Variant report

Variant	rs812383
Chromosome Location	chr2:233737132-233737133
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:47)
CpG islands
(count:0)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:47 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr2:233734109-233737469	HepG2	liver:	n/a	n/a
2	MAZ	chr2:233736640-233737272	HepG2	liver:	n/a	n/a
3	RAD21	chr2:233737077-233737247	HepG2	liver:	n/a	n/a
4	POLR2A	chr2:233736642-233737408	HepG2	liver:	n/a	n/a
5	RAD21	chr2:233736790-233737179	HepG2	liver:	n/a	n/a
6	FOXA1	chr2:233736590-233737433	HepG2	liver:	n/a	n/a
7	ZBTB7A	chr2:233736582-233737186	HepG2	liver:	n/a	n/a
8	POLR2A	chr2:233735472-233738418	A549	lung:	n/a	n/a
9	MBD4	chr2:233736166-233737976	HepG2	liver:	n/a	n/a
10	POLR2A	chr2:233735959-233739644	HepG2	liver:	n/a	n/a
11	MBD4	chr2:233736602-233737350	HepG2	liver:	n/a	n/a
12	HEY1	chr2:233736501-233737464	HepG2	liver:	n/a	n/a
13	POLR2A	chr2:233733915-233737373	HepG2	liver:	n/a	n/a
14	CEBPD	chr2:233736584-233737224	HepG2	liver:	n/a	n/a
15	MYC	chr2:233736866-233737198	HepG2	liver:	n/a	n/a
16	EP300	chr2:233736694-233737447	HepG2	liver:	n/a	n/a
17	NFIC	chr2:233736022-233737445	HepG2	liver:	n/a	n/a
18	NFIC	chr2:233736659-233737355	HepG2	liver:	n/a	n/a
19	SMC3	chr2:233736961-233737150	HepG2	liver:	n/a	n/a
20	MYBL2	chr2:233735996-233737757	HepG2	liver:	n/a	n/a
21	FOXA1	chr2:233736689-233737322	HepG2	liver:	n/a	n/a
22	RCOR1	chr2:233736792-233737255	HepG2	liver:	n/a	n/a
23	TBP	chr2:233736760-233737239	HepG2	liver:	n/a	n/a
24	MAX	chr2:233736853-233737358	HepG2	liver:	n/a	n/a
25	POLR2A	chr2:233736322-233737490	ECC-1	luminal epithelium:	n/a	n/a
26	POLR2A	chr2:233737097-233737443	HepG2	liver:	n/a	n/a
27	EP300	chr2:233736709-233737299	HepG2	liver:	n/a	n/a
28	MAFK	chr2:233737007-233737262	HepG2	liver:	n/a	n/a
29	HNF4A	chr2:233736765-233737295	HepG2	liver:	n/a	chr2:233736836-233736843 chr2:233736832-233736848
30	EP300	chr2:233736512-233737313	HepG2	liver:	n/a	n/a
31	TEAD4	chr2:233736607-233737415	HepG2	liver:	n/a	n/a
32	POLR2A	chr2:233735463-233740850	HepG2	liver:	n/a	n/a
33	FOXA1	chr2:233736619-233737380	HepG2	liver:	n/a	n/a
34	FOXA1	chr2:233736669-233737383	HepG2	liver:	n/a	n/a
35	REST	chr2:233736792-233737223	HepG2	liver:	n/a	chr2:233737013-233737026
36	POLR2A	chr2:233736214-233737470	HepG2	liver:	n/a	n/a
37	YY1	chr2:233736224-233737428	HepG2	liver:	n/a	n/a
38	CHD2	chr2:233736728-233737454	HepG2	liver:	n/a	n/a
39	FOXA2	chr2:233736696-233737288	HepG2	liver:	n/a	n/a
40	HDAC2	chr2:233736639-233737373	HepG2	liver:	n/a	n/a
41	MYBL2	chr2:233736583-233737589	HepG2	liver:	n/a	n/a
42	SP1	chr2:233736675-233737362	HepG2	liver:	n/a	chr2:233736720-233736734 chr2:233737324-233737338 chr2:233736839-233736849
43	POLR2A	chr2:233734116-233737517	HepG2	liver:	n/a	n/a
44	CEBPB	chr2:233737057-233737174	HepG2	liver:	n/a	n/a
45	HEY1	chr2:233735984-233737336	HepG2	liver:	n/a	n/a
46	HDAC2	chr2:233736649-233737308	HepG2	liver:	n/a	n/a
47	TAF1	chr2:233736144-233737447	HepG2	liver:	n/a	n/a

