Variant report

Variant	nsv10328
Chromosome Location	chr1:77243831-77293297
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	CEBPB	chr1:77248449-77248821	Hela-S3	cervix:	n/a	chr1:77248584-77248593 chr1:77248582-77248595 chr1:77248582-77248595 chr1:77248582-77248593 chr1:77248584-77248593 chr1:77248582-77248593 chr1:77248583-77248594 chr1:77248584-77248593 chr1:77248584-77248593 chr1:77248582-77248595
2	CEBPB	chr1:77256460-77256657	A549	lung:	n/a	n/a
3	CEBPB	chr1:77248403-77248809	HepG2	liver:	n/a	chr1:77248584-77248593 chr1:77248582-77248595 chr1:77248582-77248595 chr1:77248582-77248593 chr1:77248584-77248593 chr1:77248582-77248593 chr1:77248583-77248594 chr1:77248584-77248593 chr1:77248584-77248593 chr1:77248582-77248595
4	CEBPB	chr1:77248438-77248766	A549	lung:	n/a	chr1:77248584-77248593 chr1:77248582-77248595 chr1:77248582-77248595 chr1:77248582-77248593 chr1:77248584-77248593 chr1:77248582-77248593 chr1:77248583-77248594 chr1:77248584-77248593 chr1:77248584-77248593 chr1:77248582-77248595
5	CEBPB	chr1:77249976-77250146	A549	lung:	n/a	chr1:77250003-77250014 chr1:77250003-77250016
6	CEBPB	chr1:77248431-77248783	IMR90	lung:	n/a	chr1:77248584-77248593 chr1:77248582-77248595 chr1:77248582-77248595 chr1:77248582-77248593 chr1:77248584-77248593 chr1:77248582-77248593 chr1:77248583-77248594 chr1:77248584-77248593 chr1:77248584-77248593 chr1:77248582-77248595
7	CHD1	chr1:77287433-77287446	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr1:77257140-77257290	GM12869	blood:	n/a	n/a
9	CTCF	chr1:77263300-77263450	WERI-Rb-1	eye:	n/a	n/a
10	CTCF	chr1:77251256-77251289	GM13976	blood:	n/a	n/a
11	CTCF	chr1:77263258-77263437	Medullo	brain:	n/a	n/a
12	CTCF	chr1:77288453-77288539	GM20000	blood:	n/a	n/a
13	CTCF	chr1:77249200-77249350	GM12869	blood:	n/a	n/a
14	E2F4	chr1:77248453-77248759	MCF10A-Er-Src	breast:	n/a	n/a
15	E2F4	chr1:77291860-77292116	MCF10A-Er-Src	breast:	n/a	n/a
16	EP300	chr1:77251899-77252545	SK-N-SH_RA	brain:	n/a	chr1:77252175-77252184 chr1:77252044-77252052
17	EP300	chr1:77265472-77265699	SK-N-SH_RA	brain:	n/a	n/a
18	EP300	chr1:77291698-77292084	SK-N-SH_RA	brain:	n/a	n/a
19	EP300	chr1:77259256-77259531	SK-N-SH_RA	brain:	n/a	n/a
20	EP300	chr1:77267724-77268202	SK-N-SH_RA	brain:	n/a	n/a
21	EP300	chr1:77259152-77259753	SK-N-SH	brain:	n/a	chr1:77259700-77259710
22	EP300	chr1:77267779-77268107	SK-N-SH_RA	brain:	n/a	n/a
23	EP300	chr1:77251856-77252535	SK-N-SH_RA	brain:	n/a	chr1:77252175-77252184 chr1:77252044-77252052
24	EP300	chr1:77291569-77292273	SK-N-SH	brain:	n/a	n/a
25	EP300	chr1:77291683-77292101	SK-N-SH_RA	brain:	n/a	n/a
26	EP300	chr1:77267261-77268598	SK-N-SH	brain:	n/a	n/a
27	EP300	chr1:77265015-77267069	SK-N-SH	brain:	n/a	n/a
28	FOS	chr1:77252120-77252320	MCF10A-Er-Src	breast:	n/a	chr1:77252175-77252185 chr1:77252175-77252185 chr1:77252175-77252185 chr1:77252175-77252185 chr1:77252176-77252185
29	FOS	chr1:77291738-77292197	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr1:77264853-77265072	MCF10A-Er-Src	breast:	n/a	chr1:77264978-77264985 chr1:77264978-77264987 chr1:77264978-77264986 chr1:77264976-77264987 chr1:77264977-77264986
31	FOS	chr1:77289886-77290139	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr1:77248426-77248810	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr1:77289823-77290178	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr1:77250105-77250214	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr1:77264868-77265076	HUVEC	blood vessel:	n/a	chr1:77264978-77264985 chr1:77264978-77264987 chr1:77264978-77264986 chr1:77264976-77264987 chr1:77264977-77264986
36	FOS	chr1:77248426-77248876	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr1:77248426-77248902	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr1:77291771-77292185	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr1:77248499-77248807	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr1:77291700-77292595	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr1:77285746-77286000	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr1:77289808-77290194	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr1:77264831-77265045	MCF10A-Er-Src	breast:	n/a	chr1:77264978-77264985 chr1:77264978-77264987 chr1:77264978-77264986 chr1:77264976-77264987 chr1:77264977-77264986
44	FOS	chr1:77291710-77292437	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr1:77264936-77265021	MCF10A-Er-Src	breast:	n/a	chr1:77264978-77264985 chr1:77264978-77264987 chr1:77264978-77264986 chr1:77264976-77264987 chr1:77264977-77264986
46	FOS	chr1:77264936-77265025	MCF10A-Er-Src	breast:	n/a	chr1:77264978-77264985 chr1:77264978-77264987 chr1:77264978-77264986 chr1:77264976-77264987 chr1:77264977-77264986
47	FOSL2	chr1:77291760-77292192	SK-N-SH	brain:	n/a	n/a
48	FOSL2	chr1:77251941-77252411	SK-N-SH	brain:	n/a	chr1:77252175-77252185 chr1:77252175-77252185 chr1:77252175-77252185 chr1:77252175-77252185 chr1:77252176-77252185
49	FOSL2	chr1:77291691-77292271	SK-N-SH	brain:	n/a	n/a
50	FOSL2	chr1:77259173-77259714	SK-N-SH	brain:	n/a	chr1:77259498-77259507

