Variant report

Variant	rs1617156
Chromosome Location	chr12:123590165-123590166
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	MYC	chr12:123590140-123590269	MCF10A-Er-Src	breast:	n/a	n/a
2	TCF12	chr12:123589748-123590672	ECC-1	luminal epithelium:	n/a	chr12:123590157-123590164
3	POLR2A	chr12:123589765-123590335	Hela-S3	cervix:	n/a	n/a
4	TCF12	chr12:123590065-123590253	H1-hESC	embryonic stem cell:	n/a	chr12:123590157-123590164
5	STAT3	chr12:123589900-123590383	MCF10A-Er-Src	breast:	n/a	n/a
6	MAX	chr12:123589909-123590759	ECC-1	luminal epithelium:	n/a	n/a
7	CREB1	chr12:123589882-123590464	ECC-1	luminal epithelium:	n/a	n/a
8	FOS	chr12:123590069-123590332	MCF10A-Er-Src	breast:	n/a	chr12:123590111-123590120
9	FOS	chr12:123590080-123590336	MCF10A-Er-Src	breast:	n/a	chr12:123590111-123590120
10	NFIC	chr12:123589795-123590608	ECC-1	luminal epithelium:	n/a	n/a
11	NFIC	chr12:123589818-123590557	ECC-1	luminal epithelium:	n/a	n/a
12	JUND	chr12:123590083-123590444	HepG2	liver:	n/a	chr12:123590111-123590120
13	EP300	chr12:123589826-123590471	ECC-1	luminal epithelium:	n/a	chr12:123590108-123590122 chr12:123590085-123590098 chr12:123590369-123590383
14	TCF12	chr12:123589675-123590717	ECC-1	luminal epithelium:	n/a	chr12:123590157-123590164
15	GABPA	chr12:123590003-123590221	Hela-S3	cervix:	n/a	n/a
16	JUN	chr12:123589953-123590431	HUVEC	blood vessel:	n/a	chr12:123590257-123590270 chr12:123590111-123590120
17	POLR2A	chr12:123589913-123590186	Hela-S3	cervix:	n/a	n/a
18	TEAD4	chr12:123589787-123590528	ECC-1	luminal epithelium:	n/a	n/a
19	JUND	chr12:123590098-123590391	H1-hESC	embryonic stem cell:	n/a	chr12:123590111-123590120
20	MAX	chr12:123589839-123590666	ECC-1	luminal epithelium:	n/a	n/a
21	STAT3	chr12:123589946-123590386	MCF10A-Er-Src	breast:	n/a	n/a
22	TEAD4	chr12:123589802-123590413	ECC-1	luminal epithelium:	n/a	n/a
23	JUN	chr12:123590129-123590397	HepG2	liver:	n/a	chr12:123590257-123590270
24	FOS	chr12:123590015-123590377	MCF10A-Er-Src	breast:	n/a	chr12:123590111-123590120
25	CREB1	chr12:123589948-123590510	ECC-1	luminal epithelium:	n/a	n/a
26	CREB1	chr12:123590037-123590349	H1-hESC	embryonic stem cell:	n/a	n/a
27	POLR2A	chr12:123589865-123590315	ECC-1	luminal epithelium:	n/a	n/a
28	STAT3	chr12:123589963-123590356	MCF10A-Er-Src	breast:	n/a	n/a
29	JUN	chr12:123590146-123590367	H1-hESC	embryonic stem cell:	n/a	chr12:123590257-123590270
30	EP300	chr12:123589743-123590706	ECC-1	luminal epithelium:	n/a	chr12:123590108-123590122 chr12:123590085-123590098 chr12:123590369-123590383
31	KAP1	chr12:123589961-123590373	HEK293	kidney:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:123588003..123590511-chr12:123634129..123636612,2	MCF-7	breast:
2	chr12:123589646..123591494-chr12:123593029..123596172,4	K562	blood:
3	chr12:123500117..123502770-chr12:123590126..123592827,2	K562	blood:

Variant related genes	Relation type
PITPNM2	TF binding region
ENSG00000265603	Chromatin interaction
ENSG00000090975	Chromatin interaction

Extended variants
information (count: 141 )
Associated
traits (count: 14 )

rSNPs within LD-proxies of this variant (count:135)

rs_ID	r²[population]
rs1047158	0.91[EUR][1000 genomes]
