Variant report

Variant	nsv559414
Chromosome Location	chr12:74850206-74931349
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:74902850-74903024	K562	blood:	n/a	n/a
2	ARID3A	chr12:74930983-74931578	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:74930936-74931723	K562	blood:	n/a	n/a
4	BACH1	chr12:74859437-74859442	K562	blood:	n/a	n/a
5	BCL3	chr12:74867773-74868041	GM12878	blood:	n/a	n/a
6	BCLAF1	chr12:74930992-74931946	GM12878	blood:	n/a	chr12:74931769-74931782
7	BHLHE40	chr12:74915689-74915877	K562	blood:	n/a	n/a
8	BHLHE40	chr12:74881949-74882475	GM12878	blood:	n/a	n/a
9	BHLHE40	chr12:74929246-74929640	GM12878	blood:	n/a	n/a
10	BHLHE40	chr12:74931042-74932197	GM12878	blood:	n/a	n/a
11	CBX3	chr12:74902634-74903064	K562	blood:	n/a	n/a
12	CEBPB	chr12:74912268-74912611	HepG2	liver:	n/a	chr12:74912436-74912445 chr12:74912434-74912445 chr12:74912434-74912447 chr12:74912434-74912447 chr12:74912436-74912445 chr12:74912436-74912447 chr12:74912436-74912445 chr12:74912436-74912445
13	CEBPB	chr12:74920359-74920694	H1-hESC	embryonic stem cell:	n/a	chr12:74920521-74920532 chr12:74920523-74920532 chr12:74920523-74920532 chr12:74920523-74920532 chr12:74920521-74920534
14	CEBPB	chr12:74921287-74921669	K562	blood:	n/a	chr12:74921470-74921481
15	CEBPB	chr12:74920378-74920610	MCF-7	breast:	n/a	chr12:74920521-74920532 chr12:74920523-74920532 chr12:74920523-74920532 chr12:74920523-74920532 chr12:74920521-74920534
16	CEBPB	chr12:74920363-74920677	HepG2	liver:	n/a	chr12:74920521-74920532 chr12:74920523-74920532 chr12:74920523-74920532 chr12:74920523-74920532 chr12:74920521-74920534
17	CEBPB	chr12:74919460-74919733	A549	lung:	n/a	chr12:74919566-74919577
18	CEBPB	chr12:74920352-74920629	ECC-1	luminal epithelium:	n/a	chr12:74920521-74920532 chr12:74920523-74920532 chr12:74920523-74920532 chr12:74920523-74920532 chr12:74920521-74920534
19	CEBPB	chr12:74912289-74912594	A549	lung:	n/a	chr12:74912436-74912445 chr12:74912434-74912445 chr12:74912434-74912447 chr12:74912434-74912447 chr12:74912436-74912445 chr12:74912436-74912447 chr12:74912436-74912445 chr12:74912436-74912445
20	CEBPB	chr12:74920349-74920688	K562	blood:	n/a	chr12:74920521-74920532 chr12:74920523-74920532 chr12:74920523-74920532 chr12:74920523-74920532 chr12:74920521-74920534
21	CEBPB	chr12:74920345-74920695	A549	lung:	n/a	chr12:74920521-74920532 chr12:74920523-74920532 chr12:74920523-74920532 chr12:74920523-74920532 chr12:74920521-74920534
22	CEBPB	chr12:74921318-74921664	Hela-S3	cervix:	n/a	chr12:74921470-74921481
23	CEBPB	chr12:74921349-74921599	ECC-1	luminal epithelium:	n/a	chr12:74921470-74921481
24	CEBPB	chr12:74921239-74921741	A549	lung:	n/a	chr12:74921470-74921481
25	CEBPB	chr12:74862181-74862508	HepG2	liver:	n/a	chr12:74862345-74862356
26	CEBPB	chr12:74862177-74862485	A549	lung:	n/a	chr12:74862345-74862356
27	CEBPB	chr12:74912279-74912599	K562	blood:	n/a	chr12:74912436-74912445 chr12:74912434-74912445 chr12:74912434-74912447 chr12:74912434-74912447 chr12:74912436-74912445 chr12:74912436-74912447 chr12:74912436-74912445 chr12:74912436-74912445
28	CEBPB	chr12:74920368-74920615	Hela-S3	cervix:	n/a	chr12:74920521-74920532 chr12:74920523-74920532 chr12:74920523-74920532 chr12:74920523-74920532 chr12:74920521-74920534
29	CEBPB	chr12:74921335-74921625	H1-hESC	embryonic stem cell:	n/a	chr12:74921470-74921481
30	CEBPB	chr12:74865017-74865309	A549	lung:	n/a	n/a
31	CEBPB	chr12:74920342-74920688	IMR90	lung:	n/a	chr12:74920521-74920532 chr12:74920523-74920532 chr12:74920523-74920532 chr12:74920523-74920532 chr12:74920521-74920534
32	CEBPB	chr12:74862249-74862420	HepG2	liver:	n/a	chr12:74862345-74862356
33	CEBPB	chr12:74862197-74862498	K562	blood:	n/a	chr12:74862345-74862356
34	CEBPB	chr12:74921294-74921650	A549	lung:	n/a	chr12:74921470-74921481
