Variant report

Variant	nsv535634
Chromosome Location	chr2:34831613-34986940
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:450)
CpG islands
(count:123)
Chromatin interactive
region (count:5)
LncRNA
region (count:32)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:450 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr2:34902415-34902679	GM12878	blood:	n/a	n/a
2	BATF	chr2:34902921-34903226	GM12878	blood:	n/a	n/a
3	BATF	chr2:34881803-34882061	GM12878	blood:	n/a	n/a
4	BATF	chr2:34902925-34903229	GM12878	blood:	n/a	n/a
5	BHLHE40	chr2:34891473-34891834	GM12878	blood:	n/a	n/a
6	BHLHE40	chr2:34908833-34908941	GM12878	blood:	n/a	n/a
7	BHLHE40	chr2:34963851-34964109	GM12878	blood:	n/a	n/a
8	BHLHE40	chr2:34902255-34902723	GM12878	blood:	n/a	n/a
9	BHLHE40	chr2:34930671-34930923	GM12878	blood:	n/a	n/a
10	CEBPB	chr2:34907939-34908176	A549	lung:	n/a	chr2:34908035-34908046
11	CEBPB	chr2:34850841-34851040	A549	lung:	n/a	chr2:34850939-34850950 chr2:34850903-34850914
12	CEBPB	chr2:34907924-34908188	HepG2	liver:	n/a	chr2:34908035-34908046
13	CEBPB	chr2:34850814-34851079	HepG2	liver:	n/a	chr2:34850939-34850950 chr2:34850903-34850914
14	CEBPB	chr2:34876038-34876081	K562	blood:	n/a	n/a
15	CEBPB	chr2:34960041-34960126	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr2:34840044-34840132	A549	lung:	n/a	n/a
17	CEBPB	chr2:34931219-34931422	HepG2	liver:	n/a	chr2:34931302-34931313
18	CHD1	chr2:34904395-34904596	GM12878	blood:	n/a	n/a
19	CHD1	chr2:34913646-34913857	GM12878	blood:	n/a	n/a
20	CHD1	chr2:34903650-34903710	GM12878	blood:	n/a	n/a
21	CHD1	chr2:34908873-34909006	GM12878	blood:	n/a	n/a
22	CHD1	chr2:34902538-34902913	GM12878	blood:	n/a	n/a
23	CHD2	chr2:34914407-34914412	GM12878	blood:	n/a	n/a
24	CHD2	chr2:34902278-34902563	GM12878	blood:	n/a	n/a
25	CHD2	chr2:34902764-34902800	GM12878	blood:	n/a	n/a
26	CHD2	chr2:34963635-34964103	GM12878	blood:	n/a	n/a
27	CHD2	chr2:34881819-34881970	GM12878	blood:	n/a	n/a
28	CTCF	chr2:34951080-34951409	MCF-7	breast:	n/a	chr2:34951208-34951217 chr2:34951206-34951222 chr2:34951205-34951223 chr2:34951210-34951220 chr2:34951196-34951204 chr2:34951207-34951228
29	CTCF	chr2:34951180-34951330	GM12869	blood:	n/a	chr2:34951208-34951217 chr2:34951206-34951222 chr2:34951205-34951223 chr2:34951210-34951220 chr2:34951196-34951204 chr2:34951207-34951228
30	CTCF	chr2:34963804-34964004	K562	blood:	n/a	chr2:34963821-34963828
31	CTCF	chr2:34944421-34944431	A549	lung:	n/a	n/a
32	CTCF	chr2:34963840-34963990	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr2:34951100-34951250	GM12872	blood:	n/a	chr2:34951208-34951217 chr2:34951206-34951222 chr2:34951205-34951223 chr2:34951210-34951220 chr2:34951196-34951204 chr2:34951207-34951228
34	CTCF	chr2:34963860-34964010	HRPEpiC	eye:	n/a	n/a
35	CTCF	chr2:34951040-34951190	NHEK	skin:	n/a	n/a
36	CTCF	chr2:34930620-34930770	RPTEC	kidney:	n/a	n/a
37	CTCF	chr2:34951060-34951210	HepG2	liver:	n/a	chr2:34951196-34951204
38	CTCF	chr2:34951136-34951230	MCF-7	breast:	n/a	chr2:34951208-34951217 chr2:34951206-34951222 chr2:34951205-34951223 chr2:34951210-34951220 chr2:34951196-34951204 chr2:34951207-34951228
39	CTCF	chr2:34963721-34964239	GM12878	blood:	n/a	chr2:34963821-34963828
40	CTCF	chr2:34963861-34964092	Kidney_OC	kidney:	n/a	n/a
41	CTCF	chr2:34951120-34951270	MCF-7	breast:	n/a	chr2:34951208-34951217 chr2:34951206-34951222 chr2:34951205-34951223 chr2:34951210-34951220 chr2:34951196-34951204 chr2:34951207-34951228
42	CTCF	chr2:34951100-34951250	BE2_C	brain:	n/a	chr2:34951208-34951217 chr2:34951206-34951222 chr2:34951205-34951223 chr2:34951210-34951220 chr2:34951196-34951204 chr2:34951207-34951228
43	CTCF	chr2:34944356-34944490	HepG2	liver:	n/a	n/a
44	CTCF	chr2:34951060-34951210	GM12874	blood:	n/a	chr2:34951196-34951204
45	CTCF	chr2:34913726-34913926	GM12878	blood:	n/a	n/a
46	CTCF	chr2:34963840-34963990	HMF	breast:	n/a	n/a
47	CTCF	chr2:34963860-34964010	GM06990	blood:	n/a	n/a
48	CTCF	chr2:34944340-34944490	RPTEC	kidney:	n/a	n/a
49	CTCF	chr2:34963740-34963990	GM12865	blood:	n/a	chr2:34963821-34963828
50	CTCF	chr2:34963880-34964030	GM12868	blood:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:34902113-34902163	HIPEpiC	eye:	n/a
2	chr2:34902113-34902163	HIPEpiC	eye:	n/a
