Variant report

Variant	nsv949472
Chromosome Location	chr2:35709203-36447481
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1785)
CpG islands
(count:307)
Chromatin interactive
region (count:35)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1785 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:36392370-36392619	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:36214717-36214956	HepG2	liver:	n/a	n/a
3	ATF2	chr2:36374728-36375202	GM12878	blood:	n/a	n/a
4	BACH1	chr2:36417402-36417520	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr2:36180017-36180019	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr2:36246312-36246349	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr2:36163349-36163414	K562	blood:	n/a	n/a
8	BATF	chr2:36374889-36375165	GM12878	blood:	n/a	n/a
9	BATF	chr2:36374886-36375226	GM12878	blood:	n/a	n/a
10	BCL11A	chr2:36374942-36375184	GM12878	blood:	n/a	chr2:36374970-36374979
11	BHLHE40	chr2:36411001-36411307	HepG2	liver:	n/a	n/a
12	BHLHE40	chr2:36115733-36115738	GM12878	blood:	n/a	n/a
13	BHLHE40	chr2:36214674-36215098	HepG2	liver:	n/a	n/a
14	BRCA1	chr2:36285622-36285667	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr2:36214839-36214902	HepG2	liver:	n/a	n/a
16	CCNT2	chr2:36229329-36229487	K562	blood:	n/a	n/a
17	CEBPB	chr2:36195265-36195307	K562	blood:	n/a	chr2:36195276-36195287
18	CEBPB	chr2:35721097-35721423	HepG2	liver:	n/a	chr2:35721266-35721283
19	CEBPB	chr2:35939874-35940327	HepG2	liver:	n/a	n/a
20	CEBPB	chr2:35966667-35966899	IMR90	lung:	n/a	n/a
21	CEBPB	chr2:36195210-36195394	IMR90	lung:	n/a	chr2:36195276-36195287
22	CEBPB	chr2:36108892-36109092	Hela-S3	cervix:	n/a	chr2:36108992-36109003
23	CEBPB	chr2:35748850-35749215	HepG2	liver:	n/a	chr2:35749027-35749038
24	CEBPB	chr2:36214584-36214999	H1-hESC	embryonic stem cell:	n/a	chr2:36214741-36214754 chr2:36214741-36214754 chr2:36214741-36214752
25	CEBPB	chr2:36379331-36379617	A549	lung:	n/a	chr2:36379457-36379468
26	CEBPB	chr2:36355084-36355143	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr2:35939980-35940327	K562	blood:	n/a	n/a
28	CEBPB	chr2:36214715-36214817	A549	lung:	n/a	chr2:36214741-36214754 chr2:36214741-36214754 chr2:36214741-36214752
29	CEBPB	chr2:36106593-36106880	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr2:36420124-36420491	ECC-1	luminal epithelium:	n/a	chr2:36420312-36420325
31	CEBPB	chr2:36305807-36305895	HepG2	liver:	n/a	chr2:36305858-36305869
32	CEBPB	chr2:36012772-36012798	HepG2	liver:	n/a	n/a
33	CEBPB	chr2:36420172-36420519	ECC-1	luminal epithelium:	n/a	chr2:36420312-36420325
34	CEBPB	chr2:36000765-36000949	A549	lung:	n/a	chr2:36000859-36000870 chr2:36000860-36000871
35	CEBPB	chr2:35931148-35931461	HepG2	liver:	n/a	chr2:35931306-35931319 chr2:35931306-35931317
36	CEBPB	chr2:35720194-35720493	MCF-7	breast:	n/a	n/a
37	CEBPB	chr2:36214535-36214977	HepG2	liver:	n/a	chr2:36214741-36214754 chr2:36214741-36214754 chr2:36214741-36214752
38	CEBPB	chr2:36436903-36436987	HepG2	liver:	n/a	n/a
39	CEBPB	chr2:36214566-36214940	HepG2	liver:	n/a	chr2:36214741-36214754 chr2:36214741-36214754 chr2:36214741-36214752
40	CEBPB	chr2:35735382-35735623	HepG2	liver:	n/a	n/a
41	CEBPB	chr2:35858453-35858678	HepG2	liver:	n/a	chr2:35858500-35858513 chr2:35858550-35858561 chr2:35858501-35858512
42	CEBPB	chr2:35719522-35719843	Hela-S3	cervix:	n/a	chr2:35719704-35719715 chr2:35719702-35719715 chr2:35719702-35719715
43	CEBPB	chr2:35734480-35734730	A549	lung:	n/a	chr2:35734589-35734600
44	CEBPB	chr2:35721104-35721408	A549	lung:	n/a	chr2:35721266-35721283
45	CEBPB	chr2:35725780-35725965	HepG2	liver:	n/a	chr2:35725883-35725894
46	CEBPB	chr2:35931181-35931345	H1-hESC	embryonic stem cell:	n/a	chr2:35931306-35931319 chr2:35931306-35931317
47	CEBPB	chr2:36044031-36044069	HepG2	liver:	n/a	chr2:36044042-36044055 chr2:36044042-36044055
48	CEBPB	chr2:36158170-36158415	IMR90	lung:	n/a	n/a
49	CEBPB	chr2:36195167-36195440	HepG2	liver:	n/a	chr2:36195276-36195287
50	CEBPB	chr2:36214637-36214840	HepG2	liver:	n/a	chr2:36214741-36214754 chr2:36214741-36214754 chr2:36214741-36214752

