Variant report

Variant	nsv461806
Chromosome Location	chr1:70494216-70566981
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:477)
CpG islands
(count:183)
Chromatin interactive
region (count:26)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:477 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:70507413-70508355	K562	blood:	n/a	n/a
2	ARID3A	chr1:70516058-70516168	K562	blood:	n/a	n/a
3	ARID3A	chr1:70500148-70500446	K562	blood:	n/a	n/a
4	ATF1	chr1:70531620-70531733	K562	blood:	n/a	n/a
5	ATF1	chr1:70508023-70508451	K562	blood:	n/a	n/a
6	ATF1	chr1:70542996-70543014	K562	blood:	n/a	n/a
7	ATF1	chr1:70522460-70522734	K562	blood:	n/a	n/a
8	ATF1	chr1:70507065-70507752	K562	blood:	n/a	n/a
9	ATF3	chr1:70507425-70507826	K562	blood:	n/a	n/a
10	BACH1	chr1:70550207-70550511	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr1:70507441-70507755	K562	blood:	n/a	n/a
12	BACH1	chr1:70550258-70550499	K562	blood:	n/a	n/a
13	BACH1	chr1:70499988-70500046	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr1:70499196-70499403	GM12878	blood:	n/a	n/a
15	BHLHE40	chr1:70505111-70505270	K562	blood:	n/a	n/a
16	BHLHE40	chr1:70500094-70500465	K562	blood:	n/a	n/a
17	CCNT2	chr1:70500072-70500392	K562	blood:	n/a	n/a
18	CCNT2	chr1:70509626-70509826	K562	blood:	n/a	n/a
19	CCNT2	chr1:70507380-70507801	K562	blood:	n/a	chr1:70507597-70507617
20	CCNT2	chr1:70562576-70562696	K562	blood:	n/a	n/a
21	CCNT2	chr1:70508029-70508393	K562	blood:	n/a	n/a
22	CEBPB	chr1:70499985-70500315	K562	blood:	n/a	n/a
23	CEBPB	chr1:70507371-70507757	K562	blood:	n/a	n/a
24	CEBPB	chr1:70503670-70503981	K562	blood:	n/a	n/a
25	CEBPB	chr1:70554183-70554206	K562	blood:	n/a	chr1:70554187-70554198
26	CEBPB	chr1:70542764-70543105	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr1:70550813-70551667	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr1:70503631-70503918	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr1:70554100-70554304	HepG2	liver:	n/a	chr1:70554187-70554198
30	CEBPB	chr1:70556599-70556981	Hela-S3	cervix:	n/a	chr1:70556791-70556802
31	CEBPB	chr1:70556597-70557013	IMR90	lung:	n/a	chr1:70556791-70556802
32	CEBPB	chr1:70553401-70553582	K562	blood:	n/a	chr1:70553532-70553543
33	CEBPB	chr1:70542757-70543092	K562	blood:	n/a	n/a
34	CEBPB	chr1:70556614-70556936	ECC-1	luminal epithelium:	n/a	chr1:70556791-70556802
35	CEBPB	chr1:70556617-70556902	ECC-1	luminal epithelium:	n/a	chr1:70556791-70556802
36	CEBPB	chr1:70556688-70556888	HepG2	liver:	n/a	chr1:70556791-70556802
37	CEBPB	chr1:70506897-70508155	K562	blood:	n/a	n/a
38	CEBPB	chr1:70503731-70503934	IMR90	lung:	n/a	n/a
39	CEBPB	chr1:70531843-70532108	HepG2	liver:	n/a	chr1:70531988-70531999
40	CEBPB	chr1:70545345-70545550	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr1:70509519-70509858	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr1:70519194-70519468	K562	blood:	n/a	n/a
43	CEBPB	chr1:70506879-70508308	K562	blood:	n/a	n/a
44	CEBPB	chr1:70553423-70553637	HepG2	liver:	n/a	chr1:70553532-70553543
45	CEBPD	chr1:70507324-70507868	K562	blood:	n/a	n/a
46	CHD2	chr1:70507795-70507995	K562	blood:	n/a	n/a
47	CTCF	chr1:70500260-70500410	HEEpiC	esophagus:	n/a	n/a
48	CTCF	chr1:70500120-70500270	WI-38	lung:	n/a	n/a
49	CTCF	chr1:70500240-70500390	AG04449	skin:	n/a	n/a
50	CTCF	chr1:70500200-70500350	AG10803	skin:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:70501250-70501300	MCF-7	breast:	n/a
2	chr1:70501250-70501300	HepG2	liver:	n/a
3	chr1:70501250-70501300	HL-60	blood:	n/a
4	chr1:70509936-70509986	BE2_C	brain:	n/a
5	chr1:70501250-70501300	SKMC	muscle:	n/a
6	chr1:70500419-70500469	SK-N-MC	brain:	n/a
7	chr1:70501250-70501300	AG09309	skin:	n/a
8	chr1:70509936-70509986	SAEC	small airway:	n/a
9	chr1:70501250-70501300	T-47D	breast:	n/a
10	chr1:70501250-70501300	NB4	blood:	n/a
11	chr1:70500419-70500469	HepG2	liver:	n/a
12	chr1:70501250-70501300	SAEC	small airway:	n/a
13	chr1:70501250-70501300	HEK293	kidney:	embryo
14	chr1:70500419-70500469	GM19239	blood:	n/a
15	chr1:70509936-70509986	GM12891	blood:	n/a
