Variant report

Variant	rs717923
Chromosome Location	chr1:92295724-92295725
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	REST	chr1:92295663-92296215	PFSK-1	brain:	n/a	chr1:92295965-92295974 chr1:92295960-92295980 chr1:92295960-92295980
2	REST	chr1:92295663-92296201	PFSK-1	brain:	n/a	chr1:92295965-92295974 chr1:92295960-92295980 chr1:92295960-92295980
3	MYC	chr1:92295704-92296133	MCF10A-Er-Src	breast:	n/a	n/a
4	NFIC	chr1:92295629-92296202	ECC-1	luminal epithelium:	n/a	n/a
5	SP1	chr1:92295665-92296239	A549	lung:	n/a	n/a
6	REST	chr1:92295720-92296122	PANC-1	pancreas:	n/a	chr1:92295965-92295974 chr1:92295960-92295980 chr1:92295960-92295980
7	MAZ	chr1:92295653-92295767	GM12878	blood:	n/a	n/a
8	POLR2A	chr1:92295625-92296315	MCF10A-Er-Src	breast:	n/a	n/a
9	TFAP2A	chr1:92295716-92296222	Hela-S3	cervix:	n/a	chr1:92295980-92295990 chr1:92295980-92295990 chr1:92295864-92295875 chr1:92295980-92295990 chr1:92295980-92295990
10	NFIC	chr1:92295717-92296172	SK-N-SH	brain:	n/a	n/a
11	POLR2A	chr1:92295590-92297246	HepG2	liver:	n/a	n/a
12	NFIC	chr1:92295664-92296218	ECC-1	luminal epithelium:	n/a	n/a
13	POLR2A	chr1:92295660-92296237	MCF10A-Er-Src	breast:	n/a	n/a
14	RCOR1	chr1:92295319-92297229	IMR90	lung:	n/a	n/a
15	CTCF	chr1:92295491-92296316	A549	lung:	n/a	n/a
16	TFAP2C	chr1:92295647-92296345	Hela-S3	cervix:	n/a	n/a
17	CTCF	chr1:92295704-92296167	A549	lung:	n/a	n/a

Variant related genes	Relation type
RN7SL653P	TF binding region

Extended variants
information (count: 100 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:78)

