Variant report

Variant	nsv949028
Chromosome Location	chr2:31502801-31665108
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2057)
CpG islands
(count:1098)
Chromatin interactive
region (count:54)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:2057 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:31556390-31556746	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:31547188-31547487	HepG2	liver:	n/a	n/a
3	ATF2	chr2:31547072-31547571	GM12878	blood:	n/a	n/a
4	ATF3	chr2:31607548-31608124	A549	lung:	n/a	n/a
5	ATF3	chr2:31607258-31608244	A549	lung:	n/a	n/a
6	ATF3	chr2:31624208-31624915	A549	lung:	n/a	n/a
7	BATF	chr2:31547143-31547468	GM12878	blood:	n/a	n/a
8	BATF	chr2:31506458-31506686	GM12878	blood:	n/a	chr2:31506561-31506572 chr2:31506534-31506545
9	BATF	chr2:31547082-31547428	GM12878	blood:	n/a	n/a
10	BATF	chr2:31607264-31607518	GM12878	blood:	n/a	chr2:31607407-31607417 chr2:31607406-31607417
11	BATF	chr2:31607261-31607537	GM12878	blood:	n/a	chr2:31607407-31607417 chr2:31607406-31607417
12	BCL11A	chr2:31547118-31547464	GM12878	blood:	n/a	n/a
13	BCL3	chr2:31607173-31608244	A549	lung:	n/a	chr2:31607409-31607418
14	BCL3	chr2:31568412-31568707	GM12878	blood:	n/a	n/a
15	BCL3	chr2:31624269-31625045	A549	lung:	n/a	n/a
16	BCL3	chr2:31607419-31608120	A549	lung:	n/a	n/a
17	BCL3	chr2:31624269-31624952	A549	lung:	n/a	n/a
18	BHLHE40	chr2:31541568-31541890	GM12878	blood:	n/a	n/a
19	BHLHE40	chr2:31624781-31624956	A549	lung:	n/a	n/a
20	BRCA1	chr2:31607458-31608012	Hela-S3	cervix:	n/a	n/a
21	CBX3	chr2:31607095-31608068	HCT-116	colon:	n/a	n/a
22	CBX3	chr2:31652572-31653489	HCT-116	colon:	n/a	n/a
23	CEBPB	chr2:31624186-31625025	A549	lung:	n/a	n/a
24	CEBPB	chr2:31602962-31603263	HepG2	liver:	n/a	chr2:31603127-31603138
25	CEBPB	chr2:31582134-31582478	A549	lung:	n/a	chr2:31582294-31582305
26	CEBPB	chr2:31625466-31625643	H1-hESC	embryonic stem cell:	n/a	chr2:31625512-31625523 chr2:31625514-31625525
27	CEBPB	chr2:31550402-31550781	A549	lung:	n/a	chr2:31550574-31550587 chr2:31550575-31550586 chr2:31550574-31550585
28	CEBPB	chr2:31607544-31608224	A549	lung:	n/a	n/a
29	CEBPB	chr2:31552142-31552368	H1-hESC	embryonic stem cell:	n/a	chr2:31552227-31552238
30	CEBPB	chr2:31635932-31636484	Hela-S3	cervix:	n/a	chr2:31636122-31636133
31	CEBPB	chr2:31635987-31636248	HepG2	liver:	n/a	chr2:31636122-31636133
32	CEBPB	chr2:31635826-31636398	A549	lung:	n/a	chr2:31636122-31636133
33	CEBPB	chr2:31583324-31583679	IMR90	lung:	n/a	n/a
34	CEBPB	chr2:31560773-31561135	IMR90	lung:	n/a	n/a
35	CEBPB	chr2:31550433-31550738	K562	blood:	n/a	chr2:31550574-31550587 chr2:31550575-31550586 chr2:31550574-31550585
36	CEBPB	chr2:31556360-31556839	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr2:31607625-31608199	A549	lung:	n/a	n/a
38	CEBPB	chr2:31556484-31556847	HepG2	liver:	n/a	n/a
39	CEBPB	chr2:31557603-31557966	IMR90	lung:	n/a	n/a
40	CEBPB	chr2:31607119-31608244	HCT-116	colon:	n/a	n/a
41	CEBPB	chr2:31556430-31556876	A549	lung:	n/a	n/a
42	CEBPB	chr2:31550430-31550759	IMR90	lung:	n/a	chr2:31550574-31550587 chr2:31550575-31550586 chr2:31550574-31550585
43	CEBPB	chr2:31550374-31550921	MCF-7	breast:	n/a	chr2:31550574-31550587 chr2:31550575-31550586 chr2:31550574-31550585
44	CEBPB	chr2:31645399-31645402	K562	blood:	n/a	n/a
45	CEBPB	chr2:31552229-31552230	HepG2	liver:	n/a	n/a
46	CEBPB	chr2:31607246-31608362	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr2:31607229-31608125	HCT-116	colon:	n/a	n/a
48	CEBPB	chr2:31583369-31583742	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr2:31607277-31608248	IMR90	lung:	n/a	n/a
50	CEBPB	chr2:31556358-31556940	MCF-7	breast:	n/a	n/a

