Variant report

Variant	rs6003540
Chromosome Location	chr22:23521698-23521699
allele	C/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	TBL1XR1	chr22:23520604-23527305	K562	blood:	n/a	n/a
2	TBL1XR1	chr22:23520619-23523842	K562	blood:	n/a	n/a
3	HDAC2	chr22:23520523-23526205	K562	blood:	n/a	chr22:23521032-23521051
4	POLR2A	chr22:23520633-23526356	K562	blood:	n/a	n/a
5	CUX1	chr22:23520618-23522723	K562	blood:	n/a	chr22:23521379-23521393
6	STAT5A	chr22:23520445-23522610	K562	blood:	n/a	chr22:23521510-23521521 chr22:23522547-23522559
7	EP300	chr22:23520596-23523878	K562	blood:	n/a	chr22:23522854-23522870 chr22:23521047-23521060 chr22:23522997-23523010 chr22:23521637-23521650
8	MYC	chr22:23521693-23523755	K562	blood:	n/a	chr22:23522597-23522607
9	MYC	chr22:23521697-23521709	HepG2	liver:	n/a	n/a
10	CTCF	chr22:23521620-23521770	GM12864	blood:	n/a	n/a
11	UBTF	chr22:23520613-23526470	K562	blood:	n/a	n/a
12	ELK1	chr22:23521501-23523446	K562	blood:	n/a	n/a
13	POLR2A	chr22:23521095-23526502	K562	blood:	n/a	n/a
14	TAL1	chr22:23520659-23522885	K562	blood:	n/a	n/a
15	RAD21	chr22:23520593-23521796	K562	blood:	n/a	chr22:23520806-23520816 chr22:23520806-23520818 chr22:23520801-23520820 chr22:23520804-23520817
16	TEAD4	chr22:23520448-23527326	K562	blood:	n/a	n/a
17	POLR2A	chr22:23521572-23527572	K562	blood:	n/a	n/a
18	STAT3	chr22:23521635-23521906	MCF10A-Er-Src	breast:	n/a	n/a
19	TBP	chr22:23520623-23526179	K562	blood:	n/a	n/a
20	MAX	chr22:23521486-23525908	K562	blood:	n/a	chr22:23524440-23524449 chr22:23525734-23525744 chr22:23524440-23524449 chr22:23522597-23522607 chr22:23524441-23524448
21	ZBTB7A	chr22:23521531-23525286	K562	blood:	n/a	chr22:23522591-23522599 chr22:23522590-23522598
22	MAX	chr22:23521593-23524918	HepG2	liver:	n/a	chr22:23524440-23524449 chr22:23524440-23524449 chr22:23522597-23522607 chr22:23524441-23524448
23	ZC3H11A	chr22:23520594-23526970	K562	blood:	n/a	n/a
24	MXI1	chr22:23521664-23521948	GM12878	blood:	n/a	n/a
25	FOSL1	chr22:23520529-23522897	K562	blood:	n/a	chr22:23522595-23522604
26	STAT3	chr22:23521628-23521957	MCF10A-Er-Src	breast:	n/a	n/a
27	EBF1	chr22:23521362-23522060	GM12878	blood:	n/a	chr22:23521612-23521621 chr22:23521610-23521621 chr22:23521611-23521621
28	ESR1	chr22:23521497-23521971	ECC-1	luminal epithelium:	n/a	chr22:23521732-23521747 chr22:23521731-23521748
29	MAX	chr22:23520537-23526174	K562	blood:	n/a	chr22:23524440-23524449 chr22:23525734-23525744 chr22:23524440-23524449 chr22:23522597-23522607 chr22:23524441-23524448
30	MAX	chr22:23521643-23523309	HepG2	liver:	n/a	chr22:23522597-23522607
31	GTF2F1	chr22:23520624-23526023	K562	blood:	n/a	n/a
32	MYC	chr22:23520609-23526146	K562	blood:	n/a	chr22:23524440-23524449 chr22:23525734-23525744 chr22:23524440-23524449 chr22:23522597-23522607 chr22:23524441-23524448
33	CBX3	chr22:23520451-23527677	K562	blood:	n/a	chr22:23520879-23520890
34	RAD21	chr22:23520451-23522047	SK-N-SH	brain:	n/a	chr22:23520806-23520816 chr22:23520806-23520818 chr22:23520801-23520820 chr22:23520804-23520817
35	RCOR1	chr22:23521635-23521827	HepG2	liver:	n/a	n/a
36	MXI1	chr22:23521576-23523276	HepG2	liver:	n/a	n/a
37	EBF1	chr22:23521498-23521699	GM12878	blood:	n/a	chr22:23521612-23521621 chr22:23521610-23521621 chr22:23521611-23521621
38	RFX5	chr22:23520628-23522640	K562	blood:	n/a	n/a
39	FOS	chr22:23521638-23521906	MCF10A-Er-Src	breast:	n/a	n/a
40	ESR1	chr22:23521508-23521927	ECC-1	luminal epithelium:	n/a	chr22:23521732-23521747 chr22:23521731-23521748
41	PML	chr22:23520528-23526389	K562	blood:	n/a	n/a
42	TEAD4	chr22:23520525-23527111	K562	blood:	n/a	n/a
43	POLR2A	chr22:23521544-23525860	K562	blood:	n/a	n/a
44	ZNF263	chr22:23520618-23525299	K562	blood:	n/a	chr22:23521369-23521378 chr22:23524591-23524600 chr22:23524513-23524522 chr22:23524594-23524603
45	HCFC1	chr22:23520599-23526421	K562	blood:	n/a	n/a
46	ARID3A	chr22:23521656-23523361	K562	blood:	n/a	n/a
47	BACH1	chr22:23520646-23522641	K562	blood:	n/a	n/a
48	HEY1	chr22:23521612-23524725	K562	blood:	n/a	chr22:23522874-23522889
49	NR2F2	chr22:23520429-23522955	K562	blood:	n/a	n/a
50	MAFK	chr22:23520595-23522722	K562	blood:	n/a	chr22:23521729-23521739

