Variant report

Variant	nsv1010655
Chromosome Location	chr1:62427826-62447302
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	ATF3	chr1:62433476-62433726	K562	blood:	n/a	n/a
2	BACH1	chr1:62446282-62446790	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr1:62446381-62446560	K562	blood:	n/a	n/a
4	BHLHE40	chr1:62437864-62437982	K562	blood:	n/a	n/a
5	CEBPB	chr1:62432189-62432433	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr1:62440023-62440267	HepG2	liver:	n/a	n/a
7	CEBPB	chr1:62446313-62446586	K562	blood:	n/a	n/a
8	CEBPB	chr1:62446295-62446907	K562	blood:	n/a	chr1:62446734-62446745 chr1:62446733-62446746 chr1:62446733-62446746
9	CEBPB	chr1:62440045-62440224	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr1:62446324-62446874	H1-hESC	embryonic stem cell:	n/a	chr1:62446734-62446745 chr1:62446733-62446746 chr1:62446733-62446746
11	CEBPB	chr1:62440045-62440218	K562	blood:	n/a	n/a
12	CEBPB	chr1:62446355-62446912	IMR90	lung:	n/a	chr1:62446734-62446745 chr1:62446733-62446746 chr1:62446733-62446746
13	CEBPB	chr1:62446583-62446870	HepG2	liver:	n/a	chr1:62446734-62446745 chr1:62446733-62446746 chr1:62446733-62446746
14	CHD2	chr1:62446418-62446581	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr1:62446374-62446425	Fibrobl	skin:	n/a	n/a
16	CTCF	chr1:62440228-62440270	Kidney_OC	kidney:	n/a	n/a
17	CUX1	chr1:62433241-62433259	K562	blood:	n/a	n/a
18	E2F4	chr1:62446465-62446664	MCF10A-Er-Src	breast:	n/a	chr1:62446509-62446518
19	E2F4	chr1:62440236-62440368	MCF10A-Er-Src	breast:	n/a	n/a
20	E2F4	chr1:62438634-62439009	MCF10A-Er-Src	breast:	n/a	n/a
21	EP300	chr1:62433430-62433743	SK-N-SH_RA	brain:	n/a	chr1:62433649-62433657 chr1:62433655-62433664 chr1:62433702-62433716 chr1:62433479-62433493
22	EP300	chr1:62432611-62432792	K562	blood:	n/a	n/a
23	EP300	chr1:62433418-62433730	SK-N-SH_RA	brain:	n/a	chr1:62433649-62433657 chr1:62433655-62433664 chr1:62433702-62433716 chr1:62433479-62433493
24	ESR1	chr1:62432481-62432805	T-47D	breast:	n/a	n/a
25	ESR1	chr1:62432573-62432749	T-47D	breast:	n/a	n/a
26	FOS	chr1:62438813-62439128	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr1:62440032-62440239	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr1:62438769-62439219	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr1:62446306-62446560	MCF10A-Er-Src	breast:	n/a	chr1:62446463-62446475 chr1:62446464-62446474
30	FOS	chr1:62446342-62446638	MCF10A-Er-Src	breast:	n/a	chr1:62446463-62446475 chr1:62446464-62446474
31	FOS	chr1:62440039-62440275	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr1:62438816-62439128	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr1:62440055-62440275	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr1:62446306-62446593	MCF10A-Er-Src	breast:	n/a	chr1:62446463-62446475 chr1:62446464-62446474
35	FOS	chr1:62440074-62440275	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr1:62446297-62446593	MCF10A-Er-Src	breast:	n/a	chr1:62446463-62446475 chr1:62446464-62446474
37	FOXA1	chr1:62441344-62441639	T-47D	breast:	n/a	n/a
38	FOXA1	chr1:62441400-62441592	T-47D	breast:	n/a	n/a
39	FOXP2	chr1:62446307-62446517	SK-N-MC	brain:	n/a	n/a
40	GATA2	chr1:62445408-62445710	K562	blood:	n/a	n/a
41	GATA2	chr1:62433432-62433718	SH-SY5Y	brain:	n/a	n/a
42	GATA3	chr1:62433139-62433695	SH-SY5Y	brain:	n/a	chr1:62433143-62433150 chr1:62433141-62433150 chr1:62433143-62433150 chr1:62433141-62433151 chr1:62433143-62433150
43	GATA3	chr1:62433236-62433904	SK-N-SH	brain:	n/a	n/a
44	GATA3	chr1:62441311-62441758	T-47D	breast:	n/a	n/a
45	GATA3	chr1:62432959-62433967	SK-N-SH	brain:	n/a	chr1:62433143-62433150 chr1:62433141-62433150 chr1:62433143-62433150 chr1:62433136-62433157 chr1:62433138-62433154 chr1:62433141-62433151 chr1:62433143-62433150
46	GATA3	chr1:62441303-62441694	T-47D	breast:	n/a	n/a
47	JUND	chr1:62433358-62433932	SK-N-SH	brain:	n/a	chr1:62433503-62433512
48	JUND	chr1:62433370-62433855	SK-N-SH	brain:	n/a	chr1:62433503-62433512
49	KAP1	chr1:62439825-62440303	U2OS	brain:	n/a	n/a
50	KAP1	chr1:62444569-62445769	HEK293	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:62445916-62445966	AG09309	skin:	n/a
2	chr1:62445916-62445966	AG09309	skin:	n/a
3	chr1:62445916-62445966	HUVEC	blood vessel:	n/a
4	chr1:62445916-62445966	HIPEpiC	eye:	n/a
5	chr1:62445916-62445966	Jurkat	blood:	n/a
6	chr1:62445916-62445966	SK-N-SH	brain:	n/a
7	chr1:62445916-62445966	AG04449	skin:	fetal
8	chr1:62445916-62445966	HAEpiC	amniotic membrane:	n/a
9	chr1:62445916-62445966	IMR90	lung:	fetal
10	chr1:62445916-62445966	BE2_C	brain:	n/a
11	chr1:62445916-62445966	HCM	heart:	n/a
12	chr1:62445916-62445966	CMK	blood:	n/a
13	chr1:62445916-62445966	Hela-S3	cervix:	n/a
14	chr1:62445916-62445966	HCPEpiC	choroid plexus:	n/a
15	chr1:62445916-62445966	NH-A	brain:	n/a
16	chr1:62445916-62445966	HRE	kidney:	n/a
17	chr1:62445916-62445966	NHDF-neo	bronchial:	n/a
18	chr1:62445916-62445966	LNCaP	prostate:	n/a
19	chr1:62445916-62445966	A549	lung:	n/a
20	chr1:62445916-62445966	ProgFib	skin:	n/a