(count:1098 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:31570468-31570518	U87	brain:	n/a
2	chr2:31637849-31637899	HCF	heart:	n/a
3	chr2:31508053-31508103	AG04449	skin:	fetal
4	chr2:31508053-31508103	RPTEC	kidney:	n/a
5	chr2:31607761-31607811	AG04449	skin:	fetal
6	chr2:31637849-31637899	HEK293	kidney:	embryo
7	chr2:31637622-31637672	SK-N-SH	brain:	n/a
8	chr2:31607761-31607811	T-47D	breast:	n/a
9	chr2:31570468-31570518	HMEC	breast:	n/a
10	chr2:31541350-31541400	BJ	skin:	n/a
11	chr2:31526419-31526469	SAEC	small airway:	n/a
12	chr2:31522601-31522651	ovcar-3	ovarian:	n/a
13	chr2:31607761-31607811	Caco-2	colon:	n/a
14	chr2:31541350-31541400	HCF	heart:	n/a
15	chr2:31625013-31625063	AG10803	skin:	n/a
16	chr2:31541350-31541400	BE2_C	brain:	n/a
17	chr2:31558544-31558594	GM12892	blood:	n/a
18	chr2:31526419-31526469	U87	brain:	n/a
19	chr2:31637849-31637899	SK-N-MC	brain:	n/a
20	chr2:31558544-31558594	ProgFib	skin:	n/a
21	chr2:31570468-31570518	HCPEpiC	choroid plexus:	n/a
22	chr2:31541350-31541400	RPTEC	kidney:	n/a
23	chr2:31522601-31522651	BJ	skin:	n/a
24	chr2:31520167-31520217	HRPEpiC	eye:	n/a
25	chr2:31556516-31556566	IMR90	lung:	fetal
26	chr2:31637622-31637672	HIPEpiC	eye:	n/a
27	chr2:31637348-31637398	AG09309	skin:	n/a
28	chr2:31625013-31625063	SKMC	muscle:	n/a
29	chr2:31556516-31556566	ProgFib	skin:	n/a
30	chr2:31605342-31605392	GM06990	blood:	n/a
31	chr2:31559579-31559629	GM12891	blood:	n/a
32	chr2:31638511-31638561	NT2-D1	testis:	n/a
33	chr2:31638511-31638561	HUVEC	blood vessel:	n/a
34	chr2:31541350-31541400	HRCEpiC	kidney:	n/a
35	chr2:31522601-31522651	HAEpiC	amniotic membrane:	n/a
36	chr2:31559579-31559629	HEK293	kidney:	embryo
37	chr2:31625013-31625063	AG04449	skin:	fetal
38	chr2:31637348-31637398	SAEC	small airway:	n/a
39	chr2:31637622-31637672	NHDF-neo	bronchial:	n/a
40	chr2:31605342-31605392	NT2-D1	testis:	n/a
41	chr2:31541350-31541400	GM19239	blood:	n/a
42	chr2:31511030-31511080	GM12891	blood:	n/a
43	chr2:31607761-31607811	BE2_C	brain:	n/a
44	chr2:31637622-31637672	GM06990	blood:	n/a
45	chr2:31559579-31559629	GM06990	blood:	n/a
46	chr2:31607761-31607811	AoSMC	blood vessel:	n/a
47	chr2:31559579-31559629	HEEpiC	esophagus:	n/a
48	chr2:31637622-31637672	NT2-D1	testis:	n/a
49	chr2:31607761-31607811	SKMC	muscle:	n/a
50	chr2:31511030-31511080	H1-hESC	embryonic stem cell:	embryo

