Variant report

Variant	nsv997990
Chromosome Location	chr1:76086763-76121738
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:312)
CpG islands
(count:61)
Chromatin interactive
region (count:25)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:312 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:76105897-76106242	K562	blood:	n/a	n/a
2	ATF1	chr1:76105885-76106222	K562	blood:	n/a	n/a
3	ATF1	chr1:76109354-76109542	K562	blood:	n/a	n/a
4	ATF2	chr1:76095599-76095993	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr1:76105917-76106244	K562	blood:	n/a	n/a
6	BHLHE40	chr1:76098240-76098424	GM12878	blood:	n/a	n/a
7	BHLHE40	chr1:76105293-76105429	K562	blood:	n/a	n/a
8	BHLHE40	chr1:76107180-76107438	K562	blood:	n/a	n/a
9	CBX3	chr1:76112759-76113226	K562	blood:	n/a	n/a
10	CCNT2	chr1:76105959-76106219	K562	blood:	n/a	n/a
11	CEBPB	chr1:76103189-76103319	A549	lung:	n/a	n/a
12	CEBPB	chr1:76097115-76097389	K562	blood:	n/a	chr1:76097287-76097298
13	CEBPB	chr1:76097153-76097386	MCF-7	breast:	n/a	chr1:76097287-76097298
14	CEBPB	chr1:76107129-76107469	K562	blood:	n/a	n/a
15	CEBPB	chr1:76097144-76097360	IMR90	lung:	n/a	chr1:76097287-76097298
16	CEBPB	chr1:76097115-76097483	HepG2	liver:	n/a	chr1:76097287-76097298
17	CEBPB	chr1:76107117-76107372	K562	blood:	n/a	n/a
18	CEBPB	chr1:76105433-76105469	K562	blood:	n/a	n/a
19	CEBPB	chr1:76103067-76103358	K562	blood:	n/a	n/a
20	CEBPB	chr1:76097234-76097355	HepG2	liver:	n/a	chr1:76097287-76097298
21	CHD2	chr1:76105240-76105351	K562	blood:	n/a	n/a
22	CTCF	chr1:76098140-76098290	AG09319	gingival:	n/a	n/a
23	CTCF	chr1:76098120-76098270	GM12871	blood:	n/a	n/a
24	CTCF	chr1:76106018-76106047	NHEK	skin:	n/a	n/a
25	CTCF	chr1:76098110-76098305	Lung_OC	lung:	n/a	n/a
26	CTCF	chr1:76098180-76098330	AG09319	gingival:	n/a	n/a
27	CTCF	chr1:76098120-76098270	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr1:76098097-76098358	GM12878	blood:	n/a	n/a
29	CTCF	chr1:76098120-76098270	GM12867	blood:	n/a	n/a
30	CTCF	chr1:76098120-76098270	HMF	breast:	n/a	n/a
31	CTCF	chr1:76095788-76095968	GM12878	blood:	n/a	n/a
32	CTCF	chr1:76098140-76098290	GM12869	blood:	n/a	n/a
33	CTCF	chr1:76098140-76098290	HCPEpiC	choroid plexus:	n/a	n/a
34	CTCF	chr1:76098220-76098370	WI-38	lung:	n/a	n/a
35	CTCF	chr1:76098140-76098290	GM12872	blood:	n/a	n/a
36	CTCF	chr1:76098140-76098290	GM12866	blood:	n/a	n/a
37	CTCF	chr1:76098088-76098350	A549	lung:	n/a	n/a
38	CTCF	chr1:76098155-76098259	Fibrobl	skin:	n/a	n/a
39	CTCF	chr1:76098146-76098300	GM20000	blood:	n/a	n/a
40	CTCF	chr1:76098122-76098350	GM10248	blood:	n/a	n/a
41	CTCF	chr1:76098220-76098370	GM12872	blood:	n/a	n/a
42	CTCF	chr1:76098140-76098290	HCT-116	colon:	n/a	n/a
43	CTCF	chr1:76098106-76098346	MCF-7	breast:	n/a	n/a
44	CTCF	chr1:76098160-76098310	GM12865	blood:	n/a	n/a
45	CTCF	chr1:76098340-76098490	NB4	blood:	n/a	n/a
46	CTCF	chr1:76098140-76098290	GM12870	blood:	n/a	n/a
47	CTCF	chr1:76105953-76106067	GM12891	blood:	n/a	n/a
48	CTCF	chr1:76097991-76098474	HCT-116	colon:	n/a	n/a
49	CTCF	chr1:76098120-76098270	BJ	skin:	n/a	n/a
50	CTCF	chr1:76098140-76098290	AG04450	lung:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:76095838-76095888	SK-N-SH	brain:	n/a
2	chr1:76095838-76095888	GM12891	blood:	n/a
3	chr1:76095838-76095888	K562	blood:	n/a
4	chr1:76095838-76095888	AoSMC	blood vessel:	n/a
5	chr1:76095838-76095888	HMEC	breast:	n/a
6	chr1:76095838-76095888	SAEC	small airway:	n/a
7	chr1:76095838-76095888	Hela-S3	cervix:	n/a
8	chr1:76095838-76095888	SK-N-SH_RA	brain:	n/a
9	chr1:76095838-76095888	HPAEpiC	pulmonary alveolar:	n/a
10	chr1:76095838-76095888	GM19239	blood:	n/a
11	chr1:76095838-76095888	HNPCEpiC	eye:	n/a