16	chr1:70501250-70501300	Hela-S3	cervix:	n/a
17	chr1:70501250-70501300	HIPEpiC	eye:	n/a
18	chr1:70501250-70501300	RPTEC	kidney:	n/a
19	chr1:70501250-70501300	K562	blood:	n/a
20	chr1:70509936-70509986	NB4	blood:	n/a
21	chr1:70509936-70509986	HIPEpiC	eye:	n/a
22	chr1:70500419-70500469	PFSK-1	brain:	n/a
23	chr1:70501250-70501300	IMR90	lung:	fetal
24	chr1:70509936-70509986	U87	brain:	n/a
25	chr1:70509936-70509986	MCF10A-Er-Src	breast:	n/a
26	chr1:70500419-70500469	PrEC	prostate:	n/a
27	chr1:70501250-70501300	GM19239	blood:	n/a
28	chr1:70509936-70509986	HEEpiC	esophagus:	n/a
29	chr1:70509936-70509986	NHDF-neo	bronchial:	n/a
30	chr1:70501250-70501300	HCF	heart:	n/a
31	chr1:70500419-70500469	AG09309	skin:	n/a
32	chr1:70501250-70501300	BE2_C	brain:	n/a
33	chr1:70501250-70501300	Hepatocyte	liver:	n/a
34	chr1:70500419-70500469	SK-N-SH_RA	brain:	n/a
35	chr1:70501250-70501300	AG10803	skin:	n/a
36	chr1:70509936-70509986	NT2-D1	testis:	n/a
37	chr1:70509936-70509986	HMEC	breast:	n/a
38	chr1:70500419-70500469	HIPEpiC	eye:	n/a
39	chr1:70501250-70501300	AG04450	lung:	fetal
40	chr1:70501250-70501300	NHDF-neo	bronchial:	n/a
41	chr1:70500419-70500469	HAEpiC	amniotic membrane:	n/a
42	chr1:70501250-70501300	MCF10A-Er-Src	breast:	n/a
43	chr1:70500419-70500469	GM12892	blood:	n/a
44	chr1:70501250-70501300	AG04449	skin:	fetal
45	chr1:70501250-70501300	LNCaP	prostate:	n/a
46	chr1:70509936-70509986	AG04450	lung:	fetal
47	chr1:70501250-70501300	PFSK-1	brain:	n/a
48	chr1:70500419-70500469	NHDF-neo	bronchial:	n/a
49	chr1:70509936-70509986	CMK	blood:	n/a
50	chr1:70500419-70500469	BE2_C	brain:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:70537552..70539411-chr1:70545771..70549953,3	K562	blood:
2	chr1:70504669..70508313-chr1:70509431..70511799,3	K562	blood:
3	chr1:70488967..70491122-chr1:70493902..70495892,2	K562	blood:
4	chr1:70552623..70554751-chr1:70557187..70559159,2	K562	blood:
5	chr1:70499352..70501847-chr1:70502427..70503999,2	K562	blood:
6	chr1:70495317..70498678-chr1:70499423..70502142,3	K562	blood:
7	chr1:70506553..70508330-chr1:70513862..70516733,2	K562	blood:
8	chr1:70512841..70514929-chr1:70517630..70519621,2	K562	blood:
9	chr1:70500217..70500734-chr1:70975931..70976504,2	K562	blood:
10	chr1:70499914..70500706-chr1:70608453..70608981,2	MCF-7	breast:
11	chr1:70522889..70525651-chr1:70527610..70529469,2	K562	blood:
12	chr1:70522889..70525651-chr1:70527610..70529469,2	K562	blood:
13	chr1:70497178..70499324-chr1:70500642..70503385,2	K562	blood:
14	chr1:70500723..70504696-chr1:70505322..70508157,4	K562	blood:
15	chr1:70497178..70499324-chr1:70500642..70503385,2	K562	blood:
16	chr1:70531477..70533272-chr1:70537582..70540486,2	K562	blood:
17	chr1:70499352..70501847-chr1:70502427..70503999,2	K562	blood:
18	chr1:70512841..70514929-chr1:70517630..70519621,2	K562	blood:
19	chr1:70506553..70508330-chr1:70513862..70516733,2	K562	blood:
20	chr1:70537552..70539411-chr1:70545771..70549953,3	K562	blood:
21	chr1:70504669..70508313-chr1:70509431..70511799,3	K562	blood:
22	chr1:70531477..70533272-chr1:70537582..70540486,2	K562	blood:
23	chr1:70552623..70554751-chr1:70557187..70559159,2	K562	blood:
24	chr1:70500723..70504696-chr1:70505322..70508157,4	K562	blood:
25	chr1:70489437..70491215-chr1:70493568..70495892,3	K562	blood:
26	chr1:70499830..70500350-chr1:70953253..70954208,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRC40-2	chr1:70496815-70496905	ENSG00000237919.1

No data

Variant related genes	Relation type
ENSG00000237919	TF binding region
ENSG00000237919	CpG island
ENSG00000237919	chromatin interactions

Extended variants