21	chr1:62445916-62445966	HMEC	breast:	n/a
22	chr1:62445916-62445966	AoSMC	blood vessel:	n/a
23	chr1:62445916-62445966	BJ	skin:	n/a
24	chr1:62445916-62445966	HRCEpiC	kidney:	n/a
25	chr1:62445916-62445966	HEK293	kidney:	embryo
26	chr1:62445916-62445966	SAEC	small airway:	n/a
27	chr1:62445916-62445966	T-47D	breast:	n/a
28	chr1:62445916-62445966	U87	brain:	n/a
29	chr1:62445916-62445966	PFSK-1	brain:	n/a
30	chr1:62445916-62445966	MCF-7	breast:	n/a
31	chr1:62445916-62445966	NB4	blood:	n/a
32	chr1:62445916-62445966	H1-hESC	embryonic stem cell:	embryo
33	chr1:62445916-62445966	ovcar-3	ovarian:	n/a
34	chr1:62445916-62445966	AG10803	skin:	n/a
35	chr1:62445916-62445966	GM19239	blood:	n/a
36	chr1:62445916-62445966	AG04450	lung:	fetal
37	chr1:62445916-62445966	HPAEpiC	pulmonary alveolar:	n/a
38	chr1:62445916-62445966	HL-60	blood:	n/a
39	chr1:62445916-62445966	SKMC	muscle:	n/a
40	chr1:62445916-62445966	HCF	heart:	n/a
41	chr1:62445916-62445966	HEEpiC	esophagus:	n/a
42	chr1:62445916-62445966	GM06990	blood:	n/a
43	chr1:62445916-62445966	HNPCEpiC	eye:	n/a
44	chr1:62445916-62445966	PrEC	prostate:	n/a
45	chr1:62445916-62445966	HRPEpiC	eye:	n/a
46	chr1:62445916-62445966	MCF10A-Er-Src	breast:	n/a
47	chr1:62445916-62445966	SK-N-SH_RA	brain:	n/a
48	chr1:62445916-62445966	NHBE	bronchial:	n/a
49	chr1:62445916-62445966	GM12878	blood:	n/a
50	chr1:62445916-62445966	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:62444307..62446951-chr1:62447722..62450460,2	K562	blood:

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

Extended variants
information (count: 712 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:712 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145578210	chr1:62427827-62427828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs368488848	chr1:62427833-62427834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs7512525	chr1:62427888-62427889	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs547698028	chr1:62427994-62427995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs186729344	chr1:62428036-62428037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs191494002	chr1:62428148-62428149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs376682419	chr1:62428182-62428183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs369397493	chr1:62428191-62428192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs148884978	chr1:62428203-62428204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs570128698	chr1:62428207-62428208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs183282767	chr1:62428228-62428229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs558970135	chr1:62428242-62428243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs143490236	chr1:62428329-62428330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs552606134	chr1:62428351-62428352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs2482887	chr1:62428416-62428417	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs187910038	chr1:62428443-62428444	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs116795512	chr1:62428444-62428445	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs572297358	chr1:62428469-62428470	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs542797426	chr1:62428501-62428502	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs554500178	chr1:62428549-62428550	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs576063833	chr1:62428587-62428588	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs543134153	chr1:62428613-62428614	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs141958006	chr1:62428687-62428688	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs528983868	chr1:62428720-62428721	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs78674052	chr1:62428728-62428729	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs34896171	chr1:62428732-62428733	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs560519712	chr1:62428749-62428750	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs530370689	chr1:62428750-62428751	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs369823286	chr1:62428803-62428804	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs148079788	chr1:62428804-62428805	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs369207793	chr1:62428805-62428806	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs193034271	chr1:62428832-62428833	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs76619725	chr1:62428846-62428847	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs4915601	chr1:62428912-62428913	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs185143142	chr1:62428921-62428922	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs535012699	chr1:62428931-62428932	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs79977507	chr1:62428978-62428979	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs565949088	chr1:62428993-62428994	