Variant report

Variant	rs10877013
Chromosome Location	chr12:58165085-58165086
allele	C/T
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	MXI1	chr12:58164482-58167187	IMR90	lung:	n/a	chr12:58164814-58164829
2	POLR2A	chr12:58165031-58166990	Hela-S3	cervix:	n/a	n/a
3	RUNX3	chr12:58165051-58165415	GM12878	blood:	n/a	n/a
4	TCF12	chr12:58164990-58166916	A549	lung:	n/a	chr12:58165412-58165419
5	POLR2A	chr12:58164350-58167067	K562	blood:	n/a	n/a
6	MAFF	chr12:58164542-58165963	K562	blood:	n/a	chr12:58164809-58164827 chr12:58164815-58164829
7	JUN	chr12:58165005-58167888	K562	blood:	n/a	chr12:58165634-58165643 chr12:58166387-58166396 chr12:58165633-58165646
8	MAFK	chr12:58164486-58166540	K562	blood:	n/a	chr12:58164814-58164830 chr12:58164816-58164826 chr12:58164811-58164826 chr12:58164811-58164822 chr12:58164812-58164832 chr12:58164815-58164829 chr12:58164753-58164770
9	POLR2A	chr12:58165060-58166949	MCF10A-Er-Src	breast:	n/a	n/a
10	EGR1	chr12:58164978-58165239	K562	blood:	n/a	n/a
11	MAZ	chr12:58164980-58166930	IMR90	lung:	n/a	chr12:58166431-58166441
12	POLR2A	chr12:58164078-58166934	H1-hESC	embryonic stem cell:	n/a	n/a
13	CBX3	chr12:58165071-58166837	K562	blood:	n/a	n/a
14	RELA	chr12:58165048-58166218	GM12891	blood:	n/a	n/a
15	MAFK	chr12:58164629-58166568	Hela-S3	cervix:	n/a	chr12:58164814-58164830 chr12:58164816-58164826 chr12:58164811-58164826 chr12:58164811-58164822 chr12:58164812-58164832 chr12:58164815-58164829 chr12:58164753-58164770
16	POLR2A	chr12:58164807-58166735	GM12878	blood:	n/a	n/a
17	POLR2A	chr12:58165013-58166786	GM18951	blood:	n/a	n/a
18	EGR1	chr12:58164979-58165247	K562	blood:	n/a	n/a
19	POLR2A	chr12:58164424-58166975	HepG2	liver:	n/a	n/a
20	RUNX3	chr12:58164988-58166406	GM12878	blood:	n/a	n/a
21	MAX	chr12:58165024-58167098	A549	lung:	n/a	chr12:58166431-58166441
22	MXI1	chr12:58165063-58167795	SK-N-SH	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:58163238..58167741-chr12:58238267..58242135,5	MCF-7	breast:
2	chr12:58164080..58166342-chr12:58209150..58210978,2	K562	blood:
3	chr12:57632502..57635395-chr12:58164755..58167639,2	MCF-7	breast:
4	chr12:57983700..57986584-chr12:58162901..58165594,2	K562	blood:
5	chr12:58163290..58165858-chr12:58229463..58232387,2	K562	blood:
6	chr12:58015127..58017483-chr12:58164900..58167382,2	K562	blood:
7	chr12:58164678..58167264-chr12:58237471..58241552,5	MCF-7	breast:
8	chr12:58164479..58167905-chr12:58237563..58242209,7	K562	blood:
9	chr12:58165013..58167189-chr3:185654127..185656713,2	MCF-7	breast:
10	chr12:58015983..58018978-chr12:58164900..58166825,2	K562	blood:
11	chr12:57823258..57825830-chr12:58164419..58166506,2	MCF-7	breast:
12	chr12:58164836..58167188-chr12:58333922..58337646,3	K562	blood:
13	chr12:58004396..58008788-chr12:58163385..58167140,4	MCF-7	breast:
14	chr12:57911596..57914324-chr12:58165059..58166579,2	MCF-7	breast:
15	chr12:58164894..58167465-chr12:58198689..58202991,3	K562	blood:
16	chr12:57913372..57915977-chr12:58164344..58168645,6	K562	blood:
17	chr12:58165030..58167398-chr12:58198100..58200821,2	MCF-7	breast:
18	chr12:58164032..58167803-chr12:58328284..58330655,5	K562	blood:
19	chr12:57912814..57915992-chr12:58164344..58170030,6	K562	blood:

Variant related genes	Relation type
CYP27B1	TF binding region
METTL21B	TF binding region
ENSG00000257921	TF binding region
METTL1	TF binding region
ENSG00000257698	Chromatin interaction
ENSG00000175197	Chromatin interaction
ENSG00000175215	Chromatin interaction
ENSG00000135502	Chromatin interaction
ENSG00000136527	Chromatin interaction
ENSG00000257953	Chromatin interaction
ENSG00000206749	Chromatin interaction
ENSG00000185633	Chromatin interaction
ENSG00000135407	Chromatin interaction
ENSG00000166896	Chromatin interaction
ENSG00000258001	Chromatin interaction
ENSG00000208028	Chromatin interaction
ENSG00000166908	Chromatin interaction
ENSG00000166987	Chromatin interaction
ENSG00000240771	Chromatin interaction
ENSG00000179912	Chromatin interaction

Extended variants
information (count: 54 )
Associated
traits (count: 34 )

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs1021469	0.88[CEU][hapmap];0.88[JPT][hapmap];0.86[MEX][hapmap];0.88[EUR][1000 genomes]
rs10431505	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10431552	0.96[CEU][hapmap];0.89[CHB][hapmap];0.97[CHD][hapmap];0.96[GIH][hapmap];0.94[JPT][hapmap];0.82[MEX][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10747783	0.96[CEU][hapmap];0.89[CHB][hapmap];0.94[JPT][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10783847	0.87[ASW][hapmap];0.96[CEU][hapmap];0.89[CHB][hapmap];0.97[CHD][hapmap];0.96[GIH][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10783848	0.95[CEU][hapmap];0.88[CHB][hapmap];0.93[JPT][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10877011	0.81[CEU][hapmap];0.85[TSI][hapmap];0.85[EUR][1000 genomes]
rs10877012	0.96[CEU][hapmap];0.89[CHB][hapmap];0.97[CHD][hapmap];0.94[JPT][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10877014	1.00[ASW][hapmap];0.96[CEU][hapmap];0.89[CHB][hapmap];0.97[CHD][hapmap];0.95[GIH][hapmap];0.94[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10877015	0.96[CEU][hapmap];0.89[CHB][hapmap];0.97[CHD][hapmap];0.94[JPT][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10877016	0.96[CEU][hapmap];0.89[CHB][hapmap];0.94[CHD][hapmap];0.96[GIH][hapmap];0.94[JPT][hapmap];0.82[MEX][hapmap];1.00[TSI][hapmap];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10877017	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10877018	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10877019	0.96[CEU][hapmap];0.89[CHB][hapmap];0.97[CHD][hapmap];0.94[JPT][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11172333	0.96[CEU][hapmap];0.89[CHB][hapmap];0.97[CHD][hapmap];0.94[JPT][hapmap];1.00[TSI][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11172335	0.96[CEU][hapmap];0.89[CHB][hapmap];0.97[CHD][hapmap];0.94[JPT][hapmap];1.00[TSI][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11172342	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11172343	0.96[CEU][hapmap];0.89[CHB][hapmap];0.94[JPT][hapmap];0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11172344	0.87[ASW][hapmap];0.96[CEU][hapmap];0.89[CHB][hapmap];0.97[CHD][hapmap];0.96[GIH][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11172349	0.96[CEU][hapmap];0.84[CHB][hapmap];0.92[CHD][hapmap];0.94[JPT][hapmap];1.00[TSI][hapmap];0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11172350	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11172351	0.96[CEU][hapmap];0.84[CHB][hapmap];0.92[CHD][hapmap];0.94[JPT][hapmap];1.00[TSI][hapmap];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1599932	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1875124	0.96[CEU][hapmap];0.89[CHB][hapmap];0.97[CHD][hapmap];0.94[JPT][hapmap];1.00[TSI][hapmap];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1875125	0.81[JPT][hapmap]
rs2014886	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2069502	0.96[CEU][hapmap];0.89[CHB][hapmap];0.91[CHD][hapmap];0.88[JPT][hapmap];0.91[TSI][hapmap];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2069506	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2072052	0.96[CEU][hapmap];0.89[CHB][hapmap];0.92[CHD][hapmap];0.88[JPT][hapmap];0.91[TSI][hapmap];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2291617	0.96[CEU][hapmap];0.94[TSI][hapmap];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3782130	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3825079	0.96[CEU][hapmap];0.84[CHB][hapmap];0.92[CHD][hapmap];0.94[JPT][hapmap];1.00[TSI][hapmap];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4646536	1.00[ASW][hapmap];0.96[CEU][hapmap];0.89[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.95[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4760332	0.81[JPT][hapmap]
rs56177740	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6581155	1.00[ASW][hapmap];0.96[CEU][hapmap];0.89[CHB][hapmap];0.97[CHD][hapmap];0.83[GIH][hapmap];0.94[JPT][hapmap];0.86[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap]
rs701008	0.81[TSI][hapmap]
rs703842	0.94[ASW][hapmap];0.96[CEU][hapmap];0.89[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs724834	0.96[CEU][hapmap];0.89[CHB][hapmap];0.94[JPT][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7489290	0.86[YRI][hapmap]
rs7965287	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs8181644	0.96[CEU][hapmap];0.89[CHB][hapmap];0.97[CHD][hapmap];0.96[GIH][hapmap];0.94[JPT][hapmap];0.82[MEX][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs870392	0.81[JPT][hapmap]
rs871871	0.81[JPT][hapmap]
rs923829	0.96[CEU][hapmap];0.89[CHB][hapmap];0.94[JPT][hapmap];0.80[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9652011	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1038741	chr12:57877355-58174506	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	126 gene(s)	inside rSNPs	diseases
2	nsv541503	chr12:57877355-58174506	Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	126 gene(s)	inside rSNPs	diseases
3	nsv899121	chr12:58079825-58177292	Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
4	nsv559045	chr12:58112189-58165085	Enhancers Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
5	nsv470296	chr12:58112189-58177292	Strong transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
6	nsv510601	chr12:58130298-58191925	Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
7	nsv470297	chr12:58133256-58202419	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription 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	67 gene(s)	inside rSNPs	diseases
8	nsv559046	chr12:58162085-58478598	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	261 gene(s)	inside rSNPs	diseases