information (count: 2405 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:2405 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2291777	chr1:70494216-70494217	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs558491048	chr1:70494230-70494231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs572372639	chr1:70494247-70494248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs541470140	chr1:70494302-70494303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs561023694	chr1:70494324-70494325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs376204001	chr1:70494339-70494340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs574968217	chr1:70494340-70494341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs12039381	chr1:70494369-70494370	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs111571409	chr1:70494390-70494391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs575731891	chr1:70494412-70494413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs532890972	chr1:70494492-70494493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs532033525	chr1:70494519-70494520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs548860382	chr1:70494549-70494550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs559272553	chr1:70494600-70494601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs562270532	chr1:70494607-70494608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs149307961	chr1:70494611-70494612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs373632233	chr1:70494620-70494621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs192482503	chr1:70494637-70494638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs147403487	chr1:70494723-70494724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs530600659	chr1:70494746-70494747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs183960113	chr1:70494801-70494802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs61782626	chr1:70494825-70494826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs539321850	chr1:70494864-70494865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs10493464	chr1:70494915-70494916	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs138204637	chr1:70494927-70494928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs60482157	chr1:70494932-70494933	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs555045346	chr1:70494933-70494934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs574863673	chr1:70494950-70494951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs186693677	chr1:70494969-70494970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs192980374	chr1:70495014-70495015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs184607585	chr1:70495034-70495035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs11209585	chr1:70495045-70495046	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs190327253	chr1:70495062-70495063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs556706256	chr1:70495076-70495077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs559803783	chr1:70495090-70495091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs528077895	chr1:70495116-70495117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs541505539	chr1:70495129-70495130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs567336655	chr1:70495141-70495142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs561808376	chr1:70495166-70495167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs59882156	chr1:70495179-70495180	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs397707526	chr1:70495187-70495188	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs530491478	chr1:70495188-70495189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs60142527	chr1:70495234-70495235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs1327885	chr1:70495244-70495245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs536362223	chr1:70495247-70495248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs10493465	chr1:70495253-70495254	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs546865036	chr1:70495271-70495272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs566700109	chr1:70495294-70495295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs534995741	chr1:70495306-70495307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs181480753	chr1:70495308-70495309	Weak transcription Enhancers	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