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs536181850	chr1:62429007-62429008	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs554718159	chr1:62429026-62429027	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs149438190	chr1:62429034-62429035	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs375211426	chr1:62429036-62429037	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs9436216	chr1:62429086-62429087	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs543070979	chr1:62429126-62429127	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs558236187	chr1:62429129-62429130	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs576579423	chr1:62429141-62429142	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs534698394	chr1:62429157-62429158	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs138517657	chr1:62429165-62429166	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs559121570	chr1:62429176-62429177	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs190429187	chr1:62429178-62429179	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Breast cancer	16620391	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
CNS Malformation Syndrome	17530927	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Colorectal cancer	20459617	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:172 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:62350600-62428200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr1:62385000-62494200	Weak transcription	Aorta	Aorta
3	chr1:62406600-62430200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr1:62409000-62436800	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr1:62409200-62456000	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr1:62409200-62456800	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr1:62409200-62457000	Weak transcription	Fetal Intestine Large	intestine
8	chr1:62409200-62518600	Weak transcription	Pancreas	Pancrea
9	chr1:62409400-62429600	Weak transcription	Gastric	stomach
10	chr1:62409400-62458400	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr1:62417800-62431600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr1:62418000-62428800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr1:62418200-62446400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr1:62418400-62441400	Weak transcription	Fetal Kidney	kidney
15	chr1:62418600-62432400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr1:62418600-62432400	Weak transcription	NHEK	skin
17	chr1:62418800-62432800	Weak transcription	HMEC	breast
18	chr1:62419600-62445800	Weak transcription	Left Ventricle	heart
19	chr1:62420800-62429800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
20	chr1:62422800-62432600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr1:62423400-62431200	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr1:62423400-62433600	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr1:62423600-62433800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr1:62423800-62432800	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr1:62424000-62432000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr1:62424200-62436600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
27	chr1:62424200-62494200	Weak transcription	Esophagus	oesophagus
28	chr1:62424800-62438200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr1:62425000-62441400	Weak transcription	Stomach Mucosa	stomach
30	chr1:62426200-62428400	Weak transcription	Fetal Intestine Small	intestine
31	chr1:62427200-62432800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr1:62428400-62428600	Enhancers	Right Atrium	heart
33	chr1:62428400-62430600	Strong transcription	Fetal Intestine Small	intestine
34	chr1:62430200-62430600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr1:62430600-62435400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr1:62430600-62442200	Weak transcription	Fetal Intestine Small	intestine
37	chr1:62431200-62431400	Enhancers	H9 Cell Line	embryonic stem cell
38	chr1:62431600-62432200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr1:62432000-62433400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr1:62432000-62435600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
41	chr1:62432200-62439000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr1:62432400-62433600	Enhancers	NHEK	skin
43	chr1:62432400-62434000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr1:62432600-62432800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr1:62432800-62433200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr1:62432800-62433400	Enhancers	HMEC	breast
47	chr1:62432800-62433600	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr1:62432800-62433800	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr1:62432800-62433800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr1:62433000-62434000	Enhancers	NH-A	brain

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