rs1051431	0.94[CEU][hapmap];0.97[TSI][hapmap];0.89[EUR][1000 genomes]
rs10744147	0.85[EUR][1000 genomes]
rs10772993	0.86[EUR][1000 genomes]
rs10772995	0.85[EUR][1000 genomes]
rs10772998	0.89[CEU][hapmap]
rs10846478	0.85[EUR][1000 genomes]
rs10846486	0.94[CEU][hapmap];0.82[EUR][1000 genomes]
rs11057192	0.89[CEU][hapmap];0.97[TSI][hapmap];0.86[EUR][1000 genomes]
rs1106240	0.94[CEU][hapmap];0.82[GIH][hapmap];0.94[TSI][hapmap];0.88[EUR][1000 genomes]
rs1106241	0.94[CEU][hapmap];0.82[GIH][hapmap];0.97[TSI][hapmap];0.90[EUR][1000 genomes]
rs1260294	1.00[CEU][hapmap];0.87[GIH][hapmap];0.97[TSI][hapmap];0.93[EUR][1000 genomes]
rs12817892	0.91[CEU][hapmap]
rs12820906	1.00[CHB][hapmap];0.90[JPT][hapmap];0.82[ASN][1000 genomes]
rs1402274	0.94[CEU][hapmap];0.84[GIH][hapmap];0.97[TSI][hapmap];0.87[EUR][1000 genomes]
rs1463877	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.84[ASN][1000 genomes]
rs1533703	0.88[CEU][hapmap]
rs1569068	0.94[CEU][hapmap];0.97[TSI][hapmap];0.89[EUR][1000 genomes]
rs1615350	0.84[CEU][hapmap];0.82[TSI][hapmap]
rs1615694	0.84[EUR][1000 genomes]
rs1616131	0.92[EUR][1000 genomes]
rs1616181	0.92[EUR][1000 genomes]
rs1617434	0.87[EUR][1000 genomes]
rs1618679	0.86[EUR][1000 genomes]
rs1621194	0.89[EUR][1000 genomes]
rs1626899	0.84[EUR][1000 genomes]
rs1627724	0.91[EUR][1000 genomes]
rs1630693	0.84[EUR][1000 genomes]
rs1630905	0.85[EUR][1000 genomes]
rs1716156	0.81[EUR][1000 genomes]
rs1716157	0.94[CEU][hapmap];0.81[GIH][hapmap];0.97[TSI][hapmap];0.85[EUR][1000 genomes]
rs1716159	0.85[EUR][1000 genomes]
rs1716160	0.94[CEU][hapmap];0.97[TSI][hapmap];0.86[EUR][1000 genomes]
rs1716164	0.94[CEU][hapmap];0.81[GIH][hapmap];0.97[TSI][hapmap];0.83[EUR][1000 genomes]
rs1716165	0.94[CEU][hapmap];0.97[TSI][hapmap];0.89[EUR][1000 genomes]
rs1716167	0.94[CEU][hapmap];0.82[GIH][hapmap];0.97[TSI][hapmap];0.89[EUR][1000 genomes]
rs1716168	0.94[CEU][hapmap];0.82[GIH][hapmap];0.97[TSI][hapmap];0.89[EUR][1000 genomes]
rs1716170	0.94[CEU][hapmap];0.94[TSI][hapmap]
rs1716171	0.94[CEU][hapmap];0.94[TSI][hapmap]
rs1716172	0.81[EUR][1000 genomes]
rs1716173	0.83[EUR][1000 genomes]
rs1716175	0.94[CEU][hapmap];0.85[EUR][1000 genomes]
rs1716176	0.94[CEU][hapmap];0.88[EUR][1000 genomes]
rs1716177	0.94[CEU][hapmap];0.88[EUR][1000 genomes]
rs1716182	0.84[EUR][1000 genomes]
rs1716185	0.88[EUR][1000 genomes]
rs1727290	0.88[EUR][1000 genomes]
rs1727294	0.93[CEU][hapmap];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1727296	0.94[CEU][hapmap];0.89[EUR][1000 genomes]
rs1727300	0.83[EUR][1000 genomes]
rs1727302	0.84[CEU][hapmap];0.81[GIH][hapmap];0.82[TSI][hapmap]
rs1727306	0.94[CEU][hapmap];0.85[EUR][1000 genomes]
rs1727307	0.85[YRI][hapmap]
rs1727309	0.94[CEU][hapmap];0.81[GIH][hapmap];0.91[TSI][hapmap];0.83[EUR][1000 genomes]
rs1727310	0.83[EUR][1000 genomes]
rs1727313	0.94[CEU][hapmap];0.94[TSI][hapmap];0.87[EUR][1000 genomes]
rs1727314	0.89[EUR][1000 genomes]
rs1727315	0.94[CEU][hapmap];0.97[TSI][hapmap];0.91[EUR][1000 genomes]
rs1727316	0.92[EUR][1000 genomes]
rs1727317	0.89[EUR][1000 genomes]
rs1727318	0.85[EUR][1000 genomes]
rs1727320	0.94[CEU][hapmap];0.86[EUR][1000 genomes]