No.	Distal block	Cell Line	Cell type
1	chr1:77268124..77270530-chr1:77274080..77275666,2	MCF-7	breast:
2	chr1:77268124..77270530-chr1:77274080..77275666,2	MCF-7	breast:
3	chr1:77169289..77170251-chr1:77243231..77243897,2	MCF-7	breast:
4	chr1:77263566..77264086-chr12:6643239..6643753,2	HCT-116	colon:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PIGK-2	chr1:77244675-77244952	XLOC_000873

Variant related genes	Relation type
ENSG00000237552	TF binding region
ENSG00000111640	chromatin interactions

Extended variants
information (count: 1333 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:1333 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149405576	chr1:77243870-77243871	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs536470724	chr1:77243875-77243876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs555211849	chr1:77243900-77243901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs144355856	chr1:77243954-77243955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs370359808	chr1:77243955-77243956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs78979864	chr1:77243966-77243967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs557172576	chr1:77244042-77244043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs144760959	chr1:77244077-77244078	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs115292155	chr1:77244105-77244106	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs576462900	chr1:77244146-77244147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs544271435	chr1:77244186-77244187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs562465397	chr1:77244263-77244264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs369494835	chr1:77244274-77244275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs541667218	chr1:77244296-77244297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs560439891	chr1:77244301-77244302	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs527583199	chr1:77244323-77244324	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs116724067	chr1:77244358-77244359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs117826565	chr1:77244397-77244398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs148643682	chr1:77244457-77244458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs551028242	chr1:77244475-77244476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs78610966	chr1:77244528-77244529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs536817015	chr1:77244535-77244536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs114493697	chr1:77244536-77244537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs182498678	chr1:77244551-77244552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs566762408	chr1:77244573-77244574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs534204220	chr1:77244634-77244635	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs185388038	chr1:77244669-77244670	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs576398418	chr1:77244746-77244747	Weak transcription Enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
29	rs559301507	chr1:77244781-77244782	Weak transcription Enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
30	rs556183423	chr1:77244787-77244788	Weak transcription Enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
31	rs142095931	chr1:77244794-77244795	Weak transcription Enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
32	rs150727496	chr1:77244807-77244808	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
33	rs12089286	chr1:77244826-77244827	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs139452240	chr1:77244847-77244848	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
35	rs546098906	chr1:77244884-77244885	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
36	rs376556839	chr1:77244885-77244886	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
37	rs532506294	chr1:77244918-77244919	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
38	rs190637253	chr1:77244919-77244920	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
39	rs562956712	chr1:77245055-77245056	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs530135867	chr1:77245075-77245076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs541912431	chr1:77245151-77245152	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs561994071	chr1:77245152-77245153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs548307734	chr1:77245197-77245198	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs566699135	chr1:77245198-77245199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs145897219	chr1:77245211-77245212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs368119682	chr1:77245212-77245213	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs534143018	chr1:77245220-77245221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs184194987	chr1:77245230-77245231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs531088976	chr1:77245296-77245297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs570819467	chr1:77245338-77245339	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
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
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:67 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:77243600-77244000	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr1:77243600-77244600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr1:77243600-77244800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr1:77243600-77246600	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr1:77243800-77245000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr1:77244600-77244800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr1:77244800-77245000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr1:77244800-77245400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr1:77245000-77245800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr1:77245000-77245800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr1:77245000-77245800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr1:77245400-77251200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr1:77245800-77246800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr1:77245800-77246800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr1:77246400-77247400	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr1:77246600-77247200	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr1:77246800-77247000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr1:77246800-77247000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr1:77246800-77247200	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr1:77247000-77250000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr1:77247200-77247400	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr1:77247400-77247600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr1:77247400-77247800	Enhancers	Fetal Brain Male	brain
24	chr1:77247800-77249000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr1:77249000-77249400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr1:77249000-77255800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr1:77249800-77250000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
28	chr1:77250000-77250200	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
29	chr1:77251200-77252600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr1:77251600-77252400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr1:77252000-77252400	Enhancers	Fetal Lung	lung
32	chr1:77252400-77254600	Weak transcription	Fetal Lung	lung
33	chr1:77254600-77255000	Enhancers	Fetal Lung	lung
34	chr1:77263200-77264400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr1:77263600-77264000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr1:77264000-77266800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr1:77265400-77265800	Enhancers	Fetal Lung	lung
38	chr1:77265600-77266000	Enhancers	Brain Germinal Matrix	brain
39	chr1:77266800-77268000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr1:77268000-77273000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr1:77273000-77273400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr1:77273000-77273600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr1:77273000-77274200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr1:77273200-77274200	Enhancers	NHDF-Ad	bronchial
45	chr1:77273400-77278400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr1:77278200-77278400	Enhancers	Spleen	Spleen
47	chr1:77278400-77279200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr1:77278400-77279400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr1:77278800-77279600	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr1:77279200-77280000	Enhancers	iPS-20b Cell Line	embryonic stem cell

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