Variant report

Variant	nsv1000416
Chromosome Location	chr2:31424588-31470845
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:696)
CpG islands
(count:1648)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:696 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr2:31441886-31442907	GM12878	blood:	n/a	n/a
2	ATF2	chr2:31456598-31456992	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr2:31456595-31457193	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr2:31456642-31457042	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr2:31442483-31442746	GM12878	blood:	n/a	n/a
6	BATF	chr2:31442515-31442799	GM12878	blood:	n/a	n/a
7	BCL3	chr2:31456641-31457247	A549	lung:	n/a	chr2:31457001-31457014 chr2:31456758-31456766
8	BCLAF1	chr2:31441899-31442872	GM12878	blood:	n/a	n/a
9	BCLAF1	chr2:31456640-31457127	GM12878	blood:	n/a	chr2:31457001-31457014 chr2:31456758-31456766
10	BHLHE40	chr2:31434430-31434614	K562	blood:	n/a	n/a
11	BHLHE40	chr2:31463632-31463876	GM12878	blood:	n/a	n/a
12	BHLHE40	chr2:31430809-31431053	GM12878	blood:	n/a	n/a
13	BHLHE40	chr2:31456662-31457127	GM12878	blood:	n/a	chr2:31457080-31457096
14	BHLHE40	chr2:31440475-31440850	GM12878	blood:	n/a	n/a
15	BHLHE40	chr2:31441900-31442892	GM12878	blood:	n/a	n/a
16	BRCA1	chr2:31456720-31457019	H1-hESC	embryonic stem cell:	n/a	n/a
17	CCNT2	chr2:31456858-31457304	K562	blood:	n/a	chr2:31457137-31457146
18	CEBPB	chr2:31427031-31427326	IMR90	lung:	n/a	chr2:31427167-31427178
19	CEBPB	chr2:31436089-31436493	MCF-7	breast:	n/a	n/a
20	CEBPB	chr2:31458407-31458725	IMR90	lung:	n/a	n/a
21	CEBPB	chr2:31465299-31465479	HepG2	liver:	n/a	chr2:31465356-31465369 chr2:31465356-31465367
22	CEBPB	chr2:31427049-31427251	K562	blood:	n/a	chr2:31427167-31427178
23	CEBPB	chr2:31456573-31456935	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr2:31427020-31427332	HepG2	liver:	n/a	chr2:31427167-31427178
25	CEBPB	chr2:31442574-31442749	A549	lung:	n/a	n/a
26	CEBPB	chr2:31426142-31426190	K562	blood:	n/a	n/a
27	CEBPB	chr2:31426991-31427339	A549	lung:	n/a	chr2:31427167-31427178
28	CEBPZ	chr2:31452816-31452914	HepG2	liver:	n/a	n/a
29	CHD1	chr2:31442065-31442458	GM12878	blood:	n/a	n/a
30	CHD1	chr2:31456869-31457425	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr2:31456890-31456943	HepG2	liver:	n/a	n/a
32	CHD2	chr2:31456531-31457222	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr2:31456757-31457101	GM12878	blood:	n/a	n/a
34	CHD2	chr2:31441888-31442844	GM12878	blood:	n/a	n/a
35	CREB1	chr2:31456527-31457601	H1-hESC	embryonic stem cell:	n/a	n/a
36	CREB1	chr2:31456659-31457229	A549	lung:	n/a	n/a
37	CREB1	chr2:31456683-31457015	A549	lung:	n/a	n/a
38	CREB1	chr2:31456606-31457154	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTBP2	chr2:31456608-31457511	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr2:31456540-31456690	A549	lung:	n/a	n/a
41	CTCF	chr2:31456680-31456830	NHDF-neo	bronchial:	n/a	n/a
42	CTCF	chr2:31456622-31456897	MCF-7	breast:	n/a	n/a
43	CTCF	chr2:31456614-31456876	T-47D	breast:	n/a	n/a
44	CTCF	chr2:31456633-31456947	GM12892	blood:	n/a	n/a
45	CTCF	chr2:31464860-31465010	GM06990	blood:	n/a	n/a
46	CTCF	chr2:31456680-31456830	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr2:31456660-31456810	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr2:31456542-31456974	IMR90	lung:	n/a	n/a
49	CTCF	chr2:31456660-31456810	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr2:31456640-31456790	GM12875	blood:	n/a	n/a

(count:1648 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:31457608-31457658	NB4	blood:	n/a
2	chr2:31457608-31457658	NB4	blood:	n/a
3	chr2:31456741-31456791	GM06990	blood:	n/a
4	chr2:31455443-31455493	T-47D	breast:	n/a
5	chr2:31441554-31441604	HAEpiC	amniotic membrane:	n/a
6	chr2:31456964-31457014	HepG2	liver:	n/a
7	chr2:31456964-31457014	ECC-1	luminal epithelium:	n/a
8	chr2:31458372-31458422	NHDF-neo	bronchial:	n/a
9	chr2:31449901-31449951	Jurkat	blood:	n/a
10	chr2:31456741-31456791	PANC-1	pancreas:	n/a
11	chr2:31441588-31441638	GM12892	blood:	n/a
