Variant report

Variant	rs2238155
Chromosome Location	chr12:120667194-120667195
allele	A/C
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	MYC	chr12:120666112-120667610	K562	blood:	n/a	chr12:120667115-120667125
2	POLR2A	chr12:120665661-120670391	PANC-1	pancreas:	n/a	n/a
3	NFIC	chr12:120666095-120668191	ECC-1	luminal epithelium:	n/a	chr12:120667168-120667185 chr12:120667169-120667185
4	BHLHE40	chr12:120666783-120667441	K562	blood:	n/a	n/a
5	MAX	chr12:120666182-120667463	K562	blood:	n/a	chr12:120667115-120667125
6	PML	chr12:120666920-120667422	K562	blood:	n/a	n/a
7	POLR2A	chr12:120667095-120669707	Hela-S3	cervix:	n/a	n/a
8	POLR2A	chr12:120665412-120667696	HepG2	liver:	n/a	n/a
9	MYC	chr12:120666131-120667619	K562	blood:	n/a	chr12:120667115-120667125
10	ZBTB7A	chr12:120666077-120667270	ECC-1	luminal epithelium:	n/a	n/a
11	MAX	chr12:120666946-120667274	K562	blood:	n/a	chr12:120667115-120667125
12	GATA2	chr12:120666869-120667376	K562	blood:	n/a	chr12:120667027-120667034 chr12:120667031-120667042
13	POLR2A	chr12:120665367-120669884	H1-hESC	embryonic stem cell:	n/a	n/a
14	REST	chr12:120667027-120667252	K562	blood:	n/a	chr12:120667161-120667171 chr12:120667064-120667077
15	ETS1	chr12:120666977-120667280	K562	blood:	n/a	n/a
16	POLR2A	chr12:120666886-120670873	HUVEC	blood vessel:	n/a	n/a
17	TEAD4	chr12:120666062-120667691	ECC-1	luminal epithelium:	n/a	chr12:120666897-120666906
18	TRIM28	chr12:120666880-120667425	K562	blood:	n/a	n/a
19	SP1	chr12:120666079-120667358	H1-hESC	embryonic stem cell:	n/a	chr12:120667062-120667071 chr12:120666838-120666852 chr12:120667055-120667069 chr12:120667061-120667071 chr12:120667060-120667072
20	NR2F2	chr12:120666673-120668102	MCF-7	breast:	n/a	n/a
21	POLR2A	chr12:120661126-120671187	PANC-1	pancreas:	n/a	n/a
22	STAT5A	chr12:120666916-120667314	K562	blood:	n/a	n/a
23	MYBL2	chr12:120666969-120667445	HepG2	liver:	n/a	n/a
24	TEAD4	chr12:120666062-120667605	K562	blood:	n/a	chr12:120666897-120666906
25	NR2F2	chr12:120666875-120667563	K562	blood:	n/a	n/a
26	RAD21	chr12:120665564-120667381	SK-N-SH	brain:	n/a	chr12:120666316-120666329 chr12:120666912-120666921 chr12:120666536-120666549 chr12:120666313-120666332 chr12:120665696-120665706 chr12:120666318-120666330 chr12:120666318-120666328 chr12:120666317-120666326 chr12:120667153-120667166
27	JUN	chr12:120666044-120669974	K562	blood:	n/a	chr12:120669237-120669248 chr12:120669587-120669598 chr12:120669237-120669249 chr12:120669242-120669249 chr12:120669239-120669247
28	RAD21	chr12:120665831-120667428	HCT-116	colon:	n/a	chr12:120666316-120666329 chr12:120666912-120666921 chr12:120666536-120666549 chr12:120666313-120666332 chr12:120666318-120666330 chr12:120666318-120666328 chr12:120666317-120666326 chr12:120667153-120667166
29	POLR2A	chr12:120666842-120667569	K562	blood:	n/a	n/a
30	SIX5	chr12:120666880-120670022	A549	lung:	n/a	n/a
31	JUND	chr12:120666727-120667539	K562	blood:	n/a	n/a
32	NFIC	chr12:120666265-120667982	ECC-1	luminal epithelium:	n/a	chr12:120667168-120667185 chr12:120667169-120667185
33	MXI1	chr12:120665493-120667376	HepG2	liver:	n/a	chr12:120666690-120666699
34	MAZ	chr12:120666117-120667728	K562	blood:	n/a	chr12:120667115-120667125
35	TEAD4	chr12:120666127-120667214	H1-hESC	embryonic stem cell:	n/a	chr12:120666897-120666906
36	ARID3A	chr12:120666854-120667539	K562	blood:	n/a	n/a