mRNA abundance (count:34)

SNP	Gene	Cis/trans	Tissue	Source
rs10877013	TSFM	Cis_1M	lymphoblastoid	RTeQTL
rs10877013	FAM119B	cis	Frontal Cortex	GTEx
rs10877013	METTL21B	cis	lung	GTEx
rs10877013	TSFM	cis	cerebellum	SCAN
rs10877013	METTL21B	cis	Adipose Subcutaneous	GTEx
rs10877013	METTL21B	cis	Muscle Skeletal	GTEx
rs10877013	KRT5	cis	cerebellum	SCAN
rs10877013	DKFZP586D0919	cis	multi-tissue	Pritchard
rs10877013	FAM119B	cis	lymphoblastoid	seeQTL
rs10877013	METTL21B	cis	Heart Left Ventricle	GTEx
rs10877013	WIBG	cis	cerebellum	SCAN
rs10877013	FAM119B	cis	cerebellum	SCAN
rs10877013	METTL21B	cis	Esophagus Muscularis	GTEx
rs10877013	GPR84	cis	cerebellum	SCAN
rs10877013	TSPAN31	cis	cerebellum	SCAN
rs10877013	FAM119B	cis	Cerebellum	GTEx
rs10877013	TSFM	cis	lymphoblastoid	seeQTL
rs10877013	METTL21B	cis	Whole Blood	GTEx
rs10877013	FAM119B	cis	Brain Pons	GTEx
rs10877013	TSFM	cis	Muscle Skeletal	GTEx
rs10877013	FAM119B	cis	parietal	SCAN
rs10877013	FAM119B	Cis_1M	lymphoblastoid	RTeQTL
rs10877013	CDK2	cis	parietal	SCAN
rs10877013	KIAA0748	cis	cerebellum	SCAN
rs10877013	METTL21B	cis	Esophagus Mucosa	GTEx
rs10877013	TSFM	cis	multi-tissue	Pritchard
rs10877013	METTL21B	cis	Skin Sun Exposed Lower leg	GTEx
rs10877013	TSPAN31	cis	parietal	SCAN
rs10877013	XRCC6BP1	cis	Whole Blood	GTEx
rs10877013	ESPL1	cis	parietal	SCAN
rs10877013	XRCC6BP1	cis	lymphoblastoid	seeQTL
rs10877013	HSD17B6	cis	cerebellum	SCAN
rs10877013	CDK4	cis	cerebellum	SCAN
rs10877013	XRCC6BP1	cis	Muscle Skeletal	GTEx