12	chr1:76095838-76095888	NT2-D1	testis:	n/a
13	chr1:76095838-76095888	RPTEC	kidney:	n/a
14	chr1:76095838-76095888	HepG2	liver:	n/a
15	chr1:76095838-76095888	BE2_C	brain:	n/a
16	chr1:76095838-76095888	HRPEpiC	eye:	n/a
17	chr1:76095838-76095888	HRE	kidney:	n/a
18	chr1:76095838-76095888	ProgFib	skin:	n/a
19	chr1:76095838-76095888	CMK	blood:	n/a
20	chr1:76095838-76095888	PFSK-1	brain:	n/a
21	chr1:76095838-76095888	A549	lung:	n/a
22	chr1:76095838-76095888	AG09309	skin:	n/a
23	chr1:76095838-76095888	GM06990	blood:	n/a
24	chr1:76095838-76095888	HRCEpiC	kidney:	n/a
25	chr1:76095838-76095888	MCF-7	breast:	n/a
26	chr1:76095838-76095888	BJ	skin:	n/a
27	chr1:76095838-76095888	AG09319	gingival:	n/a
28	chr1:76095838-76095888	U87	brain:	n/a
29	chr1:76095838-76095888	NH-A	brain:	n/a
30	chr1:76095838-76095888	HIPEpiC	eye:	n/a
31	chr1:76095838-76095888	HL-60	blood:	n/a
32	chr1:76095838-76095888	IMR90	lung:	fetal
33	chr1:76095838-76095888	NHDF-neo	bronchial:	n/a
34	chr1:76095838-76095888	HCF	heart:	n/a
35	chr1:76095838-76095888	Hepatocyte	liver:	n/a
36	chr1:76095838-76095888	AG10803	skin:	n/a
37	chr1:76095838-76095888	MCF10A-Er-Src	breast:	n/a
38	chr1:76095838-76095888	NB4	blood:	n/a
39	chr1:76095838-76095888	LNCaP	prostate:	n/a
40	chr1:76095838-76095888	HCM	heart:	n/a
41	chr1:76095838-76095888	T-47D	breast:	n/a
42	chr1:76095838-76095888	PrEC	prostate:	n/a
43	chr1:76095838-76095888	AG04450	lung:	fetal
44	chr1:76095838-76095888	AG04449	skin:	fetal
45	chr1:76095838-76095888	H1-hESC	embryonic stem cell:	embryo
46	chr1:76095838-76095888	HEK293	kidney:	embryo
47	chr1:76095838-76095888	HCPEpiC	choroid plexus:	n/a
48	chr1:76095838-76095888	Jurkat	blood:	n/a
49	chr1:76095838-76095888	HUVEC	blood vessel:	n/a
50	chr1:76095838-76095888	ECC-1	luminal epithelium:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:76087110..76089218-chr1:76095459..76097902,2	MCF-7	breast:
2	chr1:76102793..76106233-chr1:76108594..76111145,3	K562	blood:
3	chr1:76103722..76106233-chr1:76108885..76111145,2	K562	blood:
4	chr1:76098237..76098781-chr1:76108716..76109281,2	K562	blood:
5	chr1:76094932..76097642-chr1:76105459..76107452,2	K562	blood:
6	chr1:76105051..76106564-chr1:76262176..76264540,2	K562	blood:
7	chr1:76081802..76083861-chr1:76085137..76086923,2	K562	blood:
8	chr1:76096029..76098574-chr1:76101114..76103972,2	K562	blood:
9	chr1:76116317..76118957-chr1:76120302..76123457,3	K562	blood:
10	chr1:76087110..76089218-chr1:76095459..76097902,2	MCF-7	breast:
11	chr1:76096029..76098574-chr1:76101114..76103972,2	K562	blood:
12	chr1:76080604..76083289-chr1:76094142..76096069,2	K562	blood:
13	chr1:76116317..76118957-chr1:76120302..76123457,3	K562	blood:
14	chr1:75698929..75699675-chr1:76097798..76098711,3	K562	blood:
15	chr1:76079931..76081989-chr1:76083963..76086787,2	K562	blood:
16	chr1:76097324..76099781-chr1:76183811..76186655,2	K562	blood:
17	chr1:75731173..75731698-chr1:76097693..76098339,2	MCF-7	breast:
18	chr1:76102793..76106233-chr1:76108594..76111145,3	K562	blood:
19	chr1:76094932..76097642-chr1:76105459..76107452,2	K562	blood:
20	chr1:76094259..76097858-chr1:76188776..76191867,4	K562	blood:
21	chr1:76088182..76090967-chr1:76093940..76095559,2	K562	blood:
22	chr1:76088182..76090967-chr1:76093940..76095559,2	K562	blood:
23	chr1:76083373..76085148-chr1:76086743..76089714,2	MCF-7	breast:
24	chr1:76103722..76106233-chr1:76108885..76111145,2	K562	blood:
25	chr1:76098237..76098781-chr1:76108716..76109281,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC44A5-4	chr1:76107988-76108177	NONHSAT003985
2	lnc-SLC44A5-4	chr1:76105925-76108177	NONHSAT003984
3	lnc-SLC44A5-4	chr1:76103852-76104725	NONHSAT003984