37	CTCF	chr12:120667120-120667270	HAc	cerebellar:	n/a	n/a
38	MAX	chr12:120665977-120669019	MCF-7	breast:	n/a	chr12:120667115-120667125
39	POLR2A	chr12:120666943-120667827	U87	brain:	n/a	n/a
40	GATA3	chr12:120666622-120667381	T-47D	breast:	n/a	chr12:120667027-120667034 chr12:120667031-120667042
41	TEAD4	chr12:120666160-120667423	K562	blood:	n/a	chr12:120666897-120666906
42	RCOR1	chr12:120666814-120667322	K562	blood:	n/a	n/a
43	POLR2A	chr12:120666020-120668914	ECC-1	luminal epithelium:	n/a	n/a
44	YY1	chr12:120666550-120667330	H1-hESC	embryonic stem cell:	n/a	n/a
45	MAX	chr12:120665949-120667424	MCF-7	breast:	n/a	chr12:120667115-120667125
46	TEAD4	chr12:120666559-120667199	H1-hESC	embryonic stem cell:	n/a	chr12:120666897-120666906
47	CEBPD	chr12:120666812-120667787	K562	blood:	n/a	n/a
48	ZBTB7A	chr12:120666806-120667378	K562	blood:	n/a	n/a
49	EP300	chr12:120666858-120669846	A549	lung:	n/a	chr12:120668327-120668337 chr12:120668865-120668875
50	IRF1	chr12:120666989-120667574	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:120665103..120667873-chr12:120713460..120715330,2	K562	blood:
2	chr12:120665534..120667593-chr12:120905328..120907519,2	MCF-7	breast:
3	chr12:120663104..120670865-chr12:120700603..120705016,22	K562	blood:
4	chr12:120642171..120684465-chr12:120719749..120734210,267	K562	blood:
5	chr12:120628211..120641965-chr12:120660551..120674110,39	K562	blood:
6	chr12:120665225..120667778-chr12:120932548..120934846,2	MCF-7	breast:
7	chr12:120665699..120667600-chr12:120702688..120704213,51	MCF-7	breast:
8	chr12:120666210..120668023-chr12:120753232..120755603,3	K562	blood:
9	chr12:120665810..120667921-chr12:120703066..120704397,37	K562	blood:
10	chr12:120666355..120667199-chr12:120728970..120730232,5	MCF-7	breast:
11	chr12:120656223..120689871-chr12:120720394..120738112,311	MCF-7	breast:
12	chr12:120657004..120683911-chr12:120723753..120737731,232	K562	blood:
13	chr12:120666353..120667903-chr12:120793999..120796397,2	MCF-7	breast:
14	chr12:120666758..120668423-chr12:120697948..120699928,2	K562	blood:
15	chr12:120665672..120667688-chr12:120702681..120704360,24	MCF-7	breast:
16	chr1:109821837..109824011-chr12:120666607..120668515,2	MCF-7	breast:
17	chr11:62435015..62436981-chr12:120666928..120669201,2	MCF-7	breast:
18	chr12:120666061..120668017-chr7:7678745..7680697,2	MCF-7	breast:
19	chr12:120426597..120428714-chr12:120665312..120668782,3	MCF-7	breast:
20	chr12:120666983..120668561-chr12:120740491..120742036,2	MCF-7	breast:
21	chr12:120425252..120427815-chr12:120666587..120668265,2	K562	blood:
22	chr12:120666386..120669615-chr12:120738520..120741950,4	K562	blood:
23	chr12:120665350..120668266-chr12:120761295..120765211,4	MCF-7	breast:
24	chr12:120666487..120668568-chr12:120709814..120712269,2	K562	blood:
25	chr12:120426429..120428647-chr12:120666320..120668878,2	MCF-7	breast:

Variant related genes	Relation type
PXN	TF binding region
ENSG00000135127	Chromatin interaction
ENSG00000123009	Chromatin interaction
ENSG00000202538	Chromatin interaction
ENSG00000106399	Chromatin interaction
ENSG00000089159	Chromatin interaction
ENSG00000111786	Chromatin interaction
ENSG00000219545	Chromatin interaction
ENSG00000170890	Chromatin interaction
ENSG00000200795	Chromatin interaction
ENSG00000255857	Chromatin interaction
ENSG00000089163	Chromatin interaction
ENSG00000088986	Chromatin interaction
ENSG00000248008	Chromatin interaction