No.	Distal block	Cell Line	Cell type
1	chr12:120728308..120731053-chr22:23519442..23522442,4	MCF-7	breast:
2	chr22:23520289..23523680-chr22:23623216..23625593,134	K562	blood:
3	chr22:23520909..23526395-chr22:23622717..23628021,9	MCF-7	breast:
4	chr22:23520356..23521778-chr9:133741049..133742733,6	K562	blood:
5	chr12:120728297..120729929-chr22:23519462..23522442,4	MCF-7	breast:
6	chr22:23519615..23526434-chr22:23614924..23625964,20	MCF-7	breast:
7	chr22:23521185..23525273-chr22:23592606..23595379,3	MCF-7	breast:
8	chr22:23521575..23523250-chr22:23605169..23607302,2	MCF-7	breast:
9	chr22:23155103..23157714-chr22:23521587..23523946,2	K562	blood:
10	chr12:120728333..120732236-chr22:23519442..23524202,7	K562	blood:

Variant related genes	Relation type
BCR	TF binding region
ENSG00000226477	Chromatin interaction
ENSG00000202538	Chromatin interaction
ENSG00000200795	Chromatin interaction
ENSG00000186716	Chromatin interaction
ENSG00000230701	Chromatin interaction

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs12157412	1.00[AMR][1000 genomes]
rs12157536	1.00[AMR][1000 genomes]
rs12157941	1.00[AMR][1000 genomes]
rs12158986	1.00[AMR][1000 genomes]
rs12159793	1.00[AMR][1000 genomes]
rs12160027	1.00[AMR][1000 genomes]
rs12160099	1.00[AMR][1000 genomes]
rs2330366	1.00[AMR][1000 genomes]
rs5996469	1.00[AMR][1000 genomes]
rs5996472	1.00[AMR][1000 genomes]
rs5996477	1.00[AMR][1000 genomes]
rs5996478	0.88[AFR][1000 genomes]
rs5996479	1.00[AMR][1000 genomes]
rs5996480	1.00[AMR][1000 genomes]
rs5996481	1.00[AMR][1000 genomes]
rs5996482	1.00[AMR][1000 genomes]
rs5996484	1.00[AMR][1000 genomes]
rs6003521	1.00[AMR][1000 genomes]
rs6003522	1.00[AMR][1000 genomes]
rs6003523	1.00[AMR][1000 genomes]
rs6003524	1.00[AMR][1000 genomes]
rs6003526	1.00[AMR][1000 genomes]
rs6003528	1.00[AMR][1000 genomes]
rs6003530	1.00[AMR][1000 genomes]
rs6003537	1.00[AMR][1000 genomes]
rs6003538	1.00[AMR][1000 genomes]
rs6003539	1.00[AMR][1000 genomes]
rs6003541	1.00[AMR][1000 genomes]
rs6003542	1.00[AMR][1000 genomes]
rs6003543	1.00[AMR][1000 genomes]
rs6003545	1.00[AMR][1000 genomes]
rs6003546	1.00[AMR][1000 genomes]
rs6003548	1.00[AMR][1000 genomes]
rs6003549	1.00[AMR][1000 genomes]
rs6003628	1.00[AMR][1000 genomes]
rs9620237	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:26 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv915235	chr22:22971768-23650987	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	101 gene(s)	inside rSNPs	diseases
2	esv3388845	chr22:22973346-23652447	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	100 gene(s)	inside rSNPs	diseases
3	nsv531799	chr22:22993679-23642142	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
4	nsv1061433	chr22:22997799-23649107	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
5	nsv521695	chr22:22998337-23648009	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
6	nsv915236	chr22:22998337-23650987	Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
7	nsv588512	chr22:22998337-23667731	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	99 gene(s)	inside rSNPs	diseases
8	nsv531800	chr22:23002708-23648163	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
9	nsv916593	chr22:23002709-23648790	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers 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 miRNA	97 gene(s)	inside rSNPs	diseases
10	nsv993496	chr22:23002709-23654222	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
11	nsv1067002	chr22:23007167-23643363	Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers 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 miRNA	97 gene(s)	inside rSNPs	diseases
12	nsv1067324	chr22:23007367-23654223	Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
13	nsv533839	chr22:23012013-23643223	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
14	nsv916933	chr22:23012069-23654237	Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
15	nsv531801	chr22:23028586-23657804	Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	92 gene(s)	inside rSNPs	diseases
16	nsv531802	chr22:23046186-23627391	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	85 gene(s)	inside rSNPs	diseases
17	nsv1060509	chr22:23055148-23648719	Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	83 gene(s)	inside rSNPs	diseases
18	nsv1056324	chr22:23055148-23750989	Active TSS Weak transcription Genic enhancers Enhancers Strong transcription Flanking 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 miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