3	chr2:34852273-34852323	H1-hESC	embryonic stem cell:	embryo
4	chr2:34852273-34852323	GM19239	blood:	n/a
5	chr2:34902113-34902163	PFSK-1	brain:	n/a
6	chr2:34902113-34902163	HCT-116	colon:	n/a
7	chr2:34902113-34902163	HL-60	blood:	n/a
8	chr2:34902113-34902163	AG04449	skin:	fetal
9	chr2:34902113-34902163	RPTEC	kidney:	n/a
10	chr2:34902113-34902163	CMK	blood:	n/a
11	chr2:34852273-34852323	HepG2	liver:	n/a
12	chr2:34902113-34902163	GM06990	blood:	n/a
13	chr2:34902113-34902163	HCM	heart:	n/a
14	chr2:34902113-34902163	K562	blood:	n/a
15	chr2:34902113-34902163	HMEC	breast:	n/a
16	chr2:34852273-34852323	Caco-2	colon:	n/a
17	chr2:34902113-34902163	HCF	heart:	n/a
18	chr2:34852273-34852323	HCPEpiC	choroid plexus:	n/a
19	chr2:34852273-34852323	MCF-7	breast:	n/a
20	chr2:34852273-34852323	HUVEC	blood vessel:	n/a
21	chr2:34902113-34902163	ECC-1	luminal epithelium:	n/a
22	chr2:34852273-34852323	GM06990	blood:	n/a
23	chr2:34852273-34852323	HAEpiC	amniotic membrane:	n/a
24	chr2:34852273-34852323	K562	blood:	n/a
25	chr2:34902113-34902163	ovcar-3	ovarian:	n/a
26	chr2:34852273-34852323	HEK293	kidney:	embryo
27	chr2:34902113-34902163	BE2_C	brain:	n/a
28	chr2:34902113-34902163	GM12892	blood:	n/a
29	chr2:34902113-34902163	NB4	blood:	n/a
30	chr2:34902113-34902163	PrEC	prostate:	n/a
31	chr2:34852273-34852323	AoSMC	blood vessel:	n/a
32	chr2:34852273-34852323	NHBE	bronchial:	n/a
33	chr2:34852273-34852323	AG09319	gingival:	n/a
34	chr2:34852273-34852323	T-47D	breast:	n/a
35	chr2:34852273-34852323	HIPEpiC	eye:	n/a
36	chr2:34902113-34902163	HEK293	kidney:	embryo
37	chr2:34902113-34902163	SK-N-SH_RA	brain:	n/a
38	chr2:34902113-34902163	MCF-7	breast:	n/a
39	chr2:34852273-34852323	CMK	blood:	n/a
40	chr2:34852273-34852323	GM12891	blood:	n/a
41	chr2:34852273-34852323	U87	brain:	n/a
42	chr2:34902113-34902163	PANC-1	pancreas:	n/a
43	chr2:34852273-34852323	HL-60	blood:	n/a
44	chr2:34852273-34852323	HCM	heart:	n/a
45	chr2:34852273-34852323	HEEpiC	esophagus:	n/a
46	chr2:34902113-34902163	AG04450	lung:	fetal
47	chr2:34902113-34902163	T-47D	breast:	n/a
48	chr2:34852273-34852323	HRE	kidney:	n/a
49	chr2:34852273-34852323	NB4	blood:	n/a
50	chr2:34902113-34902163	HRE	kidney:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:34237581..34238416-chr2:34963443..34964247,2	MCF-7	breast:
2	chr2:34876891..34879240-chr2:34886043..34888561,2	K562	blood:
3	chr2:34929052..34931868-chr2:34933062..34935710,2	K562	blood:
4	chr2:34876891..34879240-chr2:34886043..34888561,2	K562	blood:
5	chr2:34929052..34931868-chr2:34933062..34935710,2	K562	blood:

(count:32 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RASGRP3-15	chr2:34909934-34910063	NONHSAT070041
2	lnc-RASGRP3-15	chr2:34878421-34878470	NONHSAT070041
3	lnc-RASGRP3-3	chr2:34860316-34860407	ENSG00000226785
4	lnc-RASGRP3-4	chr2:34957515-34957624	ENSG00000228262.4
5	lnc-RASGRP3-4	chr2:34935519-34935580	ENSG00000228262.4
6	lnc-FAM98A-2	chr2:34960042-34960174	ENSG00000232153
7	lnc-RASGRP3-4	chr2:34935519-34935571	NONHSAT070044
8	lnc-RASGRP3-4	chr2:34962388-34962638	ENSG00000228262.4
9	lnc-RASGRP3-4	chr2:34947066-34950118	NONHSAT070045
10	lnc-RASGRP3-4	chr2:34947066-34947188	ENSG00000228262.4
11	lnc-RASGRP3-4	chr2:34938657-34938840	ENSG00000228262
12	lnc-RASGRP3-4	chr2:34957515-34957624	ENSG00000228262
13	lnc-RASGRP3-4	chr2:34956433-34956605	ENSG00000228262.4
14	lnc-RASGRP3-4	chr2:34947066-34947580	ENSG00000228262.4
15	lnc-RASGRP3-4	chr2:34902711-34902994	NONHSAT070044
16	lnc-RASGRP3-4	chr2:34938646-34938840	ENSG00000228262.4
17	lnc-FAM98A-8	chr2:34919267-34919365	ENSG00000272027.1
18	lnc-RASGRP3-4	chr2:34938646-34938840	ENSG00000228262.4
19	lnc-RASGRP3-4	chr2:34938657-34938840	ENSG00000228262.4
20	lnc-RASGRP3-4	chr2:34959627-34961285	NONHSAT070048
21	lnc-RASGRP3-4	chr2:34962148-34962183	NONHSAT070048
22	lnc-RASGRP3-4	chr2:34938646-34938840	NONHSAT070045
23	lnc-RASGRP3-4	chr2:34962172-34963510	NONHSAT070051
24	lnc-FAM98A-2	chr2:34962148-34962185	ENSG00000232153
25	lnc-FAM98A-8	chr2:34917357-34917552	ENSG00000272027.1
26	lnc-RASGRP3-4	chr2:34960145-34960753	ENSG00000228262.4
27	lnc-RASGRP3-4	chr2:34962388-34962644	ENSG00000228262.4
28	lnc-RASGRP3-4	chr2:34947066-34947186	ENSG00000228262.4
29	lnc-RASGRP3-4	chr2:34929778-34929989	ENSG00000228262.4