rs1727323	0.94[CEU][hapmap];0.97[TSI][hapmap];0.86[EUR][1000 genomes]
rs1727324	0.94[CEU][hapmap];0.83[EUR][1000 genomes]
rs1727325	0.94[CEU][hapmap];0.86[EUR][1000 genomes]
rs1727334	0.86[CEU][hapmap]
rs1790086	0.85[EUR][1000 genomes]
rs1790087	0.85[EUR][1000 genomes]
rs1790089	0.87[EUR][1000 genomes]
rs1790090	0.91[EUR][1000 genomes]
rs1790095	0.94[CEU][hapmap];0.81[GIH][hapmap];0.97[TSI][hapmap];0.87[EUR][1000 genomes]
rs1790098	0.94[CEU][hapmap];0.81[GIH][hapmap];0.97[TSI][hapmap];0.88[EUR][1000 genomes]
rs1790100	0.94[CEU][hapmap];0.87[EUR][1000 genomes]
rs1790101	0.84[EUR][1000 genomes]
rs1790102	0.84[EUR][1000 genomes]
rs1790108	0.94[CEU][hapmap];0.82[GIH][hapmap];0.97[TSI][hapmap];0.91[EUR][1000 genomes]
rs1790109	0.91[EUR][1000 genomes]
rs1790116	0.88[CEU][hapmap];0.82[GIH][hapmap];0.97[TSI][hapmap];0.92[EUR][1000 genomes]
rs1790119	0.85[ASN][1000 genomes]
rs1790120	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1790123	0.94[CEU][hapmap];0.81[GIH][hapmap];0.94[TSI][hapmap];0.83[EUR][1000 genomes]
rs1790124	0.82[EUR][1000 genomes]
rs1790130	0.84[EUR][1000 genomes]
rs1790131	0.94[CEU][hapmap];0.97[TSI][hapmap];0.85[EUR][1000 genomes]
rs1879380	0.94[CEU][hapmap];0.88[TSI][hapmap]
rs1969354	0.89[CEU][hapmap];0.91[TSI][hapmap]
rs1980252	0.89[CEU][hapmap]
rs2049114	0.94[CEU][hapmap];0.85[EUR][1000 genomes]
rs2270789	1.00[CHB][hapmap];0.94[CHD][hapmap];0.89[JPT][hapmap];0.93[ASN][1000 genomes]
rs2337934	0.89[CEU][hapmap];0.94[TSI][hapmap]
rs2510885	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2682429	0.91[EUR][1000 genomes]
rs2682430	0.84[EUR][1000 genomes]
rs2682431	0.86[EUR][1000 genomes]
rs2682433	0.84[EUR][1000 genomes]
rs2682434	0.94[CEU][hapmap];0.97[TSI][hapmap];0.86[EUR][1000 genomes]
rs2695476	0.84[EUR][1000 genomes]
rs2695478	0.94[CEU][hapmap];0.81[GIH][hapmap];0.94[TSI][hapmap];0.85[EUR][1000 genomes]
rs2695479	0.83[EUR][1000 genomes]
rs2695480	0.82[EUR][1000 genomes]
rs2695481	0.91[EUR][1000 genomes]
rs2695482	0.94[CEU][hapmap];0.90[EUR][1000 genomes]
rs2851435	0.81[EUR][1000 genomes]
rs2851436	0.83[EUR][1000 genomes]
rs2851438	0.91[EUR][1000 genomes]
rs2851441	0.85[EUR][1000 genomes]
rs2851447	0.82[CEU][hapmap]
rs2851450	0.86[EUR][1000 genomes]
rs2851451	0.85[EUR][1000 genomes]
rs2947099	0.84[EUR][1000 genomes]
rs2950537	0.84[EUR][1000 genomes]
rs3018098	0.88[EUR][1000 genomes]
rs4372492	0.94[CEU][hapmap];0.86[EUR][1000 genomes]
rs4460848	0.84[CEU][hapmap];0.84[TSI][hapmap]
rs4759371	0.89[CEU][hapmap];0.94[TSI][hapmap]
rs4759409	0.89[CEU][hapmap]
rs4759415	0.89[CEU][hapmap];0.94[TSI][hapmap]
rs520088	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.84[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs585522	1.00[ASW][hapmap];0.84[CEU][hapmap];0.94[CHB][hapmap];0.89[CHD][hapmap];0.90[JPT][hapmap];1.00[LWK][hapmap];0.85[MKK][hapmap];0.92[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs641760	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs655293	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];0.88[LWK][hapmap];1.00[MEX][hapmap];0.80[MKK][hapmap];1.00[TSI][hapmap];0.88[YRI][hapmap];0.85[AFR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7132277	0.94[CEU][hapmap];0.81[GIH][hapmap];0.88[TSI][hapmap];0.85[EUR][1000 genomes]