ENSG00000089154	Chromatin interaction
ENSG00000089157	Chromatin interaction

Extended variants
information (count: 73 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs10437836	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11065035	0.92[CEU][hapmap];0.90[CHB][hapmap];0.95[JPT][hapmap];0.84[EUR][1000 genomes]
rs11065036	0.92[CEU][hapmap];0.90[CHB][hapmap];0.90[CHD][hapmap];0.96[GIH][hapmap];0.95[JPT][hapmap];0.94[MEX][hapmap];0.96[TSI][hapmap];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1151824	0.95[CHB][hapmap];0.83[CHD][hapmap];0.86[JPT][hapmap];0.82[ASN][1000 genomes]
rs1151825	0.95[CHB][hapmap];0.83[CHD][hapmap];0.86[JPT][hapmap];0.82[ASN][1000 genomes]
rs1151827	0.95[CHB][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs1151830	0.84[ASN][1000 genomes]
rs1151832	0.82[CHB][hapmap];0.86[JPT][hapmap];0.81[ASN][1000 genomes]
rs1151837	0.81[CHB][hapmap];0.86[JPT][hapmap];0.80[ASN][1000 genomes]
rs1182860	0.82[ASN][1000 genomes]
rs11833158	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11836049	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1183781	0.94[CHB][hapmap];0.89[JPT][hapmap];0.83[ASN][1000 genomes]
rs12305184	0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12306075	0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12310433	0.92[CEU][hapmap];0.90[CHB][hapmap];0.95[JPT][hapmap];0.84[EUR][1000 genomes]
rs12312562	0.92[CEU][hapmap];0.90[CHB][hapmap];0.90[CHD][hapmap];0.87[GIH][hapmap];0.95[JPT][hapmap];0.88[MEX][hapmap];0.96[TSI][hapmap];0.84[EUR][1000 genomes]
rs12320253	0.88[EUR][1000 genomes]
rs12321884	0.89[ASN][1000 genomes]
rs12578300	0.90[EUR][1000 genomes]
rs12581983	0.87[ASN][1000 genomes]
rs1634814	0.95[CHB][hapmap];0.83[CHD][hapmap];0.86[JPT][hapmap];0.83[ASN][1000 genomes]
rs1634815	0.81[ASN][1000 genomes]
rs2074540	0.92[CEU][hapmap];0.90[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.94[MEX][hapmap];0.96[TSI][hapmap];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2240312	0.85[CHB][hapmap];0.83[CHD][hapmap];0.91[JPT][hapmap]
rs2240315	0.92[CEU][hapmap];0.80[EUR][1000 genomes]
rs2240317	0.92[CEU][hapmap];0.90[CHB][hapmap];0.90[CHD][hapmap];0.87[GIH][hapmap];0.95[JPT][hapmap];0.88[MEX][hapmap];0.96[TSI][hapmap];0.84[EUR][1000 genomes]
rs2240318	0.92[CEU][hapmap];0.90[CHB][hapmap];0.88[CHD][hapmap];0.87[GIH][hapmap];0.95[JPT][hapmap];0.88[MEX][hapmap];0.96[TSI][hapmap];0.86[EUR][1000 genomes]
rs2240319	0.86[EUR][1000 genomes]
rs2240320	0.85[EUR][1000 genomes]
rs2240321	0.92[CEU][hapmap];0.90[CHB][hapmap];0.93[CHD][hapmap];0.96[GIH][hapmap];0.95[JPT][hapmap];0.88[MEX][hapmap];0.96[TSI][hapmap];0.86[EUR][1000 genomes]
rs2240322	0.92[CEU][hapmap];0.90[CHB][hapmap];0.93[CHD][hapmap];0.96[GIH][hapmap];0.95[JPT][hapmap];0.94[MEX][hapmap];0.96[TSI][hapmap];0.86[EUR][1000 genomes]
rs2240323	0.92[CEU][hapmap];0.90[CHB][hapmap];0.93[CHD][hapmap];0.96[GIH][hapmap];0.95[JPT][hapmap];0.83[MEX][hapmap];0.93[TSI][hapmap];0.85[EUR][1000 genomes]
rs2240325	0.92[CEU][hapmap];0.90[CHB][hapmap];0.91[JPT][hapmap];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2269940	0.92[CEU][hapmap];0.96[TSI][hapmap]
rs2269941	0.92[CEU][hapmap];0.90[CHB][hapmap];0.93[CHD][hapmap];0.96[GIH][hapmap];0.95[JPT][hapmap];0.88[MEX][hapmap];0.96[TSI][hapmap];0.80[EUR][1000 genomes]
rs2269943	0.80[EUR][1000 genomes]