small cell lung cancer	20016488	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
Esophageal cancer	21851588	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:297 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:70464800-70509000	Weak transcription	Brain Angular Gyrus	brain
2	chr1:70478000-70503800	Weak transcription	Brain Cingulate Gyrus	brain
3	chr1:70479400-70515600	Weak transcription	Fetal Brain Male	brain
4	chr1:70479800-70503800	Weak transcription	Fetal Muscle Trunk	muscle
5	chr1:70485200-70503800	Weak transcription	Brain Germinal Matrix	brain
6	chr1:70485600-70503800	Weak transcription	Brain Anterior Caudate	brain
7	chr1:70488000-70503200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr1:70488000-70503800	Weak transcription	Fetal Muscle Leg	muscle
9	chr1:70489400-70501400	Weak transcription	Fetal Brain Female	brain
10	chr1:70492800-70495800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr1:70495000-70495800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr1:70495000-70496800	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr1:70495800-70496000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr1:70495800-70496800	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr1:70496800-70499800	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr1:70499000-70499400	Enhancers	GM12878-XiMat	blood
17	chr1:70499200-70500600	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr1:70499800-70500400	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr1:70499800-70500400	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr1:70499800-70500600	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr1:70499800-70500800	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr1:70500000-70500600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr1:70500000-70501200	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr1:70500200-70500800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr1:70500200-70506200	Weak transcription	Brain Hippocampus Middle	brain
26	chr1:70500400-70500600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
27	chr1:70500600-70501000	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr1:70500600-70503800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr1:70500600-70503800	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr1:70500600-70503800	Weak transcription	Pancreas	Pancrea
31	chr1:70501000-70509400	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr1:70501400-70505400	Strong transcription	Fetal Brain Female	brain
33	chr1:70503200-70503800	Weak transcription	Fetal Stomach	stomach
34	chr1:70503200-70504600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr1:70503200-70505000	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
36	chr1:70503400-70504400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr1:70503600-70504000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr1:70503600-70504400	Enhancers	HMEC	breast
39	chr1:70503800-70504000	ZNF genes & repeats	Fetal Stomach	stomach
40	chr1:70503800-70504200	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr1:70503800-70504200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr1:70503800-70504200	ZNF genes & repeats	Pancreas	Pancrea
43	chr1:70503800-70504600	ZNF genes & repeats	Brain Cingulate Gyrus	brain
44	chr1:70503800-70504600	Strong transcription	Fetal Muscle Leg	muscle
45	chr1:70503800-70505000	Strong transcription	Brain Anterior Caudate	brain
46	chr1:70503800-70505000	Strong transcription	Brain Inferior Temporal Lobe	brain
47	chr1:70503800-70505400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr1:70503800-70505400	Strong transcription	Fetal Muscle Trunk	muscle
49	chr1:70503800-70506000	Strong transcription	Brain Germinal Matrix	brain
50	chr1:70504000-70504200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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