymus	thymus

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