30	lnc-RASGRP3-4	chr2:34978401-34978447	NONHSAT070051
31	lnc-RASGRP3-4	chr2:34935518-34935580	NONHSAT070045
32	lnc-RASGRP3-4	chr2:34962388-34963298	ENSG00000228262

No data

Variant related genes	Relation type
ENSG00000272027	TF binding region
ENSG00000232153	TF binding region
ENSG00000228262	TF binding region
ENSG00000272027	CpG island
ENSG00000232153	CpG island
ENSG00000228262	CpG island
ENSG00000228262	chromatin interactions

Extended variants
information (count: 3256 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:3256 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539530573	chr2:34842227-34842228	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs139597932	chr2:34842243-34842244	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs188893148	chr2:34842251-34842252	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs573648068	chr2:34842252-34842253	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs541383207	chr2:34842263-34842264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs181990444	chr2:34842270-34842271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs113212365	chr2:34842322-34842323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs189312181	chr2:34842339-34842340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs6717661	chr2:34842351-34842352	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs563342068	chr2:34842373-34842374	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs532513840	chr2:34842374-34842375	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs545854539	chr2:34842406-34842407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs559127889	chr2:34842431-34842432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs528252808	chr2:34842437-34842438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs76143965	chr2:34842451-34842452	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs568369694	chr2:34842457-34842458	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs35961997	chr2:34842463-34842464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs2030941	chr2:34842489-34842490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs180882883	chr2:34842517-34842518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs530480114	chr2:34842568-34842569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs374877886	chr2:34842646-34842647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs539540530	chr2:34842651-34842652	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs553075232	chr2:34842673-34842674	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs79685243	chr2:34842675-34842676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs535257190	chr2:34842726-34842727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs111439110	chr2:34842739-34842740	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs3037098	chr2:34842740-34842741	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs397733836	chr2:34842744-34842745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs2030940	chr2:34842748-34842749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs2030939	chr2:34842753-34842754	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs560518748	chr2:34842775-34842776	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs189320593	chr2:34860341-34860342	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs558506334	chr2:34860346-34860347	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs139013705	chr2:34860347-34860348	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs544892573	chr2:34860351-34860352	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs564750626	chr2:34860389-34860390	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs572240978	chr2:34860400-34860401	ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