No data

Variant related genes	Relation type
ENSG00000230863	TF binding region
ENSG00000230863	CpG island
ENSG00000057468	chromatin interactions
ENSG00000178193	chromatin interactions
ENSG00000117054	chromatin interactions

Extended variants
information (count: 483 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:483 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532061890	chr1:76091287-76091288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs550194120	chr1:76091338-76091339	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs7553738	chr1:76091356-76091357	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs535479508	chr1:76091377-76091378	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs138023833	chr1:76091392-76091393	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs566138566	chr1:76091394-76091395	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs529763965	chr1:76091417-76091418	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs7553832	chr1:76091427-76091428	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs9787077	chr1:76091429-76091430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs558756992	chr1:76091433-76091434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs577089660	chr1:76091583-76091584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs77703901	chr1:76091634-76091635	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs187739458	chr1:76091635-76091636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs574419417	chr1:76091645-76091646	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs532357197	chr1:76091663-76091664	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs552492105	chr1:76091671-76091672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs34413559	chr1:76091691-76091692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs541411573	chr1:76091696-76091697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs9324206	chr1:76091734-76091735	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs4141467	chr1:76091842-76091843	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs545473140	chr1:76091859-76091860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs9324207	chr1:76091872-76091873	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs4141464	chr1:76091876-76091877	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs192906266	chr1:76091877-76091878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs545953893	chr1:76091898-76091899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs372773135	chr1:76091914-76091915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs529297985	chr1:76091928-76091929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs537523084	chr1:76091955-76091956	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs111388143	chr1:76091966-76091967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs556542029	chr1:76091979-76091980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs142902037	chr1:76092059-76092060	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs566199739	chr1:76092144-76092145	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs185111487	chr1:76092145-76092146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs1332783	chr1:76092166-76092167	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs17097106	chr1:76092180-76092181	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs537638634	chr1:76092183-76092184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs4949870	chr1:76092192-76092193	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs568222044	chr1:76092206-76092207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs535094452	chr1:76092322-76092323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs542177960	chr1:76092354-76092355	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs1332782	chr1:76092383-76092384	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs74372708	chr1:76092394-76092395	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs146079002	chr1:76092412-76092413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs140025140	chr1:76092448-76092449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs557430724	chr1:76092456-76092457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs576583348	chr1:76092461-76092462	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs543612958	chr1:76092483-76092484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs574355186	chr1:76092523-76092524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs562421785	chr1:76092571-76092572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs529533749	chr1:76092599-76092600	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:110)

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
abnormal development	18461090	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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:76091200-76092200	Enhancers	Dnd41	blood
2	chr1:76091800-76092800	Enhancers	HUVEC	blood vessel
3	chr1:76092400-76095800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr1:76094400-76094800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
5	chr1:76094600-76094800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
6	chr1:76094600-76095000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr1:76094600-76095400	Enhancers	HepG2	liver
8	chr1:76094600-76096200	Enhancers	H1 Cell Line	embryonic stem cell
9	chr1:76094600-76096800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr1:76094800-76096200	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr1:76094800-76096200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr1:76094800-76096800	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr1:76095000-76095200	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr1:76095000-76095200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr1:76095000-76096200	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr1:76095000-76096600	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr1:76095200-76095400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr1:76095200-76096200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr1:76095200-76096200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr1:76095200-76096200	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr1:76095200-76096200	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr1:76095400-76095600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr1:76095400-76096200	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr1:76095400-76096600	Weak transcription	HepG2	liver
25	chr1:76095400-76096800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr1:76095600-76096200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr1:76095800-76096200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr1:76095800-76096200	Enhancers	H9 Cell Line	embryonic stem cell
29	chr1:76095800-76096200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr1:76095800-76096200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr1:76096200-76098600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr1:76096400-76097600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
33	chr1:76096600-76097200	Enhancers	HepG2	liver
34	chr1:76098600-76098800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr1:76104400-76104800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr1:76104800-76105200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr1:76105200-76106200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr1:76105200-76106200	Enhancers	Pancreas	Pancrea
39	chr1:76105200-76106400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr1:76105200-76106400	Enhancers	K562	blood
41	chr1:76105200-76106600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr1:76105800-76106200	Enhancers	Esophagus	oesophagus
43	chr1:76108000-76108200	Enhancers	Esophagus	oesophagus
44	chr1:76109200-76109800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr1:76121000-76121400	ZNF genes & repeats	Aorta	Aorta

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