35	CEBPB	chr12:74921352-74921586	A549	lung:	n/a	chr12:74921470-74921481
36	CEBPB	chr12:74921293-74921662	HepG2	liver:	n/a	chr12:74921470-74921481
37	CEBPB	chr12:74862173-74862510	IMR90	lung:	n/a	chr12:74862345-74862356
38	CEBPB	chr12:74903165-74903180	K562	blood:	n/a	n/a
39	CEBPB	chr12:74919428-74919738	IMR90	lung:	n/a	chr12:74919566-74919577
40	CEBPB	chr12:74921304-74921652	IMR90	lung:	n/a	chr12:74921470-74921481
41	CEBPB	chr12:74861442-74861518	A549	lung:	n/a	n/a
42	CEBPB	chr12:74862186-74862533	HepG2	liver:	n/a	chr12:74862345-74862356
43	CEBPB	chr12:74919429-74919719	HepG2	liver:	n/a	chr12:74919566-74919577
44	CEBPD	chr12:74862249-74862396	HepG2	liver:	n/a	n/a
45	CHD1	chr12:74931056-74932319	GM12878	blood:	n/a	n/a
46	CHD1	chr12:74931088-74932380	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD1	chr12:74930901-74933411	IMR90	lung:	n/a	n/a
48	CHD2	chr12:74902845-74902925	K562	blood:	n/a	n/a
49	CHD2	chr12:74929332-74929617	HepG2	liver:	n/a	n/a
50	CHD2	chr12:74881981-74882178	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:74931289-74931339	HCF	heart:	n/a
2	chr12:74931289-74931339	HCF	heart:	n/a
3	chr12:74931289-74931339	NH-A	brain:	n/a
4	chr12:74928835-74928885	NH-A	brain:	n/a
5	chr12:74931289-74931339	NHBE	bronchial:	n/a
6	chr12:74931289-74931339	Jurkat	blood:	n/a
7	chr12:74928835-74928885	HCF	heart:	n/a
8	chr12:74928835-74928885	SK-N-MC	brain:	n/a
9	chr12:74931289-74931339	HCPEpiC	choroid plexus:	n/a
10	chr12:74931289-74931339	PANC-1	pancreas:	n/a
11	chr12:74928835-74928885	NHBE	bronchial:	n/a
12	chr12:74928835-74928885	GM12878	blood:	n/a
13	chr12:74928835-74928885	Hela-S3	cervix:	n/a
14	chr12:74928835-74928885	Jurkat	blood:	n/a
15	chr12:74931289-74931339	Caco-2	colon:	n/a
16	chr12:74928835-74928885	HepG2	liver:	n/a
17	chr12:74928835-74928885	AoSMC	blood vessel:	n/a
18	chr12:74928835-74928885	SK-N-SH_RA	brain:	n/a
19	chr12:74931289-74931339	HEK293	kidney:	embryo
20	chr12:74928835-74928885	GM06990	blood:	n/a
21	chr12:74931289-74931339	AoSMC	blood vessel:	n/a
22	chr12:74928835-74928885	NT2-D1	testis:	n/a
23	chr12:74931289-74931339	Hepatocyte	liver:	n/a
24	chr12:74928835-74928885	Hepatocyte	liver:	n/a
25	chr12:74931289-74931339	U87	brain:	n/a
26	chr12:74928835-74928885	GM12891	blood:	n/a
27	chr12:74931289-74931339	ProgFib	skin:	n/a
28	chr12:74931289-74931339	HL-60	blood:	n/a
29	chr12:74928835-74928885	HRCEpiC	kidney:	n/a
30	chr12:74928835-74928885	AG09319	gingival:	n/a
31	chr12:74931289-74931339	MCF-7	breast:	n/a
32	chr12:74931289-74931339	SK-N-SH_RA	brain:	n/a
33	chr12:74928835-74928885	ovcar-3	ovarian:	n/a
34	chr12:74928835-74928885	AG09309	skin:	n/a
35	chr12:74931289-74931339	HUVEC	blood vessel:	n/a
36	chr12:74931289-74931339	BJ	skin:	n/a
37	chr12:74931289-74931339	AG04449	skin:	fetal
38	chr12:74931289-74931339	IMR90	lung:	fetal
39	chr12:74928835-74928885	K562	blood:	n/a
40	chr12:74928835-74928885	HL-60	blood:	n/a
41	chr12:74931289-74931339	H1-hESC	embryonic stem cell:	embryo
42	chr12:74928835-74928885	AG04450	lung:	fetal
43	chr12:74928835-74928885	PFSK-1	brain:	n/a
44	chr12:74928835-74928885	HRPEpiC	eye:	n/a
45	chr12:74928835-74928885	CMK	blood:	n/a
46	chr12:74928835-74928885	NB4	blood:	n/a
47	chr12:74931289-74931339	AG10803	skin:	n/a
48	chr12:74931289-74931339	GM12878	blood:	n/a
49	chr12:74931289-74931339	A549	lung:	n/a
50	chr12:74928835-74928885	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:74886784..74889473-chr12:74901933..74904935,3	MCF-7	breast:
2	chr12:74905173..74906711-chr12:74917835..74920721,2	K562	blood:
3	chr12:74901878..74904719-chr12:74924650..74926216,2	K562	blood:
4	chr12:74901878..74904719-chr12:74924650..74926216,2	K562	blood:
5	chr12:74854045..74856877-chr12:74857073..74859373,2	MCF-7	breast:
6	chr12:74869489..74872190-chr12:74878705..74880923,2	MCF-7	breast:
