Variant report

Variant	rs2592117
Chromosome Location	chr2:233735693-233735694
allele	A/G
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	HNF4G	chr2:233735578-233735970	HepG2	liver:	n/a	chr2:233735774-233735782 chr2:233735796-233735814 chr2:233735826-233735840 chr2:233735650-233735663 chr2:233735827-233735839 chr2:233735827-233735840 chr2:233735650-233735663 chr2:233735827-233735839 chr2:233735654-233735662 chr2:233735770-233735784 chr2:233735798-233735813
2	POLR2A	chr2:233734109-233737469	HepG2	liver:	n/a	n/a
3	POLR2A	chr2:233735623-233735937	HepG2	liver:	n/a	n/a
4	POLR2A	chr2:233735668-233735802	K562	blood:	n/a	n/a
5	HNF4A	chr2:233735505-233735946	HepG2	liver:	n/a	chr2:233735797-233735812 chr2:233735774-233735782 chr2:233735796-233735814 chr2:233735826-233735840 chr2:233735650-233735663 chr2:233735827-233735839 chr2:233735827-233735840 chr2:233735650-233735663 chr2:233735827-233735839 chr2:233735654-233735662 chr2:233735770-233735784
6	POLR2A	chr2:233735472-233738418	A549	lung:	n/a	n/a
7	POLR2A	chr2:233735522-233735722	HepG2	liver:	n/a	n/a
8	POLR2A	chr2:233733915-233737373	HepG2	liver:	n/a	n/a
9	CHD2	chr2:233735665-233735729	HepG2	liver:	n/a	n/a
10	HNF4A	chr2:233735621-233735954	HepG2	liver:	n/a	chr2:233735797-233735812 chr2:233735774-233735782 chr2:233735796-233735814 chr2:233735826-233735840 chr2:233735650-233735663 chr2:233735827-233735839 chr2:233735827-233735840 chr2:233735650-233735663 chr2:233735827-233735839 chr2:233735654-233735662 chr2:233735770-233735784
11	HEY1	chr2:233735514-233735978	HepG2	liver:	n/a	n/a
12	POLR2A	chr2:233735463-233740850	HepG2	liver:	n/a	n/a
13	POLR2A	chr2:233735575-233736186	HepG2	liver:	n/a	n/a
14	POLR2A	chr2:233734116-233737517	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:233730563..233732599-chr2:233735089..233737149,2	K562	blood:
2	chr2:233733606..233736774-chr2:233738541..233741120,3	K562	blood:
3	chr2:233733606..233736578-chr2:233738541..233742093,3	K562	blood:

Variant related genes	Relation type
C2orf82	TF binding region
ENSG00000182600	Chromatin interaction

Extended variants
information (count: 94 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:85)

rs_ID	r²[population]
rs1022330	0.83[ASW][hapmap];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];0.96[ASN][1000 genomes]
rs11555646	1.00[CHB][hapmap];0.90[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap]
rs11676216	0.94[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs11679079	1.00[CHB][hapmap];1.00[JPT][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];0.92[GIH][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap];0.83[YRI][hapmap]
rs13011298	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap]
rs13013142	1.00[CHB][hapmap];0.90[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap]
rs1446308	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1446310	0.85[ASN][1000 genomes]
rs1446311	1.00[CHB][hapmap];1.00[CHD][hapmap];0.90[GIH][hapmap];0.90[JPT][hapmap];0.81[MEX][hapmap];0.95[ASN][1000 genomes]
rs1801251	1.00[CHB][hapmap];0.90[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap]
rs1867778	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs1947105	1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap];0.98[ASN][1000 genomes]
rs2012221	0.85[CHB][hapmap];1.00[JPT][hapmap]
rs2044449	0.84[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs2100053	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2197563	0.88[ASW][hapmap];0.93[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap]
rs2250654	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2250665	0.95[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[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2592116	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[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];0.94[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	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2675966	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2675967	0.83[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.82[LWK][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.98[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	0.88[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.96[ASN][1000 genomes]
rs283466	0.85[ASN][1000 genomes]
rs283468	1.00[CHB][hapmap];1.00[JPT][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];0.95[GIH][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs283474	1.00[CHB][hapmap];0.93[CHD][hapmap];0.92[GIH][hapmap];0.95[JPT][hapmap];0.92[LWK][hapmap];0.81[MEX][hapmap];0.91[YRI][hapmap];0.82[ASN][1000 genomes]
rs283475	0.82[ASW][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs283476	1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.81[ASN][1000 genomes]
rs283486	1.00[CHB][hapmap];0.90[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap]
rs3816334	0.96[ASN][1000 genomes]
rs3817311	1.00[CHB][hapmap];0.88[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap]
rs4973053	0.85[ASN][1000 genomes]
rs4973054	1.00[CHB][hapmap];1.00[JPT][hapmap];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];0.95[GIH][hapmap];1.00[JPT][hapmap];0.81[MEX][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	0.83[ASW][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.81[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];0.81[MEX][hapmap]
rs6747645	0.84[GIH][hapmap];0.85[JPT][hapmap]
rs6748027	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs709933	0.83[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs709934	0.83[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs709938	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs737028	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap]
rs7558609	1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap];0.87[ASN][1000 genomes]
rs7568385	0.81[ASN][1000 genomes]
rs7573208	0.87[ASN][1000 genomes]
rs7587309	0.82[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs7589201	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs7606090	0.83[ASW][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap]
rs778166	0.80[ASN][1000 genomes]
rs778338	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs778339	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs778340	0.88[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];0.90[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs778368	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs809639	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];1.00[MEX][hapmap];0.89[MKK][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap];0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs812383	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]
rs895430	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.87[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs9653383	0.84[ASN][1000 genomes]
rs991873	0.95[CHB][hapmap];0.97[CHD][hapmap];0.95[GIH][hapmap];0.95[JPT][hapmap];0.81[MEX][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:3)