(count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:36018275-36018325	NB4	blood:	n/a
2	chr2:36157995-36158045	MCF10A-Er-Src	breast:	n/a
3	chr2:36018275-36018325	NB4	blood:	n/a
4	chr2:36157995-36158045	MCF10A-Er-Src	breast:	n/a
5	chr2:36049853-36049903	HRCEpiC	kidney:	n/a
6	chr2:36018275-36018325	H1-hESC	embryonic stem cell:	embryo
7	chr2:36018275-36018325	MCF10A-Er-Src	breast:	n/a
8	chr2:36018275-36018325	HEEpiC	esophagus:	n/a
9	chr2:36406592-36406642	PrEC	prostate:	n/a
10	chr2:36406592-36406642	Caco-2	colon:	n/a
11	chr2:36441749-36441799	Hela-S3	cervix:	n/a
12	chr2:36018275-36018325	A549	lung:	n/a
13	chr2:36406592-36406642	T-47D	breast:	n/a
14	chr2:36406592-36406642	AG04450	lung:	fetal
15	chr2:36018275-36018325	NHBE	bronchial:	n/a
16	chr2:36049853-36049903	SK-N-MC	brain:	n/a
17	chr2:36157995-36158045	AG04450	lung:	fetal
18	chr2:36441749-36441799	SAEC	small airway:	n/a
19	chr2:36049853-36049903	Hela-S3	cervix:	n/a
20	chr2:36441749-36441799	SK-N-SH	brain:	n/a
21	chr2:36157995-36158045	H1-hESC	embryonic stem cell:	embryo
22	chr2:36049853-36049903	U87	brain:	n/a
23	chr2:36018275-36018325	Caco-2	colon:	n/a
24	chr2:36049853-36049903	AG04450	lung:	fetal
25	chr2:36157995-36158045	K562	blood:	n/a
26	chr2:36406592-36406642	SAEC	small airway:	n/a
27	chr2:36018275-36018325	HCF	heart:	n/a
28	chr2:36406592-36406642	HCPEpiC	choroid plexus:	n/a
29	chr2:36441749-36441799	AG10803	skin:	n/a
30	chr2:36018275-36018325	HNPCEpiC	eye:	n/a
31	chr2:36157995-36158045	HAEpiC	amniotic membrane:	n/a
32	chr2:36441749-36441799	SK-N-MC	brain:	n/a
33	chr2:36441749-36441799	Hepatocyte	liver:	n/a
34	chr2:36157995-36158045	GM12891	blood:	n/a
35	chr2:36049853-36049903	ECC-1	luminal epithelium:	n/a
36	chr2:36406592-36406642	HRPEpiC	eye:	n/a
37	chr2:36441749-36441799	IMR90	lung:	fetal
38	chr2:36049853-36049903	T-47D	breast:	n/a
39	chr2:36406592-36406642	Hela-S3	cervix:	n/a
40	chr2:36441749-36441799	H1-hESC	embryonic stem cell:	embryo
41	chr2:36441749-36441799	GM06990	blood:	n/a
42	chr2:36157995-36158045	GM12892	blood:	n/a
43	chr2:36157995-36158045	AG09309	skin:	n/a
44	chr2:36441749-36441799	HRPEpiC	eye:	n/a
45	chr2:36157995-36158045	SK-N-MC	brain:	n/a
46	chr2:36157995-36158045	Jurkat	blood:	n/a
47	chr2:36441749-36441799	PFSK-1	brain:	n/a
48	chr2:36406592-36406642	SK-N-SH_RA	brain:	n/a
49	chr2:36049853-36049903	HEEpiC	esophagus:	n/a