7	chr12:74912802..74915394-chr12:74916118..74917962,2	K562	blood:
8	chr12:74907509..74911440-chr12:74920218..74923279,3	K562	blood:
9	chr12:74907509..74911440-chr12:74920218..74923279,3	K562	blood:
10	chr12:74914272..74917162-chr12:74919146..74920908,2	MCF-7	breast:
11	chr12:74902868..74904501-chr12:74905941..74907973,2	K562	blood:
12	chr12:74883702..74885504-chr12:74913172..74915992,2	K562	blood:
13	chr12:74855468..74859118-chr12:74859957..74863080,3	MCF-7	breast:
14	chr12:74886784..74889473-chr12:74901933..74904935,3	MCF-7	breast:
15	chr12:74923736..74925423-chr17:57914722..57917441,2	MCF-7	breast:
16	chr12:74855922..74856922-chrX:16789379..16790137,2	HCT-116	colon:
17	chr12:74908557..74911203-chr12:74911419..74914670,3	MCF-7	breast:
18	chr12:74901834..74903505-chr12:74911073..74913080,2	MCF-7	breast:
19	chr12:74905173..74906711-chr12:74917835..74920721,2	K562	blood:
20	chr12:74912802..74915394-chr12:74916118..74917962,2	K562	blood:
21	chr12:74883702..74885504-chr12:74913172..74915992,2	K562	blood:
22	chr12:74886086..74889072-chr12:74890768..74893334,2	K562	blood:
23	chr12:74913004..74915768-chr12:74921096..74922965,2	K562	blood:
24	chr12:74918853..74921690-chr12:74930715..74933088,4	MCF-7	breast:
25	chr12:74886086..74889072-chr12:74890768..74893334,2	K562	blood:
26	chr12:74914272..74917162-chr12:74919146..74920908,2	MCF-7	breast:
27	chr12:74687125..74689371-chr12:74929648..74931476,2	K562	blood:
28	chr12:74904398..74905899-chr12:74909563..74911082,2	MCF-7	breast:
29	chr12:74855468..74859118-chr12:74859957..74863080,3	MCF-7	breast:
30	chr12:74913004..74915768-chr12:74921096..74922965,2	K562	blood:
31	chr12:74905829..74910611-chr12:74911058..74915659,4	K562	blood:
32	chr12:74901834..74903505-chr12:74911073..74913080,2	MCF-7	breast:
33	chr12:74905829..74910611-chr12:74911058..74915659,4	K562	blood:
34	chr12:74908557..74911203-chr12:74911419..74914670,3	MCF-7	breast:
35	chr12:74914017..74916580-chr12:74930054..74932508,2	K562	blood:
36	chr12:74902868..74904501-chr12:74905941..74907973,2	K562	blood:
37	chr12:74926662..74928784-chr12:74930378..74933007,2	K562	blood:
38	chr12:74892365..74894879-chr12:74930250..74931832,2	K562	blood:
39	chr12:74904398..74905899-chr12:74909563..74911082,2	MCF-7	breast:
40	chr12:74920482..74922543-chr12:74935619..74938584,2	MCF-7	breast:
41	chr12:74854045..74856877-chr12:74857073..74859373,2	MCF-7	breast:
42	chr12:74877290..74879814-chr12:74930783..74933713,2	MCF-7	breast:
43	chr12:74901933..74904402-chr12:74929884..74932193,2	K562	blood:
44	chr12:74869489..74872190-chr12:74878705..74880923,2	MCF-7	breast:

Variant related genes	Relation type
ATXN7L3B	TF binding region
ATXN7L3B	CpG island
ENSG00000253719	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000257386	chromatin interactions

Extended variants
information (count: 1799 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:1799 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2365916	chr12:74862011-74862012	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs530708709	chr12:74862078-74862079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs73338742	chr12:74862087-74862088	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs376336498	chr12:74862092-74862093	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs370089122	chr12:74862110-74862111	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs567226517	chr12:74862117-74862118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs2365917	chr12:74862192-74862193	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs190696708	chr12:74862209-74862210	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs566612142	chr12:74862228-74862229	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs376475219	chr12:74862233-74862234	