19	nsv1062780	chr22:23060449-23648719	Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	82 gene(s)	inside rSNPs	diseases
20	nsv948942	chr22:23063178-23645718	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	82 gene(s)	inside rSNPs	diseases
21	nsv1063200	chr22:23097177-23643224	Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	80 gene(s)	inside rSNPs	diseases
22	nsv949250	chr22:23157485-23645718	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	69 gene(s)	inside rSNPs	diseases
23	nsv1057659	chr22:23400739-24138788	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
24	nsv1058604	chr22:23497533-23545751	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
25	esv3365113	chr22:23521252-23524950	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
26	esv3373787	chr22:23521577-23524125	Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:23490400-23522000	Weak transcription	Aorta	Aorta
2	chr22:23516000-23522000	Enhancers	Primary T cells fromperipheralblood	blood
3	chr22:23517800-23522000	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr22:23517800-23522200	Enhancers	GM12878-XiMat	blood
5	chr22:23518000-23522000	Enhancers	Esophagus	oesophagus
6	chr22:23518000-23522200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr22:23519200-23522200	Enhancers	Primary B cells from peripheral blood	blood
8	chr22:23519400-23522000	Weak transcription	Thymus	Thymus
9	chr22:23519400-23522200	Enhancers	Primary neutrophils fromperipheralblood	blood
10	chr22:23519600-23521800	Enhancers	Primary T killer memory cells from peripheral blood	blood
11	chr22:23519600-23522000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr22:23519600-23522000	Enhancers	Placenta	Placenta
13	chr22:23519600-23522200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
14	chr22:23519800-23522000	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr22:23519800-23522000	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr22:23519800-23522200	Enhancers	Primary B cells from cord blood	blood
17	chr22:23520200-23521800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr22:23520600-23521800	Enhancers	Brain Anterior Caudate	brain
19	chr22:23520600-23521800	Enhancers	Brain Hippocampus Middle	brain
20	chr22:23520600-23522000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr22:23520600-23522000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr22:23520600-23522000	Enhancers	Primary T helper cells fromperipheralblood	blood
23	chr22:23520600-23522000	Enhancers	Brain Cingulate Gyrus	brain
24	chr22:23520600-23522000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
25	chr22:23520600-23522000	Enhancers	Pancreas	Pancrea
26	chr22:23520600-23522200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr22:23520600-23522200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
28	chr22:23520600-23522200	Bivalent Enhancer	Fetal Muscle Leg	muscle
29	chr22:23520600-23522200	Enhancers	Fetal Thymus	thymus
30	chr22:23520600-23522400	Flanking Active TSS	Stomach Smooth Muscle	stomach
31	chr22:23520800-23521800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr22:23520800-23521800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr22:23520800-23521800	Enhancers	Primary T helper naive cells from peripheral blood	blood
34	chr22:23520800-23521800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr22:23520800-23521800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr22:23520800-23521800	Enhancers	Adipose Nuclei	Adipose
37	chr22:23520800-23521800	Enhancers	Liver	Liver
38	chr22:23520800-23521800	Enhancers	Rectal Mucosa Donor 31	rectum
39	chr22:23520800-23521800	Enhancers	Rectal Smooth Muscle	rectum
40	chr22:23520800-23521800	Enhancers	Dnd41	blood
41	chr22:23520800-23521800	Flanking Active TSS	HepG2	liver
42	chr22:23520800-23522000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr22:23520800-23522000	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr22:23520800-23522000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr22:23520800-23522000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
46	chr22:23520800-23522000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
47	chr22:23520800-23522000	Enhancers	Muscle Satellite Cultured Cells	--
48	chr22:23520800-23522000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr22:23520800-23522000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr22:23520800-23522000	Enhancers	Brain Substantia Nigra	brain

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