50	chr2:36406592-36406642	CMK	blood:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:36262623..36264860-chr2:36265182..36267594,2	K562	blood:
2	chr14:33621149..33624012-chr2:35726795..35729641,2	MCF-7	breast:
3	chr2:36346980..36349018-chr2:36352266..36354440,2	K562	blood:
4	chr2:36167966..36170859-chr2:36172337..36174849,2	MCF-7	breast:
5	chr2:35847208..35849274-chr2:35852737..35854636,2	K562	blood:
6	chr2:35847208..35849274-chr2:35852737..35854636,2	K562	blood:
7	chr2:35863760..35866047-chr2:35869717..35871925,2	MCF-7	breast:
8	chr2:35887668..35890004-chr2:35892119..35894663,2	K562	blood:
9	chr2:35877173..35880679-chr2:35885712..35889508,3	MCF-7	breast:
10	chr2:35949877..35953265-chr2:35954228..35956588,3	MCF-7	breast:
11	chr2:35887668..35890004-chr2:35892119..35894663,2	K562	blood:
12	chr2:36375898..36378508-chr2:36382841..36384658,2	K562	blood:
13	chr2:36026668..36029472-chr2:36034547..36037398,2	K562	blood:
14	chr2:36243496..36245168-chr2:36248339..36251225,2	K562	blood:
15	chr2:35721064..35722615-chr2:35725696..35727810,2	MCF-7	breast:
16	chr2:36026668..36029472-chr2:36034547..36037398,2	K562	blood:
17	chr2:36198095..36199022-chr2:36584804..36585700,2	MCF-7	breast:
18	chr2:35863760..35866047-chr2:35869717..35871925,2	MCF-7	breast:
19	chr2:36208827..36211193-chr2:36213089..36216018,2	MCF-7	breast:
20	chr2:36426823..36429485-chr2:36432838..36434351,2	MCF-7	breast:
21	chr2:36426823..36429485-chr2:36432838..36434351,2	MCF-7	breast:
22	chr2:36243496..36245168-chr2:36248339..36251225,2	K562	blood:
23	chr2:36208827..36211193-chr2:36213089..36216018,2	MCF-7	breast:
24	chr2:36346980..36349018-chr2:36352266..36354440,2	K562	blood:
25	chr2:35878984..35880554-chr2:35880811..35883619,2	K562	blood:
26	chr2:36099243..36100067-chr2:36734209..36735134,2	MCF-7	breast:
27	chr2:35721064..35722615-chr2:35725696..35727810,2	MCF-7	breast:
28	chr2:35694136..35697118-chr2:35710618..35713142,3	MCF-7	breast:
29	chr2:36222475..36223224-chr6:31509383..31509944,2	MCF-7	breast:
30	chr2:36167966..36170859-chr2:36172337..36174849,2	MCF-7	breast:
31	chr2:35877173..35880679-chr2:35885712..35889508,3	MCF-7	breast:
32	chr2:36375898..36378508-chr2:36382841..36384658,2	K562	blood:
33	chr2:35878984..35880554-chr2:35880811..35883619,2	K562	blood:
34	chr2:36198079..36198752-chr2:36549195..36549978,3	MCF-7	breast:
35	chr2:36262623..36264860-chr2:36265182..36267594,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC007401.2.1-6	chr2:35949825-35950208	NONHSAT070075