rs2269944	0.92[CEU][hapmap];0.90[CHB][hapmap];0.95[JPT][hapmap];0.86[EUR][1000 genomes]
rs2269945	0.92[CEU][hapmap];0.89[CHB][hapmap];0.93[CHD][hapmap];0.93[GIH][hapmap];0.95[JPT][hapmap];0.88[MEX][hapmap];0.96[TSI][hapmap];0.92[EUR][1000 genomes]
rs2283362	0.92[CEU][hapmap];0.82[CHB][hapmap];0.86[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.89[MEX][hapmap];0.93[TSI][hapmap];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2283364	0.90[CHB][hapmap];0.91[JPT][hapmap];0.89[ASN][1000 genomes]
rs2286044	0.92[CEU][hapmap]
rs2286045	0.82[EUR][1000 genomes]
rs2286049	0.92[CEU][hapmap];0.90[CHB][hapmap];0.81[GIH][hapmap];0.95[JPT][hapmap];0.85[TSI][hapmap];0.86[EUR][1000 genomes]
rs2286050	0.92[CEU][hapmap];0.90[CHB][hapmap];0.93[CHD][hapmap];0.96[GIH][hapmap];0.95[JPT][hapmap];0.94[MEX][hapmap];0.96[TSI][hapmap];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2286051	0.90[CHB][hapmap];0.95[JPT][hapmap];0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2422	0.81[JPT][hapmap]
rs3742039	0.95[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs3759397	0.86[YRI][hapmap]
rs3815210	0.80[EUR][1000 genomes]
rs3888586	0.86[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs4522230	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs57546423	0.81[EUR][1000 genomes]
rs59601514	0.90[EUR][1000 genomes]
rs60271600	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7133235	0.91[EUR][1000 genomes]
rs7134706	0.92[CEU][hapmap];0.90[CHB][hapmap];0.90[CHD][hapmap];0.96[GIH][hapmap];0.95[JPT][hapmap];0.94[MEX][hapmap];0.96[TSI][hapmap];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7135914	0.93[EUR][1000 genomes]
rs7294892	0.82[EUR][1000 genomes]
rs7296380	0.90[CHB][hapmap];0.85[CHD][hapmap];0.95[JPT][hapmap];0.80[ASN][1000 genomes]
rs7299429	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7398775	0.83[ASN][1000 genomes]
rs7960120	0.87[ASN][1000 genomes]
rs7978061	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7978175	0.87[EUR][1000 genomes]
rs9630281	0.91[EUR][1000 genomes]
rs9651914	0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv899555	chr12:120519124-120840522	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	499 gene(s)	inside rSNPs	diseases
2	nsv519657	chr12:120533696-120676090	Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
3	nsv560433	chr12:120533696-120676090	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
4	nsv832530	chr12:120586069-120758175	Flanking Active TSS Strong transcription Enhancers Genic enhancers Weak transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	484 gene(s)	inside rSNPs	diseases
5	nsv1035698	chr12:120645330-120777580	Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	436 gene(s)	inside rSNPs	diseases
6	nsv1047447	chr12:120645330-120808621	Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Enhancers Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	436 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs2238155	PLA2G1B	cis	multi-tissue	Pritchard
rs2238155	NME2P1	cis	cerebellum	SCAN
rs2238155	FBXO21	cis	parietal	SCAN
rs2238155	GCN1L1	cis	multi-tissue	Pritchard

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:120663400-120668600	Weak transcription	Fetal Brain Female	brain
2	chr12:120664400-120667600	Weak transcription	Aorta	Aorta
3	chr12:120664400-120675800	Enhancers	Stomach Mucosa	stomach