rs71444568	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7296418	0.81[MEX][hapmap];0.87[YRI][hapmap]
rs7299943	0.93[ASW][hapmap];0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.91[TSI][hapmap];0.92[YRI][hapmap];0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7313483	0.89[CEU][hapmap]
rs7953929	0.94[CEU][hapmap]
rs7975763	0.92[AFR][1000 genomes];0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs883263	1.00[ASW][hapmap];0.94[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.97[GIH][hapmap];0.90[JPT][hapmap];0.85[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.88[YRI][hapmap];0.84[ASN][1000 genomes]
rs884548	0.94[CEU][hapmap];0.91[EUR][1000 genomes]
rs937564	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.94[GIH][hapmap];0.90[JPT][hapmap];1.00[MEX][hapmap];0.82[MKK][hapmap];1.00[TSI][hapmap];0.88[YRI][hapmap];0.81[ASN][1000 genomes]
rs940904	0.93[ASW][hapmap];0.83[CHB][hapmap];0.81[JPT][hapmap];0.82[LWK][hapmap];0.92[YRI][hapmap]
rs941305	0.94[CEU][hapmap]
rs941306	0.94[CEU][hapmap]
rs949142	0.91[EUR][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	esv3388790	chr12:123275902-123655103	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
2	nsv517200	chr12:123312051-123654498	Strong transcription Weak transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
3	nsv427924	chr12:123412172-123722059	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	78 gene(s)	inside rSNPs	diseases
4	nsv1042550	chr12:123532028-123659500	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
5	esv1825473	chr12:123582855-123822503	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
6	nsv870326	chr12:123585990-123719323	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases

mRNA abundance (count:14)

SNP	Gene	Cis/trans	Tissue	Source
rs1617156	CDK2AP1	cis	lymphoblastoid	seeQTL
rs1617156	SBNO1	Cis_1M	lymphoblastoid	RTeQTL
rs1617156	MPHOSPH9	cis	Esophagus Muscularis	GTEx
rs1617156	TMEM120B	cis	parietal	SCAN
rs1617156	ARL6IP4	Cis_1M	lymphoblastoid	RTeQTL
rs1617156	RP11-282O18.3	cis	Esophagus Mucosa	GTEx
rs1617156	CCDC92	cis	cerebellum	SCAN
rs1617156	PITPNM2	cis	cerebellum	SCAN
rs1617156	CDK2AP1	Cis_1M	lymphoblastoid	RTeQTL
rs1617156	MPHOSPH9	Cis_1M	lymphoblastoid	RTeQTL
rs1617156	HIP1R	cis	parietal	SCAN
rs1617156	CDK2AP1	cis	Esophagus Mucosa	GTEx
rs1617156	ANAPC5	cis	parietal	SCAN
rs1617156	LOC283378	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:123561600-123604000	Genic enhancers	Fetal Thymus	thymus
2	chr12:123571200-123600000	Genic enhancers	Thymus	Thymus
3	chr12:123577000-123590400	Weak transcription	Primary hematopoietic stem cells	blood
4	chr12:123577400-123590200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr12:123579800-123593600	Weak transcription	Fetal Intestine Large	intestine
6	chr12:123579800-123596200	Weak transcription	Osteobl	bone
7	chr12:123580000-123592600	Weak transcription	NHEK	skin