rs_ID	r²[population]
rs1032255	0.86[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10874980	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[YRI][hapmap];0.89[ASN][1000 genomes]
rs11165578	0.91[CHB][hapmap];0.91[JPT][hapmap];0.86[ASN][1000 genomes]
rs11576557	0.86[JPT][hapmap]
rs11799400	0.87[JPT][hapmap];0.84[EUR][1000 genomes]
rs12027931	0.82[JPT][hapmap];0.84[EUR][1000 genomes]
rs1352438	0.95[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1805109	0.86[JPT][hapmap];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1805110	0.86[JPT][hapmap];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1906586	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2046737	0.86[JPT][hapmap];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2087300	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2129972	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2129973	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2256471	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2265863	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2391070	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2450926	0.86[JPT][hapmap];0.83[EUR][1000 genomes]
rs2450927	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2489169	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2489170	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2489171	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2489176	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2489178	1.00[CHB][hapmap];0.95[JPT][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2489184	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2489185	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2489186	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2489192	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2634019	0.86[JPT][hapmap];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2634020	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2634022	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2634023	0.86[JPT][hapmap];0.85[EUR][1000 genomes]
rs2634024	0.86[JPT][hapmap];0.85[EUR][1000 genomes]
rs2634025	0.86[JPT][hapmap];0.85[EUR][1000 genomes]
rs2634026	0.85[EUR][1000 genomes]
rs2634027	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2634028	0.86[JPT][hapmap];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2634029	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2634030	0.86[JPT][hapmap];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2634032	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2634033	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2634034	0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2634036	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2799512	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2799514	0.85[EUR][1000 genomes]
rs2799515	0.85[EUR][1000 genomes]
rs2799516	0.95[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2799517	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2799521	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2799522	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2799523	0.89[JPT][hapmap];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2799524	0.86[JPT][hapmap];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2799525	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2799526	0.85[JPT][hapmap]
rs2799539	0.95[CHB][hapmap];1.00[JPT][hapmap];0.80[YRI][hapmap];0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2799547	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2810903	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs284141	0.84[EUR][1000 genomes]
rs284146	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs284148	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs284150	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs284151	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs284156	0.91[CHB][hapmap];0.87[JPT][hapmap];0.87[ASN][1000 genomes]
rs284157	0.91[CHB][hapmap];0.91[JPT][hapmap];0.87[ASN][1000 genomes]
rs284160	0.83[JPT][hapmap];0.89[YRI][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs284161	0.83[JPT][hapmap];0.87[YRI][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs284162	0.87[JPT][hapmap];1.00[YRI][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs284163	0.87[JPT][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs284164	0.87[JPT][hapmap];1.00[YRI][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3103332	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3103333	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs428815	0.87[JPT][hapmap];0.88[YRI][hapmap]
rs449960	0.85[CHB][hapmap];0.90[JPT][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7550856	0.86[JPT][hapmap];0.84[EUR][1000 genomes]
rs901913	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs901914	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs901915	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs901917	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012864	chr1:92067100-92827761	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	nsv535029	chr1:92067100-92827761	Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
3	nsv530438	chr1:92091957-92827760	Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
4	nsv1010179	chr1:92140209-92655952	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv535030	chr1:92140209-92655952	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
6	nsv1005917	chr1:92189945-92378683	Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv949449	chr1:92211020-92585831	Strong transcription Enhancers Genic enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
8	nsv524845	chr1:92215725-92598705	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
9	nsv462517	chr1:92215725-92598705	Weak transcription Bivalent Enhancer Enhancers Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
10	nsv546810	chr1:92215725-92598705	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
11	nsv1006318	chr1:92216408-92608324	Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
12	nsv432498	chr1:92218245-92618323	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
13	nsv1004570	chr1:92220544-92622129	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
14	nsv1007661	chr1:92220544-92655952	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
15	nsv1014837	chr1:92233905-92618839	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
16	nsv535031	chr1:92233905-92618839	Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
17	nsv1012134	chr1:92235485-92598800	Weak transcription Genic enhancers Flanking Active TSS Active TSS Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
18	nsv546818	chr1:92236048-92579206	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
19	nsv546819	chr1:92256626-92558583	Strong transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
20	nsv546820	chr1:92273644-92558583	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
21	nsv530046	chr1:92277460-92799794	Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
22	nsv1007270	chr1:92289298-92598800	Active TSS Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:80 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:92287600-92296000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr1:92291600-92296600	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr1:92292400-92297000	Enhancers	Placenta	Placenta
4	chr1:92293000-92295800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr1:92293000-92295800	Enhancers	Skeletal Muscle Male	skeletal muscle
6	chr1:92293000-92296000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr1:92293000-92296200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr1:92293200-92296200	Enhancers	Small Intestine	intestine
9	chr1:92293200-92296800	Enhancers	Right Atrium	heart
10	chr1:92293200-92297000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
11	chr1:92293400-92296400	Enhancers	Duodenum Mucosa	Duodenum
12	chr1:92293400-92296800	Enhancers	Esophagus	oesophagus
13	chr1:92293400-92296800	Enhancers	Left Ventricle	heart
14	chr1:92293400-92297200	Enhancers	Fetal Muscle Leg	muscle
15	chr1:92293400-92297600	Enhancers	Fetal Kidney	kidney
16	chr1:92293400-92298000	Enhancers	Fetal Heart	heart
17	chr1:92293600-92295800	Weak transcription	Brain Cingulate Gyrus	brain
18	chr1:92293600-92296200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
19	chr1:92293600-92296200	Weak transcription	Aorta	Aorta
20	chr1:92293600-92297000	Enhancers	Psoas Muscle	Psoas
21	chr1:92293800-92295800	Weak transcription	Brain Angular Gyrus	brain
22	chr1:92293800-92295800	Weak transcription	Brain Substantia Nigra	brain
23	chr1:92294000-92296000	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr1:92294000-92296200	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr1:92294000-92296800	Enhancers	Fetal Muscle Trunk	muscle
26	chr1:92294000-92296800	Enhancers	Spleen	Spleen
27	chr1:92294000-92297000	Enhancers	Right Ventricle	heart
28	chr1:92294200-92295800	Weak transcription	Brain Anterior Caudate	brain
29	chr1:92294200-92296800	Enhancers	Lung	lung
30	chr1:92294200-92297200	Enhancers	Ovary	ovary
31	chr1:92294200-92297800	Enhancers	Liver	Liver
32	chr1:92294400-92295800	Genic enhancers	Primary T cells fromperipheralblood	blood
33	chr1:92294400-92295800	Weak transcription	Primary T helper cells fromperipheralblood	blood
34	chr1:92294400-92295800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
35	chr1:92294400-92296200	Enhancers	Rectal Mucosa Donor 29	rectum
36	chr1:92294400-92296400	Enhancers	Skeletal Muscle Female	skeletal muscle
37	chr1:92294600-92295800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
38	chr1:92294600-92296200	Weak transcription	K562	blood
39	chr1:92294600-92298200	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr1:92294600-92298600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr1:92294800-92295800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr1:92294800-92296000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr1:92294800-92297000	Enhancers	Pancreas	Pancrea
44	chr1:92294800-92311600	Weak transcription	Gastric	stomach
45	chr1:92295000-92295800	Enhancers	Colonic Mucosa	Colon
46	chr1:92295000-92296200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr1:92295000-92296200	Enhancers	Rectal Smooth Muscle	rectum
48	chr1:92295000-92296400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr1:92295200-92295800	Enhancers	A549	lung
50	chr1:92295200-92296200	Enhancers	Adipose Nuclei	Adipose

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