No data

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:233723605..233727098-chr2:233736700..233739372,3	MCF-7	breast:
2	chr2:233730563..233732599-chr2:233735089..233737149,2	K562	blood:
3	chr2:233736761..233738349-chr2:233835083..233836654,2	MCF-7	breast:
4	chr2:233735745..233738389-chr2:234136756..234138303,2	MCF-7	breast:

No data

Variant related genes	Relation type
C2orf82	TF binding region

Extended variants
information (count: 95 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:86)

rs_ID	r²[population]
rs1022330	0.85[CHB][hapmap];0.85[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap]
rs10933411	0.96[ASN][1000 genomes]
rs10933412	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs11555646	1.00[CHB][hapmap];0.90[CHD][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.86[MKK][hapmap]
rs11676216	0.94[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs11679079	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap]
rs12474040	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12694917	0.96[ASN][1000 genomes]
rs12990821	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13003675	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13004406	0.85[CHB][hapmap];0.85[CHD][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.86[MKK][hapmap]
rs13011298	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13013142	1.00[CHB][hapmap];0.90[CHD][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.86[MKK][hapmap]
rs1446308	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs1446310	0.85[ASN][1000 genomes]
rs1446311	1.00[CHB][hapmap];1.00[CHD][hapmap];0.87[GIH][hapmap];0.90[JPT][hapmap];0.84[MEX][hapmap];0.92[MKK][hapmap];0.95[ASN][1000 genomes]
rs1801251	1.00[CHB][hapmap];0.90[CHD][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.90[MKK][hapmap]
rs1867778	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs1947105	1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.92[MKK][hapmap];0.98[ASN][1000 genomes]
rs2012221	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs2044449	0.98[ASN][1000 genomes]
rs2100053	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2166441	0.89[LWK][hapmap];0.87[MKK][hapmap];0.91[YRI][hapmap]
rs2197563	0.93[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap]
rs2250654	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2250665	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2305137	0.96[ASN][1000 genomes]
rs2305141	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs2592102	0.98[ASN][1000 genomes]
rs2592113	0.85[ASN][1000 genomes]
rs2592115	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2592116	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2592117	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2592126	0.96[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2674839	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs2675957	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2675966	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2675967	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.94[MKK][hapmap];1.00[TSI][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2675971	0.94[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2675973	0.96[ASN][1000 genomes]
rs2675974	1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs283466	0.85[ASN][1000 genomes]
rs283468	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.84[ASN][1000 genomes]
rs283469	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs283471	1.00[CHB][hapmap];0.93[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs283474	1.00[CHB][hapmap];0.93[CHD][hapmap];0.89[GIH][hapmap];0.95[JPT][hapmap];0.82[ASN][1000 genomes]
rs283475	1.00[CHB][hapmap];0.97[CHD][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs283476	1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs283486	1.00[CHB][hapmap];0.90[CHD][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.90[MKK][hapmap]
rs3816334	0.96[ASN][1000 genomes]
rs3817311	1.00[CHB][hapmap];0.88[CHD][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap];0.89[MKK][hapmap]
rs4973053	0.85[ASN][1000 genomes]
rs4973054	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs4973055	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs4973056	0.95[ASN][1000 genomes]
rs4973560	0.83[ASN][1000 genomes]
rs4973561	0.85[ASN][1000 genomes]
rs6437074	1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.92[MKK][hapmap];0.96[ASN][1000 genomes]
rs6704768	0.81[JPT][hapmap]
rs6714245	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs6717841	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6719061	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs6738386	1.00[CHB][hapmap];0.90[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap]
rs6745879	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6746294	1.00[CHB][hapmap];0.95[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap]
rs6747645	0.84[GIH][hapmap];0.85[JPT][hapmap]
rs6748027	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs709933	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.90[MKK][hapmap];1.00[TSI][hapmap];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs709934	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs709938	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs737028	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7558609	1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.92[MKK][hapmap];0.87[ASN][1000 genomes]
rs7568385	0.81[ASN][1000 genomes]
rs7573208	0.87[ASN][1000 genomes]
rs7587309	0.95[ASN][1000 genomes]
rs7589201	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs7606090	1.00[CHB][hapmap];0.90[CHD][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap]
rs778166	0.80[ASN][1000 genomes]
rs778338	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs778339	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs778340	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.81[MKK][hapmap];1.00[TSI][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs778368	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs809639	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs895430	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs9653383	0.84[ASN][1000 genomes]
rs991873	0.95[CHB][hapmap];0.97[CHD][hapmap];0.92[GIH][hapmap];0.95[JPT][hapmap];0.85[MEX][hapmap];0.92[MKK][hapmap];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948470	chr2:233166262-233886732	Enhancers Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
2	nsv1005123	chr2:233227729-233920152	Enhancers Strong transcription Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
3	nsv536173	chr2:233227729-233920152	Bivalent Enhancer Strong transcription Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
4	nsv834570	chr2:233639160-233805067	Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv1009825	chr2:233709566-233763470	Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv984452	chr2:233725452-233762965	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	nsv999116	chr2:233733352-233759864	Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	nsv1007029	chr2:233733352-233760519	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
9	nsv536179	chr2:233735380-233757170	Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs812383	C2orf82	cis	Frontal Cortex	GTEx
rs812383	HMGB3L1	trans	parietal	SCAN
rs812383	C2orf82	cis	Temporal Cortex	GTEx
rs812383	C2orf82	cis	parietal	SCAN
rs812383	C2orf82	cis	Skin Sun Exposed Lower leg	GTEx