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:58160800-58165200	Weak transcription	Brain Substantia Nigra	brain
2	chr12:58161000-58165200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr12:58161000-58165200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr12:58161000-58165200	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr12:58161200-58165200	Weak transcription	Brain Cingulate Gyrus	brain
6	chr12:58161400-58165200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr12:58161400-58165200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr12:58161400-58165200	Weak transcription	Colonic Mucosa	Colon
9	chr12:58162200-58165200	Weak transcription	Fetal Brain Male	brain
10	chr12:58162800-58165200	Weak transcription	Thymus	Thymus
11	chr12:58163200-58165200	Weak transcription	Brain Hippocampus Middle	brain
12	chr12:58163400-58165200	Weak transcription	Brain Angular Gyrus	brain
13	chr12:58163600-58165200	Weak transcription	Brain Anterior Caudate	brain
14	chr12:58163800-58165200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr12:58163800-58165400	Weak transcription	Aorta	Aorta
16	chr12:58164000-58165200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr12:58164000-58165200	Weak transcription	Ovary	ovary
18	chr12:58164400-58165200	Enhancers	Primary B cells from peripheral blood	blood
19	chr12:58164400-58165200	Genic enhancers	Skeletal Muscle Female	skeletal muscle
20	chr12:58164600-58165200	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr12:58164600-58165200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
22	chr12:58164600-58165200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr12:58164600-58165200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
24	chr12:58164600-58165200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr12:58164600-58165200	Enhancers	Duodenum Smooth Muscle	Duodenum
26	chr12:58164600-58165200	Enhancers	Esophagus	oesophagus
27	chr12:58164600-58165200	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
28	chr12:58164600-58165200	Genic enhancers	Fetal Muscle Trunk	muscle
29	chr12:58164600-58165200	Enhancers	Fetal Thymus	thymus
30	chr12:58164600-58165200	Enhancers	Left Ventricle	heart
31	chr12:58164600-58165200	Enhancers	Right Atrium	heart
32	chr12:58164600-58165400	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr12:58164600-58165600	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr12:58164600-58165600	Enhancers	Spleen	Spleen
35	chr12:58164600-58165800	Flanking Active TSS	Duodenum Mucosa	Duodenum
36	chr12:58164800-58165200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr12:58164800-58165200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr12:58164800-58165200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr12:58164800-58165200	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr12:58164800-58165200	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
41	chr12:58164800-58165200	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr12:58164800-58165200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr12:58164800-58165200	Active TSS	Colon Smooth Muscle	Colon
44	chr12:58164800-58165200	Genic enhancers	Fetal Intestine Large	intestine
45	chr12:58164800-58165200	Enhancers	Placenta	Placenta
46	chr12:58164800-58165200	Genic enhancers	Fetal Stomach	stomach
47	chr12:58164800-58165200	Enhancers	Placenta Amnion	Placenta Amnion
48	chr12:58164800-58165200	Enhancers	Rectal Mucosa Donor 31	rectum
49	chr12:58164800-58165200	Genic enhancers	Skeletal Muscle Male	skeletal muscle
50	chr12:58164800-58165200	Flanking Active TSS	A549	lung

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