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:31375968..31378300-chr2:31551253..31553701,2	MCF-7	breast:
2	chr2:31644783..31646814-chr2:31651303..31655171,3	MCF-7	breast:
3	chr2:31619044..31622000-chr2:31622543..31624849,2	K562	blood:
4	chr2:31648749..31651187-chr2:31653757..31655577,2	MCF-7	breast:
5	chr2:31636957..31637459-chr2:31650773..31651525,2	MCF-7	breast:
6	chr2:31542907..31544508-chr2:31546442..31548990,2	K562	blood:
7	chr2:31619044..31622000-chr2:31622543..31624849,2	K562	blood:
8	chr2:30937017..30937537-chr2:31556075..31557040,2	K562	blood:
9	chr2:31542907..31544508-chr2:31546442..31548990,2	K562	blood:
10	chr2:30936638..30937640-chr2:31555613..31556720,3	MCF-7	breast:
11	chr2:31648749..31651187-chr2:31653757..31655577,2	MCF-7	breast:
12	chr2:31636957..31637459-chr2:31650773..31651525,2	MCF-7	breast:
13	chr2:31540620..31542351-chr2:31549685..31551986,2	MCF-7	breast:
14	chr2:31372563..31374637-chr2:31556201..31557717,2	MCF-7	breast:
15	chr2:31555503..31558332-chr2:31561263..31563974,3	MCF-7	breast:
16	chr2:30884239..30886249-chr2:31553808..31556092,2	K562	blood:
17	chr2:31500916..31502879-chr2:31504188..31506195,2	K562	blood:
18	chr2:31540620..31542351-chr2:31549685..31551986,2	MCF-7	breast:
19	chr2:31538207..31541224-chr2:31542918..31545608,3	K562	blood:
20	chr2:31647816..31650394-chr2:31651121..31653448,2	K562	blood:
21	chr2:31455862..31457393-chr2:31556162..31557106,6	MCF-7	breast:
22	chr2:31374076..31374959-chr2:31556105..31557134,5	MCF-7	breast:
23	chr2:31519075..31520575-chr3:73158434..73161244,2	K562	blood:
24	chr2:31290276..31291052-chr2:31556182..31557050,2	K562	blood:
25	chr2:31084597..31085587-chr2:31556139..31557048,4	MCF-7	breast:
26	chr2:30933909..30935269-chr2:31556183..31557206,10	MCF-7	breast:
27	chr2:30936961..30937589-chr2:31556145..31556832,2	MCF-7	breast:
28	chr2:31636539..31637492-chr2:31657533..31658134,3	MCF-7	breast:
29	chr2:31562048..31564605-chr2:31573622..31576030,2	K562	blood:
30	chr2:31517647..31520271-chr2:31522641..31525033,2	MCF-7	breast:
31	chr2:31647816..31650394-chr2:31651121..31653448,2	K562	blood:
32	chr16:70121442..70121968-chr2:31645598..31646126,2	MCF-7	breast:
33	chr2:31517647..31520271-chr2:31522641..31525033,2	MCF-7	breast:
34	chr2:31500916..31502879-chr2:31504188..31506195,2	K562	blood:
35	chr2:31562048..31564605-chr2:31573622..31576030,2	K562	blood:
36	chr2:31361382..31361934-chr2:31556210..31557022,2	MCF-7	breast:
37	chr2:31538207..31541224-chr2:31542918..31545608,3	K562	blood:
38	chr2:31457063..31459277-chr2:31520684..31522523,2	MCF-7	breast:
39	chr2:31504614..31506974-chr2:31507651..31509290,2	MCF-7	breast:
40	chr2:31456323..31456990-chr2:31537940..31538635,2	MCF-7	breast:
41	chr2:31555503..31558332-chr2:31561263..31563974,3	MCF-7	breast:
42	chr2:31538003..31538887-chr3:63978954..63979735,2	MCF-7	breast:
43	chr2:31495749..31498208-chr2:31503844..31506065,2	MCF-7	breast:
44	chr2:31644783..31646814-chr2:31651303..31655171,3	MCF-7	breast:
45	chr2:31636647..31637404-chr2:31748707..31749593,5	MCF-7	breast:
46	chr2:31566732..31568307-chr2:31571082..31573649,2	MCF-7	breast:
47	chr2:31566732..31568307-chr2:31571082..31573649,2	MCF-7	breast:
48	chr2:31610791..31613346-chr2:31624556..31626809,2	MCF-7	breast:
49	chr2:31609265..31610186-chr2:31954524..31955433,2	MCF-7	breast:
50	chr2:31636673..31637179-chr2:31748776..31749495,2	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	XDH	hsa-miR-26b-5p	chr2:31557858-31557878