SNP	Gene	Cis/trans	Tissue	Source
rs2592117	HMGB3L1	trans	parietal	SCAN
rs2592117	C2orf82	cis	parietal	SCAN
rs2592117	C2orf82	cis	Skin Sun Exposed Lower leg	GTEx

Chromatin state (count:68 , 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	chr2:233723200-233736600	Weak transcription	Colonic Mucosa	Colon
4	chr2:233723200-233738600	Weak transcription	K562	blood
5	chr2:233723600-233736400	Weak transcription	Right Ventricle	heart
6	chr2:233723600-233736600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr2:233724000-233736000	Weak transcription	Fetal Brain Male	brain
8	chr2:233724200-233738600	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr2:233724600-233738600	Weak transcription	Esophagus	oesophagus
10	chr2:233725000-233735800	Weak transcription	Fetal Thymus	thymus
11	chr2:233726000-233737400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr2:233726000-233740400	Weak transcription	HMEC	breast
13	chr2:233726200-233737400	Weak transcription	Fetal Brain Female	brain
14	chr2:233726400-233736000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr2:233726400-233736200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr2:233726400-233736200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr2:233726400-233738200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr2:233726400-233739000	Weak transcription	Thymus	Thymus
19	chr2:233726400-233740200	Weak transcription	Primary B cells from cord blood	blood
20	chr2:233726400-233740400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr2:233726400-233740800	Weak transcription	HSMM	muscle
22	chr2:233726600-233735800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr2:233726600-233736000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr2:233726600-233736200	Weak transcription	Primary hematopoietic stem cells	blood
25	chr2:233726600-233737800	Weak transcription	Brain Germinal Matrix	brain
26	chr2:233726600-233738200	Weak transcription	Gastric	stomach
27	chr2:233726600-233738400	Weak transcription	Primary monocytes fromperipheralblood	blood
28	chr2:233726600-233738400	Weak transcription	Placenta	Placenta
29	chr2:233726600-233738800	Weak transcription	NHLF	lung
30	chr2:233726600-233739000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr2:233726600-233739200	Weak transcription	Left Ventricle	heart
32	chr2:233726600-233739800	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr2:233726600-233740000	Weak transcription	Pancreas	Pancrea
34	chr2:233726600-233740200	Weak transcription	Rectal Smooth Muscle	rectum
35	chr2:233726600-233740400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr2:233726600-233740400	Weak transcription	Lung	lung
37	chr2:233726600-233740400	Weak transcription	NHEK	skin
38	chr2:233726800-233736400	Weak transcription	Fetal Intestine Large	intestine
39	chr2:233726800-233736600	Weak transcription	Stomach Smooth Muscle	stomach
40	chr2:233726800-233755600	Weak transcription	HSMMtube	muscle
41	chr2:233727800-233736000	Weak transcription	A549	lung
42	chr2:233727800-233736200	Weak transcription	Cortex derived primary cultured neurospheres	brain
43	chr2:233727800-233738400	Weak transcription	Monocytes-CD14+_RO01746	blood
44	chr2:233727800-233738600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr2:233729200-233736400	Weak transcription	Fetal Muscle Trunk	muscle
46	chr2:233731000-233736800	Weak transcription	Rectal Mucosa Donor 31	rectum
47	chr2:233732600-233738200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr2:233734000-233737200	Enhancers	Brain Anterior Caudate	brain
49	chr2:233734200-233736800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr2:233734200-233739600	Flanking Active TSS	HepG2	liver

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