12	chr2:31441554-31441604	Caco-2	colon:	n/a
13	chr2:31458372-31458422	HAEpiC	amniotic membrane:	n/a
14	chr2:31456761-31456811	AG04449	skin:	fetal
15	chr2:31456789-31456839	U87	brain:	n/a
16	chr2:31439687-31439737	GM06990	blood:	n/a
17	chr2:31456964-31457014	GM12891	blood:	n/a
18	chr2:31456789-31456839	A549	lung:	n/a
19	chr2:31456964-31457014	HRE	kidney:	n/a
20	chr2:31457061-31457111	NB4	blood:	n/a
21	chr2:31440451-31440501	SK-N-MC	brain:	n/a
22	chr2:31441588-31441638	HepG2	liver:	n/a
23	chr2:31458372-31458422	PFSK-1	brain:	n/a
24	chr2:31458372-31458422	NHBE	bronchial:	n/a
25	chr2:31456964-31457014	HRPEpiC	eye:	n/a
26	chr2:31456747-31456797	PANC-1	pancreas:	n/a
27	chr2:31456964-31457014	AoSMC	blood vessel:	n/a
28	chr2:31455443-31455493	CMK	blood:	n/a
29	chr2:31441312-31441362	BE2_C	brain:	n/a
30	chr2:31457058-31457108	NT2-D1	testis:	n/a
31	chr2:31457608-31457658	Hela-S3	cervix:	n/a
32	chr2:31441588-31441638	A549	lung:	n/a
33	chr2:31455443-31455493	AG10803	skin:	n/a
34	chr2:31457058-31457108	HEK293	kidney:	embryo
35	chr2:31449901-31449951	GM12892	blood:	n/a
36	chr2:31456747-31456797	BJ	skin:	n/a
37	chr2:31459843-31459893	HEK293	kidney:	embryo
38	chr2:31456964-31457014	GM06990	blood:	n/a
39	chr2:31457287-31457337	PrEC	prostate:	n/a
40	chr2:31441312-31441362	ProgFib	skin:	n/a
41	chr2:31441588-31441638	GM12891	blood:	n/a
42	chr2:31440349-31440399	HepG2	liver:	n/a
43	chr2:31457043-31457093	HEEpiC	esophagus:	n/a
44	chr2:31441554-31441604	PANC-1	pancreas:	n/a
45	chr2:31458372-31458422	RPTEC	kidney:	n/a
46	chr2:31456761-31456811	MCF10A-Er-Src	breast:	n/a
47	chr2:31456964-31457014	GM12892	blood:	n/a
48	chr2:31457608-31457658	HAEpiC	amniotic membrane:	n/a
49	chr2:31457061-31457111	HRCEpiC	kidney:	n/a
50	chr2:31457043-31457093	AoSMC	blood vessel:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:31437754..31439740-chr2:31441574..31443729,2	MCF-7	breast:
2	chr2:31444034..31446795-chr2:31457220..31458741,2	K562	blood:
3	chr2:31447947..31449893-chr2:31451727..31454184,2	K562	blood:
4	chr2:31456557..31458927-chr2:31463971..31466184,2	MCF-7	breast:
5	chr2:31456683..31458757-chr2:31460645..31462411,2	MCF-7	breast:
6	chr2:31449885..31453472-chr2:31453576..31457663,3	MCF-7	breast:
7	chr2:31457912..31460253-chr2:31482759..31484283,2	MCF-7	breast:
8	chr17:63334973..63335809-chr2:31437485..31438063,2	MCF-7	breast:
9	chr2:31407024..31409183-chr2:31430215..31431751,2	MCF-7	breast:
10	chr2:31449885..31453472-chr2:31453576..31457663,3	MCF-7	breast:
11	chr2:31449978..31452625-chr2:31454988..31456954,2	K562	blood:
12	chr2:31453246..31458582-chr2:31458844..31463834,9	MCF-7	breast:
13	chr2:31418550..31420224-chr2:31425779..31428465,2	K562	blood:
14	chr2:31447947..31449893-chr2:31451727..31454184,2	K562	blood:
15	chr17:58816926..58819384-chr2:31448134..31450659,2	MCF-7	breast:
16	chr2:31437754..31439740-chr2:31441574..31443729,2	MCF-7	breast:
17	chr2:31449978..31452625-chr2:31454988..31456954,2	K562	blood:
18	chr2:31444034..31446795-chr2:31457220..31458741,2	K562	blood:

No data

Variant related genes	Relation type
RNA5SP90	TF binding region
CAPN14	TF binding region
EHD3	TF binding region
RNA5SP90	CpG island
CAPN14	CpG island
EHD3	CpG island
ENSG00000201671	chromatin interactions
ENSG00000013016	chromatin interactions
ENSG00000214711	chromatin interactions

Extended variants
information (count: 2044 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:2044 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527349795	chr2:31424605-31424606	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs541029411	chr2:31424608-31424609	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs560686928	chr2:31424647-31424648	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs116042097	chr2:31424679-31424680	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs749251	chr2:31424693-31424694	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs374726323	chr2:31424694-31424695	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs75525195	