8	chr12:123580000-123593800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr12:123580200-123590200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr12:123580200-123593200	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr12:123580600-123596000	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr12:123581000-123593000	Weak transcription	Pancreas	Pancrea
13	chr12:123581200-123593000	Weak transcription	Brain Germinal Matrix	brain
14	chr12:123581400-123591600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr12:123582200-123591200	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr12:123582600-123591200	Weak transcription	Brain Hippocampus Middle	brain
17	chr12:123582800-123591200	Weak transcription	Duodenum Mucosa	Duodenum
18	chr12:123582800-123591400	Weak transcription	Brain Substantia Nigra	brain
19	chr12:123582800-123592600	Weak transcription	Gastric	stomach
20	chr12:123583000-123591200	Weak transcription	Rectal Smooth Muscle	rectum
21	chr12:123583000-123591400	Weak transcription	HSMM	muscle
22	chr12:123583000-123595800	Weak transcription	NHDF-Ad	bronchial
23	chr12:123583200-123599600	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr12:123583600-123591800	Weak transcription	HSMMtube	muscle
25	chr12:123583600-123592000	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr12:123584600-123593400	Weak transcription	Colonic Mucosa	Colon
27	chr12:123584800-123590200	Weak transcription	Primary B cells from peripheral blood	blood
28	chr12:123584800-123591800	Weak transcription	Colon Smooth Muscle	Colon
29	chr12:123585400-123590400	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr12:123585800-123590400	Weak transcription	Brain Angular Gyrus	brain
31	chr12:123586000-123592600	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr12:123586200-123590200	Weak transcription	Fetal Brain Female	brain
33	chr12:123586400-123590200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr12:123586400-123590200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
35	chr12:123586600-123591200	Strong transcription	Cortex derived primary cultured neurospheres	brain
36	chr12:123586600-123591200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr12:123586800-123592200	Enhancers	HepG2	liver
38	chr12:123587200-123590400	Weak transcription	Brain Cingulate Gyrus	brain
39	chr12:123587200-123591600	Enhancers	Primary T cells from cord blood	blood
40	chr12:123587200-123595600	Enhancers	Liver	Liver
41	chr12:123587400-123590200	Weak transcription	Fetal Muscle Leg	muscle
42	chr12:123587400-123591000	Weak transcription	Brain Anterior Caudate	brain
43	chr12:123587400-123591400	Weak transcription	H9 Cell Line	embryonic stem cell
44	chr12:123587800-123591000	Weak transcription	K562	blood
45	chr12:123588000-123590400	Weak transcription	Primary B cells from cord blood	blood
46	chr12:123588000-123599000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr12:123588200-123590200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
48	chr12:123588200-123591200	Weak transcription	Esophagus	oesophagus
49	chr12:123588200-123591200	Weak transcription	A549	lung
50	chr12:123588200-123591400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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