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs558670423	chr12:74862258-74862259	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs569191969	chr12:74862285-74862286	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs66629941	chr12:74862286-74862287	Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs555213764	chr12:74862297-74862298	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs138273774	chr12:74862340-74862341	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs544876523	chr12:74862364-74862365	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs554436579	chr12:74862380-74862381	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs572974315	chr12:74862387-74862388	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs375147575	chr12:74862394-74862395	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs545131823	chr12:74862396-74862397	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs570632185	chr12:74862408-74862409	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs564840130	chr12:74862427-74862428	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs530478329	chr12:74862516-74862517	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs543886997	chr12:74862573-74862574	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs560817109	chr12:74862591-74862592	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs529973156	chr12:74862592-74862593	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs546384395	chr12:74862595-74862596	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs530777396	chr12:74862646-74862647	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs566369725	chr12:74862661-74862662	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs532216082	chr12:74862674-74862675	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs552594176	chr12:74862696-74862697	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs569271393	chr12:74862702-74862703	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs76701975	chr12:74862705-74862706	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs183103246	chr12:74862753-74862754	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs568746200	chr12:74862774-74862775	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs539250870	chr12:74862795-74862796	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs555932364	chr12:74862815-74862816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs143931042	chr12:74862817-74862818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs554399711	chr12:74862876-74862877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs11520220	chr12:74862888-74862889	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs150638189	chr12:74862898-74862899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs187987568	chr12:74862905-74862906	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs56162084	chr12:74862914-74862915	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs560197510	chr12:74862929-74862930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs575259335	chr12:74862947-74862948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs544181143	chr12:74862953-74862954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs75503207	chr12:74862958-74862959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs560853785	chr12:74869406-74869407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs374508326	chr12:74869431-74869432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs184974043	chr12:74869438-74869439	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
craniofacial dysmorphism	21918468	CNVD
Breast cancer	17133270	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	22032731	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:285 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:74862000-74863000	Enhancers	HepG2	liver