Chromatin state (count:59 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:233722800-233738000	Weak transcription	Stomach Mucosa	stomach
2	chr2:233723000-233740400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr2:233723200-233738600	Weak transcription	K562	blood
4	chr2:233724200-233738600	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr2:233724600-233738600	Weak transcription	Esophagus	oesophagus
6	chr2:233726000-233737400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr2:233726000-233740400	Weak transcription	HMEC	breast
8	chr2:233726200-233737400	Weak transcription	Fetal Brain Female	brain
9	chr2:233726400-233738200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr2:233726400-233739000	Weak transcription	Thymus	Thymus
11	chr2:233726400-233740200	Weak transcription	Primary B cells from cord blood	blood
12	chr2:233726400-233740400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr2:233726400-233740800	Weak transcription	HSMM	muscle
14	chr2:233726600-233737800	Weak transcription	Brain Germinal Matrix	brain
15	chr2:233726600-233738200	Weak transcription	Gastric	stomach
16	chr2:233726600-233738400	Weak transcription	Primary monocytes fromperipheralblood	blood
17	chr2:233726600-233738400	Weak transcription	Placenta	Placenta
18	chr2:233726600-233738800	Weak transcription	NHLF	lung
19	chr2:233726600-233739000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr2:233726600-233739200	Weak transcription	Left Ventricle	heart
21	chr2:233726600-233739800	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr2:233726600-233740000	Weak transcription	Pancreas	Pancrea
23	chr2:233726600-233740200	Weak transcription	Rectal Smooth Muscle	rectum
24	chr2:233726600-233740400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr2:233726600-233740400	Weak transcription	Lung	lung
26	chr2:233726600-233740400	Weak transcription	NHEK	skin
27	chr2:233726800-233755600	Weak transcription	HSMMtube	muscle
28	chr2:233727800-233738400	Weak transcription	Monocytes-CD14+_RO01746	blood
29	chr2:233727800-233738600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr2:233732600-233738200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr2:233734000-233737200	Enhancers	Brain Anterior Caudate	brain
32	chr2:233734200-233739600	Flanking Active TSS	HepG2	liver
33	chr2:233734400-233737800	Weak transcription	Duodenum Mucosa	Duodenum
34	chr2:233734400-233740400	Enhancers	Brain Inferior Temporal Lobe	brain
35	chr2:233734600-233740200	Enhancers	Brain Cingulate Gyrus	brain
36	chr2:233734600-233740200	Enhancers	Brain Substantia Nigra	brain
37	chr2:233734800-233740200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr2:233735000-233739200	Enhancers	Brain Angular Gyrus	brain
39	chr2:233735000-233740000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
40	chr2:233735000-233740000	Genic enhancers	Fetal Intestine Small	intestine
41	chr2:233735200-233738600	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr2:233735200-233738600	Weak transcription	Spleen	Spleen
43	chr2:233735600-233738200	Weak transcription	Liver	Liver
44	chr2:233735800-233737200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr2:233736000-233737800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr2:233736200-233738000	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr2:233736200-233738000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr2:233736400-233740200	Enhancers	Fetal Intestine Large	intestine
49	chr2:233736600-233737400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr2:233736600-233737400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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