Variant related genes	Relation type
ENSG00000213620	TF binding region
XDH	TF binding region
ENSG00000213620	CpG island
XDH	CpG island
ENSG00000158089	chromatin interactions
ENSG00000013016	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000158125	chromatin interactions
ENSG00000214711	chromatin interactions

Extended variants
information (count: 6868 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:6868 , 50 per page) page: 1 2 3 4 5 6 7 ... 138

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10183709	chr2:31502801-31502802	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs10183716	chr2:31502821-31502822	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs376838592	chr2:31502830-31502831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs586245	chr2:31502874-31502875	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs586195	chr2:31502918-31502919	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs7581173	chr2:31502932-31502933	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs555824497	chr2:31502946-31502947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs643137	chr2:31502956-31502957	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs7567147	chr2:31502986-31502987	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs544934609	chr2:31503031-31503032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs643577	chr2:31503066-31503067	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs141714536	chr2:31503099-31503100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs368475538	chr2:31503141-31503142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs550965694	chr2:31503211-31503212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs570969952	chr2:31503217-31503218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs386644503	chr2:31503225-31503226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs584875	chr2:31503226-31503227	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs574161351	chr2:31503284-31503285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs147203437	chr2:31503316-31503317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs556786848	chr2:31503339-31503340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs186392790	chr2:31503354-31503355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs556916200	chr2:31503366-31503367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs138927180	chr2:31503427-31503428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs142923432	chr2:31503446-31503447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs374098629	chr2:31503486-31503487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs583535	chr2:31503492-31503493	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs572522630	chr2:31503513-31503514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs550826066	chr2:31503546-31503547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs35145941	chr2:31503550-31503551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs561261423	chr2:31503563-31503564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs113573469	chr2:31503569-31503570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs563030250	chr2:31503586-31503587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs557823316	chr2:31503642-31503643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562757007	chr2:31503665-31503666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs533609422	chr2:31503671-31503672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs531511466	chr2:31503672-31503673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs139675335	chr2:31503679-31503680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs570888107	chr2:31503703-31503704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs386644504	chr2:31503706-31503707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs582594	chr2:31503707-31503708	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs567270675	chr2:31503736-31503737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs191653052	chr2:31503749-31503750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs148535754	chr2:31503766-31503767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs539829382	chr2:31503846-31503847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs570300134	chr2:31503847-31503848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs373627754	chr2:31503925-31503926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561317008	chr2:31503973-31503974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs572457843	chr2:31503995-31503996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs183530156	chr2:31504021-31504022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs10187343	chr2:31504043-31504044	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:68)

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
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1819 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:31486600-31510000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:31492400-31507800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr2:31492800-31510600	Weak transcription	Aorta	Aorta
4	chr2:31494400-31505600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr2:31495800-31509800	Weak transcription	Esophagus	oesophagus
6	chr2:31497000-31510400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr2:31501400-31505600	Weak transcription	HUVEC	blood vessel
8	chr2:31502000-31505600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr2:31502200-31504200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr2:31502600-31504600	Weak transcription	Placenta	Placenta
11	chr2:31502600-31505400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr2:31504200-31504800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr2:31504600-31512800	Enhancers	Placenta	Placenta
14	chr2:31504800-31505800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr2:31505400-31506400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr2:31505600-31506000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr2:31505600-31506200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr2:31505600-31506200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr2:31505600-31506400	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr2:31505600-31506400	Enhancers	HUVEC	blood vessel
21	chr2:31505800-31506400	Enhancers	NHEK	skin
22	chr2:31505800-31508200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr2:31506000-31507000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr2:31506200-31509000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr2:31506200-31510000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr2:31506400-31508400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr2:31506400-31508800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr2:31506400-31508800	Weak transcription	HUVEC	blood vessel
29	chr2:31507000-31507200	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr2:31507000-31507600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr2:31507000-31507600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr2:31507400-31511000	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr2:31507600-31507800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr2:31507600-31510200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr2:31507800-31510600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr2:31508200-31509400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr2:31508400-31509400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr2:31508800-31511200	Enhancers	NHEK	skin
39	chr2:31508800-31511600	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr2:31508800-31511600	Enhancers	HUVEC	blood vessel
41	chr2:31509000-31509200	Enhancers	H9 Cell Line	embryonic stem cell
42	chr2:31509000-31510200	Enhancers	Fetal Heart	heart
43	chr2:31509000-31510400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr2:31509000-31510600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr2:31509000-31511000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr2:31509000-31511200	Enhancers	HMEC	breast
47	chr2:31509000-31511600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr2:31509200-31511200	Enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr2:31509200-31522000	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr2:31509400-31509600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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