2	chr12:74862200-74862800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr12:74862800-74863000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr12:74869400-74871000	Enhancers	Liver	Liver
5	chr12:74871000-74876400	Weak transcription	Liver	Liver
6	chr12:74871200-74871400	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr12:74871200-74871800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr12:74871400-74880000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr12:74874400-74874600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr12:74876200-74877800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
11	chr12:74876400-74877200	Enhancers	Liver	Liver
12	chr12:74877000-74877400	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr12:74877000-74877400	Active TSS	Duodenum Mucosa	Duodenum
14	chr12:74878200-74879000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr12:74878200-74879600	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr12:74878400-74878800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr12:74878600-74879000	Enhancers	Primary hematopoietic stem cells	blood
18	chr12:74878800-74884200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr12:74879000-74884200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr12:74879600-74880000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr12:74879800-74880400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr12:74880000-74880200	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr12:74880000-74880400	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr12:74880200-74884000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
25	chr12:74880400-74885400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr12:74882200-74884200	Enhancers	GM12878-XiMat	blood
27	chr12:74883400-74883600	Enhancers	Primary T helper naive cells from peripheral blood	blood
28	chr12:74883400-74883600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
29	chr12:74883400-74883600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr12:74883400-74883800	Enhancers	Primary T helper cells PMA-I stimulated	--
31	chr12:74883400-74884200	Enhancers	Primary B cells from peripheral blood	blood
32	chr12:74883400-74884200	Enhancers	Dnd41	blood
33	chr12:74883600-74884200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
34	chr12:74883800-74884200	Weak transcription	Primary T helper cells PMA-I stimulated	--
35	chr12:74883800-74884200	Enhancers	Primary T helper cells fromperipheralblood	blood
36	chr12:74884000-74884200	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr12:74884000-74884200	Enhancers	A549	lung
38	chr12:74884200-74884400	Flanking Active TSS	Primary B cells from peripheral blood	blood
39	chr12:74884200-74884400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
40	chr12:74884200-74884400	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
41	chr12:74884200-74884400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr12:74884200-74884600	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
43	chr12:74884200-74884600	Active TSS	Primary T helper cells fromperipheralblood	blood
44	chr12:74884200-74884600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
45	chr12:74884200-74884600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr12:74884200-74884600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr12:74884200-74884600	Active TSS	Duodenum Smooth Muscle	Duodenum
48	chr12:74884200-74884600	Flanking Active TSS	A549	lung
49	chr12:74884200-74884800	Active TSS	Primary B cells from cord blood	blood
50	chr12:74884200-74884800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood

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