chr2:31424696-31424697	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs532338247	chr2:31424718-31424719	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs552440865	chr2:31424769-31424770	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs199800377	chr2:31424778-31424779	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs566170695	chr2:31424792-31424793	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs534770060	chr2:31424807-31424808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs569207325	chr2:31424817-31424818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs548582330	chr2:31424822-31424823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs370282224	chr2:31424829-31424830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs374806823	chr2:31424871-31424872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs537380910	chr2:31424875-31424876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs557219906	chr2:31424881-31424882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs11692905	chr2:31424885-31424886	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs529244918	chr2:31424916-31424917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs182924295	chr2:31424925-31424926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs572120933	chr2:31424937-31424938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs13426142	chr2:31424983-31424984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs375068006	chr2:31424986-31424987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs368305645	chr2:31425007-31425008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs186983715	chr2:31425013-31425014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs375806047	chr2:31425029-31425030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs543780958	chr2:31425050-31425051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs191803963	chr2:31425056-31425057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs370162438	chr2:31425057-31425058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs532403679	chr2:31425058-31425059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs182812741	chr2:31425059-31425060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs372507048	chr2:31425072-31425073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs372292075	chr2:31425083-31425084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs115954418	chr2:31425121-31425122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs542340666	chr2:31425145-31425146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs201740461	chr2:31425162-31425163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs371274408	chr2:31425169-31425170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs116175374	chr2:31425185-31425186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs114059849	chr2:31425192-31425193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs568154834	chr2:31425193-31425194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs141501040	chr2:31425253-31425254	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs187504492	chr2:31425258-31425259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs570819451	chr2:31425264-31425265	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs539709016	chr2:31425281-31425282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs115979180	chr2:31425288-31425289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs193181348	chr2:31425306-31425307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs558320332	chr2:31425332-31425333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs78711778	chr2:31425334-31425335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs554696406	chr2:31425404-31425405	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Cancer	16751803	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	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
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	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