38	rs113714029	chr2:34860414-34860415	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs578098358	chr2:34860438-34860439	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs62163910	chr2:34860439-34860440	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs371435492	chr2:34860483-34860484	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs180765270	chr2:34860484-34860485	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs549777454	chr2:34860507-34860508	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs549168149	chr2:34860517-34860518	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs553943414	chr2:34860525-34860526	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs562506911	chr2:34860532-34860533	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs373715883	chr2:34860537-34860538	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs551291090	chr2:34860551-34860552	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs371466911	chr2:34860552-34860553	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs2091233	chr2:34860586-34860587	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:62)

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	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:154 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:34842200-34842800	Enhancers	Fetal Lung	lung
2	chr2:34860400-34861000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
3	chr2:34875600-34875800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr2:34881800-34882600	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr2:34884400-34890200	Weak transcription	Right Atrium	heart
6	chr2:34885200-34885600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr2:34885800-34886200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr2:34885800-34886200	Enhancers	Fetal Lung	lung
9	chr2:34889000-34890600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr2:34890600-34892000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr2:34891600-34892400	Enhancers	Brain Germinal Matrix	brain
12	chr2:34892000-34892200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr2:34892200-34892600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr2:34892600-34893600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr2:34895400-34895600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr2:34901600-34902400	Enhancers	Liver	Liver
17	chr2:34902400-34902600	Flanking Active TSS	Liver	Liver
18	chr2:34902600-34903000	Enhancers	Pancreas	Pancrea
19	chr2:34902600-34903200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr2:34902600-34904400	Active TSS	Liver	Liver
21	chr2:34903000-34904200	Active TSS	Fetal Kidney	kidney
22	chr2:34908800-34909400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr2:34919400-34919600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr2:34919600-34926000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr2:34926000-34926400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr2:34926000-34926400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr2:34926200-34926600	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr2:34926400-34927800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr2:34926400-34957600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr2:34926600-34927800	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr2:34927800-34928200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
32	chr2:34927800-34928200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr2:34927800-34928400	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr2:34927800-34928400	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr2:34927800-34928400	Enhancers	Pancreas	Pancrea
36	chr2:34928000-34928800	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr2:34928200-34929200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr2:34928200-34929400	Enhancers	Liver	Liver
39	chr2:34929200-34931000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr2:34929400-34930400	Weak transcription	Liver	Liver
41	chr2:34930400-34930800	Active TSS	Liver	Liver
42	chr2:34930800-34931400	Flanking Active TSS	Liver	Liver
43	chr2:34931000-34931400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr2:34931400-34931800	Enhancers	Liver	Liver
45	chr2:34931800-34932200	Weak transcription	Liver	Liver
46	chr2:34932200-34932400	Enhancers	Liver	Liver
47	chr2:34932400-34939000	Weak transcription	Liver	Liver
48	chr2:34939000-34939800	Strong transcription	Liver	Liver
49	chr2:34939800-34952800	Weak transcription	Liver	Liver
50	chr2:34941000-34942400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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