No data

Variant related genes	Relation type
MRPL50P1	TF binding region
MRPL50P1	CpG island
ENSG00000229013	chromatin interactions
ENSG00000265301	chromatin interactions
ENSG00000207255	chromatin interactions
ENSG00000234587	chromatin interactions
ENSG00000198563	chromatin interactions

Extended variants
information (count: 17808 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:17808 , 50 per page) page: 1 2 3 4 5 6 7 ... 357

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539879976	chr2:35710623-35710624	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs538037021	chr2:35710632-35710633	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs185904791	chr2:35710646-35710647	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs577827155	chr2:35710648-35710649	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs11124443	chr2:35710649-35710650	Inactive region	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs17016746	chr2:35710661-35710662	Inactive region	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs548233453	chr2:35710667-35710668	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs191149790	chr2:35710701-35710702	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs542196599	chr2:35710717-35710718	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs183361694	chr2:35710751-35710752	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs575484472	chr2:35710798-35710799	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs77612735	chr2:35710886-35710887	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs17016750	chr2:35710894-35710895	Inactive region	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs556221290	chr2:35710944-35710945	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs17016754	chr2:35710967-35710968	Inactive region	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs11675547	chr2:35710969-35710970	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs560321707	chr2:35711029-35711030	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs529279090	chr2:35711058-35711059	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs540113976	chr2:35711117-35711118	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs35971369	chr2:35711136-35711137	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs190484009	chr2:35711150-35711151	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs113360129	chr2:35711182-35711183	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs569137857	chr2:35711193-35711194	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs538098292	chr2:35711194-35711195	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs138389803	chr2:35711207-35711208	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs571443319	chr2:35711227-35711228	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs533909394	chr2:35711255-35711256	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs553821268	chr2:35711277-35711278	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs573599896	chr2:35711296-35711297	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs536244833	chr2:35711355-35711356	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs112184914	chr2:35711358-35711359	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs575545965	chr2:35711376-35711377	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs572020655	chr2:35711418-35711419	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs544477557	chr2:35711431-35711432	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs557960488	chr2:35711468-35711469	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs536374722	chr2:35711470-35711471	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs62143561	chr2:35711471-35711472	Inactive region	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs112973481	chr2:35711492-35711493	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs374212466	chr2:35711496-35711497	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs560632811	chr2:35711507-35711508	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs529324865	chr2:35711513-35711514	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs188148223	chr2:35711517-35711518	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs192733999	chr2:35711546-35711547	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs140738763	chr2:35711551-35711552	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs149776867	chr2:35711563-35711564	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs58358221	chr2:35711566-35711567	Inactive region	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs571508241	chr2:35711567-35711568	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs183404763	chr2:35711568-35711569	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs547225837	chr2:35711586-35711587	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs567362693	chr2:35711609-35711610	ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Breast cancer	21364760	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	18927303	CNVD
Hereditary gingival fibromatosis	19633868	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
Autism	22495309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Medulloblastoma	21163964	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:719 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:35711600-35711800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr2:35720200-35720600	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr2:35720200-35721000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr2:35720200-35721000	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr2:35720200-35721000	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr2:35720200-35721000	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr2:35720200-35721000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr2:35720200-35721200	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr2:35725800-35728000	Enhancers	HUVEC	blood vessel
10	chr2:35726000-35727000	Enhancers	HMEC	breast
11	chr2:35726000-35727200	Enhancers	Hela-S3	cervix
12	chr2:35727000-35728200	Weak transcription	HMEC	breast
13	chr2:35727200-35728400	Weak transcription	Hela-S3	cervix
14	chr2:35727600-35728800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr2:35728000-35728800	Flanking Active TSS	HUVEC	blood vessel
16	chr2:35728000-35730000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr2:35728200-35730400	Enhancers	HMEC	breast
18	chr2:35728400-35729800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr2:35728400-35729800	Enhancers	Hela-S3	cervix
20	chr2:35728600-35729800	Enhancers	NHEK	skin
21	chr2:35728800-35729200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr2:35728800-35729200	Enhancers	HUVEC	blood vessel
23	chr2:35729200-35729400	Flanking Active TSS	HUVEC	blood vessel
24	chr2:35729200-35730400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr2:35729400-35730400	Enhancers	HUVEC	blood vessel
26	chr2:35730400-35733600	Weak transcription	HUVEC	blood vessel
27	chr2:35730400-35735600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr2:35730400-35735600	Weak transcription	HMEC	breast
29	chr2:35733600-35735600	Enhancers	HUVEC	blood vessel
30	chr2:35735600-35736200	Flanking Active TSS	HUVEC	blood vessel
31	chr2:35735600-35736400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr2:35735600-35736400	Enhancers	HMEC	breast
33	chr2:35735800-35736200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr2:35735800-35736200	Enhancers	Adipose Nuclei	Adipose
35	chr2:35735800-35736400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr2:35736200-35736800	Enhancers	HUVEC	blood vessel
37	chr2:35736400-35739800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr2:35739800-35740200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr2:35741000-35743000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr2:35743000-35743800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
41	chr2:35743800-35747600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr2:35743800-35754600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr2:35747000-35748000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr2:35747000-35748200	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr2:35747000-35748200	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr2:35747200-35747800	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr2:35747200-35748000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr2:35747600-35748000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr2:35747800-35748200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
50	chr2:35747800-35748400	Enhancers	HUES6 Cell Line	embryonic stem cell

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