Variant report

Variant	rs6003523
Chromosome Location	chr22:23486678-23486679
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:14)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:14 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr22:23486630-23488553	K562	blood:	n/a	n/a
2	ETS1	chr22:23486605-23487086	GM12878	blood:	n/a	n/a
3	HDAC2	chr22:23486603-23489476	K562	blood:	n/a	n/a
4	NRF1	chr22:23486456-23487718	K562	blood:	n/a	chr22:23487430-23487439 chr22:23487361-23487372
5	ZNF274	chr22:23486372-23488122	K562	blood:	n/a	n/a
6	RCOR1	chr22:23486448-23488248	K562	blood:	n/a	n/a
7	ZNF384	chr22:23486148-23487835	K562	blood:	n/a	n/a
8	ZC3H11A	chr22:23486406-23488413	K562	blood:	n/a	n/a
9	BACH1	chr22:23486347-23488081	K562	blood:	n/a	n/a
10	STAT5A	chr22:23486255-23487443	K562	blood:	n/a	n/a
11	TBL1XR1	chr22:23486350-23488289	K562	blood:	n/a	n/a
12	ELF1	chr22:23486235-23488516	K562	blood:	n/a	chr22:23487430-23487442
13	CBX3	chr22:23486307-23488415	K562	blood:	n/a	n/a
14	NR2F2	chr22:23486304-23488700	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:23486678-23486728	HRE	kidney:	n/a
2	chr22:23486678-23486728	HPAEpiC	pulmonary alveolar:	n/a
3	chr22:23486678-23486728	ProgFib	skin:	n/a
4	chr22:23486678-23486728	HepG2	liver:	n/a
5	chr22:23486678-23486728	HL-60	blood:	n/a
6	chr22:23486678-23486728	SK-N-SH	brain:	n/a
7	chr22:23486678-23486728	HAEpiC	amniotic membrane:	n/a
8	chr22:23486678-23486728	U87	brain:	n/a
9	chr22:23486678-23486728	AG10803	skin:	n/a
10	chr22:23486678-23486728	SK-N-SH_RA	brain:	n/a
11	chr22:23486678-23486728	RPTEC	kidney:	n/a
12	chr22:23486678-23486728	PrEC	prostate:	n/a
13	chr22:23486678-23486728	K562	blood:	n/a
14	chr22:23486678-23486728	LNCaP	prostate:	n/a
15	chr22:23486678-23486728	ECC-1	luminal epithelium:	n/a
16	chr22:23486678-23486728	NB4	blood:	n/a
17	chr22:23486678-23486728	Caco-2	colon:	n/a
18	chr22:23486678-23486728	HCM	heart:	n/a
19	chr22:23486678-23486728	IMR90	lung:	fetal
20	chr22:23486678-23486728	H1-hESC	embryonic stem cell:	embryo
21	chr22:23486678-23486728	HCPEpiC	choroid plexus:	n/a
22	chr22:23486678-23486728	HCT-116	colon:	n/a
23	chr22:23486678-23486728	GM19239	blood:	n/a
24	chr22:23486678-23486728	HMEC	breast:	n/a
25	chr22:23486678-23486728	GM12892	blood:	n/a
26	chr22:23486678-23486728	AG09319	gingival:	n/a
27	chr22:23486678-23486728	HEEpiC	esophagus:	n/a
28	chr22:23486678-23486728	HNPCEpiC	eye:	n/a
29	chr22:23486678-23486728	GM12891	blood:	n/a
30	chr22:23486678-23486728	HUVEC	blood vessel:	n/a
31	chr22:23486678-23486728	HCF	heart:	n/a
32	chr22:23486678-23486728	A549	lung:	n/a
33	chr22:23486678-23486728	PANC-1	pancreas:	n/a
34	chr22:23486678-23486728	AoSMC	blood vessel:	n/a
35	chr22:23486678-23486728	SKMC	muscle:	n/a
36	chr22:23486678-23486728	Hela-S3	cervix:	n/a
37	chr22:23486678-23486728	SAEC	small airway:	n/a
38	chr22:23486678-23486728	MCF-7	breast:	n/a
39	chr22:23486678-23486728	SK-N-MC	brain:	n/a
40	chr22:23486678-23486728	GM06990	blood:	n/a
41	chr22:23486678-23486728	Jurkat	blood:	n/a
42	chr22:23486678-23486728	BE2_C	brain:	n/a
43	chr22:23486678-23486728	HIPEpiC	eye:	n/a
44	chr22:23486678-23486728	CMK	blood:	n/a
45	chr22:23486678-23486728	NH-A	brain:	n/a
46	chr22:23486678-23486728	HRCEpiC	kidney:	n/a
47	chr22:23486678-23486728	GM12878	blood:	n/a
48	chr22:23486678-23486728	PFSK-1	brain:	n/a
49	chr22:23486678-23486728	AG09309	skin:	n/a
50	chr22:23486678-23486728	MCF10A-Er-Src	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr22:22900276..22902223-chr22:23486030..23487937,2	K562	blood:
2	chr22:23410484..23412785-chr22:23485960..23488893,2	K562	blood:
3	chr22:23484062..23485814-chr22:23485870..23488963,4	K562	blood:
4	chr22:23463055..23465071-chr22:23484358..23487240,2	K562	blood:

No data

Variant related genes	Relation type
RTDR1	TF binding region
RAB36	TF binding region
RAB36	CpG island
RTDR1	CpG island
ENSG00000185686	Chromatin interaction
ENSG00000100218	Chromatin interaction
ENSG00000128266	Chromatin interaction
ENSG00000220891	Chromatin interaction

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs12157412	1.00[AMR][1000 genomes]
rs12157536	0.84[AFR][1000 genomes];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	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12166415	1.00[AMR][1000 genomes]
rs2330366	1.00[AMR][1000 genomes]
rs5996469	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs5996472	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs5996477	1.00[AMR][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[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6003522	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6003524	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6003526	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6003528	1.00[AMR][1000 genomes]
rs6003530	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6003537	1.00[AMR][1000 genomes]
rs6003538	1.00[AMR][1000 genomes]
rs6003539	1.00[AMR][1000 genomes]
rs6003540	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]
rs9620191	1.00[AMR][1000 genomes]
rs9620237	1.00[AMR][1000 genomes]
rs9623975	1.00[AMR][1000 genomes]
rs9623976	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:29 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1803110	chr22:22731758-23497674	Flanking Active TSS Bivalent Enhancer Strong transcription Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
2	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	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
24	esv34158	chr22:23216762-23499513	Weak transcription Bivalent Enhancer Enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	53 gene(s)	inside rSNPs	diseases
25	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
26	nsv544616	chr22:23474827-23495231	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
27	esv1808801	chr22:23478573-23489042	Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
28	esv1812488	chr22:23478573-23489042	Flanking Active TSS Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
29	esv1801510	chr22:23478611-23491000	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:111 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:23479400-23487400	Weak transcription	Esophagus	oesophagus
2	chr22:23480000-23487000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr22:23482000-23486800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
4	chr22:23482200-23487000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
5	chr22:23483600-23487000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
6	chr22:23484200-23487200	Weak transcription	Right Ventricle	heart
7	chr22:23484200-23487600	Weak transcription	Left Ventricle	heart
8	chr22:23484400-23487000	Weak transcription	HSMMtube	muscle
9	chr22:23484400-23487600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr22:23484600-23486800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr22:23484600-23486800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr22:23484600-23486800	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr22:23484600-23486800	Weak transcription	HMEC	breast
14	chr22:23484600-23486800	Weak transcription	NHEK	skin
15	chr22:23484600-23486800	Weak transcription	Osteobl	bone
16	chr22:23484600-23487000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr22:23484600-23487000	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr22:23484600-23487000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr22:23484600-23487000	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr22:23484600-23487000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr22:23484600-23487000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr22:23484600-23487000	Weak transcription	Fetal Heart	heart
23	chr22:23484600-23487000	Weak transcription	Ovary	ovary
24	chr22:23484600-23487000	Weak transcription	NH-A	brain
25	chr22:23484600-23487000	Weak transcription	NHDF-Ad	bronchial
26	chr22:23484600-23487000	Weak transcription	NHLF	lung
27	chr22:23484600-23487200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr22:23484600-23487200	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr22:23484600-23487200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr22:23484600-23487200	Weak transcription	Fetal Lung	lung
31	chr22:23484600-23487200	Weak transcription	HSMM	muscle
32	chr22:23484600-23487600	Weak transcription	Placenta Amnion	Placenta Amnion
33	chr22:23484600-23487600	Weak transcription	Psoas Muscle	Psoas
34	chr22:23484800-23486800	Enhancers	Primary T cells fromperipheralblood	blood
35	chr22:23484800-23486800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
36	chr22:23484800-23486800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr22:23484800-23486800	Weak transcription	Brain Angular Gyrus	brain
38	chr22:23484800-23487000	Enhancers	Primary B cells from peripheral blood	blood
39	chr22:23484800-23487000	Enhancers	Primary T cells from cord blood	blood
40	chr22:23484800-23487000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
41	chr22:23484800-23487000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr22:23484800-23487000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr22:23484800-23487000	Weak transcription	Brain Germinal Matrix	brain
44	chr22:23484800-23487000	Weak transcription	Fetal Brain Female	brain
45	chr22:23484800-23487000	Enhancers	Fetal Intestine Small	intestine
46	chr22:23484800-23487000	Weak transcription	HUVEC	blood vessel
47	chr22:23484800-23487200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr22:23484800-23487400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr22:23485000-23486800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr22:23485000-23486800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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