4	chr12:120664600-120668800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
5	chr12:120665000-120671600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr12:120665200-120692000	Enhancers	Placenta	Placenta
7	chr12:120665400-120667200	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr12:120665400-120667200	Enhancers	HUVEC	blood vessel
9	chr12:120665400-120669000	Flanking Active TSS	HepG2	liver
10	chr12:120665400-120669200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr12:120665400-120669400	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr12:120665400-120670600	Enhancers	Sigmoid Colon	Sigmoid Colon
13	chr12:120665400-120671000	Enhancers	Fetal Thymus	thymus
14	chr12:120665400-120671200	Enhancers	Pancreas	Pancrea
15	chr12:120665400-120673200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr12:120665400-120674200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr12:120665400-120676800	Enhancers	Fetal Heart	heart
18	chr12:120665400-120682200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
19	chr12:120665600-120667600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr12:120665600-120668400	Flanking Active TSS	Stomach Smooth Muscle	stomach
21	chr12:120665600-120668400	Flanking Active TSS	A549	lung
22	chr12:120665600-120670400	Transcr. at gene 5' and 3'	NHEK	skin
23	chr12:120665600-120670600	Enhancers	Gastric	stomach
24	chr12:120665600-120673800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr12:120665600-120674200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr12:120665600-120674200	Enhancers	Fetal Lung	lung
27	chr12:120665600-120675400	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr12:120665600-120682200	Enhancers	Left Ventricle	heart
29	chr12:120665800-120667200	Flanking Active TSS	HSMM	muscle
30	chr12:120665800-120667400	Bivalent Enhancer	Primary B cells from peripheral blood	blood
31	chr12:120665800-120667400	Enhancers	Thymus	Thymus
32	chr12:120665800-120668000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
33	chr12:120665800-120668200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr12:120665800-120668200	Enhancers	Pancreatic Islets	Pancreatic Islet
35	chr12:120665800-120668400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr12:120665800-120668600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr12:120665800-120668600	Enhancers	Primary hematopoietic stem cells	blood
38	chr12:120665800-120668600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr12:120665800-120669200	Flanking Active TSS	Colon Smooth Muscle	Colon
40	chr12:120665800-120670400	Enhancers	Fetal Stomach	stomach
41	chr12:120665800-120670800	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr12:120665800-120670800	Enhancers	Esophagus	oesophagus
43	chr12:120665800-120671000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr12:120665800-120671200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr12:120665800-120673600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
46	chr12:120665800-120674000	Enhancers	H1 Cell Line	embryonic stem cell
47	chr12:120665800-120674400	Enhancers	Psoas Muscle	Psoas
48	chr12:120665800-120675400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
49	chr12:120666000-120667200	Enhancers	Dnd41	blood
50	chr12:120666000-120667400	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood

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