Variant report

Variant	rs5751590
Chromosome Location	chr22:23486830-23486831
allele	A/C
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	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	HCFC1	chr22:23486827-23487930	K562	blood:	n/a	n/a
7	RCOR1	chr22:23486448-23488248	K562	blood:	n/a	n/a
8	ZNF384	chr22:23486148-23487835	K562	blood:	n/a	n/a
9	ZC3H11A	chr22:23486406-23488413	K562	blood:	n/a	n/a
10	BACH1	chr22:23486347-23488081	K562	blood:	n/a	n/a
11	STAT5A	chr22:23486255-23487443	K562	blood:	n/a	n/a
12	MAX	chr22:23486684-23489018	K562	blood:	n/a	chr22:23487429-23487439 chr22:23487465-23487474
13	TBL1XR1	chr22:23486350-23488289	K562	blood:	n/a	n/a
14	ELF1	chr22:23486235-23488516	K562	blood:	n/a	chr22:23487430-23487442
15	EGR1	chr22:23486809-23487945	K562	blood:	n/a	chr22:23487437-23487451 chr22:23487438-23487445 chr22:23487429-23487439 chr22:23487828-23487838 chr22:23487431-23487444 chr22:23487430-23487440 chr22:23487438-23487451 chr22:23487409-23487422 chr22:23487437-23487452 chr22:23487328-23487335 chr22:23487830-23487843
16	CBX3	chr22:23486307-23488415	K562	blood:	n/a	n/a
17	RCOR1	chr22:23486733-23487912	K562	blood:	n/a	n/a
18	NR2F2	chr22:23486304-23488700	K562	blood:	n/a	n/a
19	BHLHE40	chr22:23486757-23488118	K562	blood:	n/a	n/a

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:

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

Extended variants
information (count: 89 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs1051875	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13054985	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13407	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1987042	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1987043	0.82[ASN][1000 genomes]
rs2106109	0.82[ASN][1000 genomes]
rs2157709	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2157710	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2249692	0.86[ASN][1000 genomes]
rs2267000	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2267001	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2267002	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2267003	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2267004	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2267005	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2283803	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2301554	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3788347	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3788348	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3788349	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3788350	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3788351	0.85[EUR][1000 genomes]
rs3827316	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4820537	0.81[ASN][1000 genomes]
rs4820539	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4820541	0.80[ASN][1000 genomes]
rs4822356	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4822357	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4822358	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4822359	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4822360	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4822361	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4822362	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs5751587	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs5751589	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs5759590	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs5759593	0.89[ASN][1000 genomes]
rs5759594	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs5759595	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs5759596	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs5759598	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs5759600	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs5759604	0.82[ASN][1000 genomes]
rs5759607	0.81[ASN][1000 genomes]
rs5759611	0.80[ASN][1000 genomes]
rs5759616	0.80[ASN][1000 genomes]
rs5996470	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6003518	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs737846	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs756631	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs885963	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs885964	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs885965	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs916583	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs916584	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs916585	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9612237	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9612244	0.86[ASN][1000 genomes]
rs9612251	0.83[ASN][1000 genomes]
rs9624033	0.82[EUR][1000 genomes];0.91[ASN][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

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs5751590	BCR	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:113 , 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	chr22:23482200-23487000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
4	chr22:23483600-23487000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
5	chr22:23484200-23487200	Weak transcription	Right Ventricle	heart
6	chr22:23484200-23487600	Weak transcription	Left Ventricle	heart
7	chr22:23484400-23487000	Weak transcription	HSMMtube	muscle
8	chr22:23484400-23487600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr22:23484600-23487000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr22:23484600-23487000	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr22:23484600-23487000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr22:23484600-23487000	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr22:23484600-23487000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr22:23484600-23487000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr22:23484600-23487000	Weak transcription	Fetal Heart	heart
16	chr22:23484600-23487000	Weak transcription	Ovary	ovary
17	chr22:23484600-23487000	Weak transcription	NH-A	brain
18	chr22:23484600-23487000	Weak transcription	NHDF-Ad	bronchial
19	chr22:23484600-23487000	Weak transcription	NHLF	lung
20	chr22:23484600-23487200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr22:23484600-23487200	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr22:23484600-23487200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr22:23484600-23487200	Weak transcription	Fetal Lung	lung
24	chr22:23484600-23487200	Weak transcription	HSMM	muscle
25	chr22:23484600-23487600	Weak transcription	Placenta Amnion	Placenta Amnion
26	chr22:23484600-23487600	Weak transcription	Psoas Muscle	Psoas
27	chr22:23484800-23487000	Enhancers	Primary B cells from peripheral blood	blood
28	chr22:23484800-23487000	Enhancers	Primary T cells from cord blood	blood
29	chr22:23484800-23487000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
30	chr22:23484800-23487000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr22:23484800-23487000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr22:23484800-23487000	Weak transcription	Brain Germinal Matrix	brain
33	chr22:23484800-23487000	Weak transcription	Fetal Brain Female	brain
34	chr22:23484800-23487000	Enhancers	Fetal Intestine Small	intestine
35	chr22:23484800-23487000	Weak transcription	HUVEC	blood vessel
36	chr22:23484800-23487200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr22:23484800-23487400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr22:23485000-23487000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr22:23485000-23487000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr22:23485000-23487000	Enhancers	Primary T helper naive cells from peripheral blood	blood
41	chr22:23485000-23487000	Enhancers	Primary T killer memory cells from peripheral blood	blood
42	chr22:23485000-23487000	Weak transcription	Brain Inferior Temporal Lobe	brain
43	chr22:23485000-23487000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
44	chr22:23485000-23487000	Weak transcription	Brain Substantia Nigra	brain
45	chr22:23485000-23487000	Weak transcription	Duodenum Smooth Muscle	Duodenum
46	chr22:23485000-23487000	Weak transcription	Fetal Stomach	stomach
47	chr22:23485000-23487200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr22:23485000-23487600	Weak transcription	Fetal Brain Male	brain
49	chr22:23485000-23487600	Weak transcription	Lung	lung
50	chr22:23485200-23487000	Enhancers	Primary T helper naive cells fromperipheralblood	blood

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