Medulloblastoma	16968546	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Breast cancer	21364760	CNVD
Wilms tumour	21544195	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	18927303	CNVD
Hepatocellular carcinoma	16750200	CNVD
Lung cancer	16740712	CNVD
Hereditary gingival fibromatosis	19633868	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1229 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:31411000-31427400	Weak transcription	Fetal Brain Female	brain
2	chr2:31411200-31436800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr2:31413400-31425600	Weak transcription	Right Ventricle	heart
4	chr2:31417400-31425400	Weak transcription	Primary B cells from peripheral blood	blood
5	chr2:31420800-31430800	Weak transcription	Primary B cells from cord blood	blood
6	chr2:31421200-31429600	Weak transcription	Dnd41	blood
7	chr2:31423400-31436800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr2:31424000-31424800	Strong transcription	Esophagus	oesophagus
9	chr2:31424200-31435800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr2:31424200-31437600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr2:31424800-31428000	Weak transcription	Esophagus	oesophagus
12	chr2:31425200-31425400	Enhancers	Left Ventricle	heart
13	chr2:31425200-31427400	Enhancers	Colon Smooth Muscle	Colon
14	chr2:31425400-31426400	Weak transcription	Left Ventricle	heart
15	chr2:31425400-31427600	Enhancers	Fetal Heart	heart
16	chr2:31425400-31428400	Strong transcription	Primary B cells from peripheral blood	blood
17	chr2:31425600-31428000	Enhancers	Right Ventricle	heart
18	chr2:31425800-31426200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
19	chr2:31426400-31428400	Enhancers	Left Ventricle	heart
20	chr2:31427400-31427600	Enhancers	Fetal Brain Female	brain
21	chr2:31427400-31428200	Enhancers	Brain Angular Gyrus	brain
22	chr2:31427600-31430800	Weak transcription	Fetal Heart	heart
23	chr2:31428000-31428800	Strong transcription	Esophagus	oesophagus
24	chr2:31428000-31429000	Weak transcription	Right Ventricle	heart
25	chr2:31428200-31428600	Enhancers	Primary neutrophils fromperipheralblood	blood
26	chr2:31428400-31430400	Weak transcription	Primary B cells from peripheral blood	blood
27	chr2:31428400-31431200	Weak transcription	Left Ventricle	heart
28	chr2:31428800-31437400	Weak transcription	Esophagus	oesophagus
29	chr2:31429000-31429200	Enhancers	Right Ventricle	heart
30	chr2:31429800-31430200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr2:31430000-31432800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr2:31430200-31441600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr2:31430400-31431600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr2:31430400-31432000	Enhancers	Primary B cells from peripheral blood	blood
35	chr2:31430600-31431000	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr2:31430600-31431000	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr2:31430800-31431200	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr2:31430800-31431400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr2:31430800-31431800	Enhancers	Primary B cells from cord blood	blood
40	chr2:31430800-31432400	Enhancers	Fetal Heart	heart
41	chr2:31431000-31431600	Enhancers	GM12878-XiMat	blood
42	chr2:31431000-31436000	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr2:31431000-31436000	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr2:31431200-31431400	Enhancers	Left Ventricle	heart
45	chr2:31431200-31436000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
46	chr2:31431600-31432600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr2:31431600-31435800	Weak transcription	GM12878-XiMat	blood
48	chr2:31431800-31436800	Weak transcription	Primary B cells from cord blood	blood
49	chr2:31432000-31435800	Weak transcription	Primary B cells from peripheral blood	blood
50	chr2:31432400-31436600	Weak transcription	Fetal Heart	heart

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