Variant report

Variant	rs2636739
Chromosome Location	chr4:106352105-106352106
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:106351251..106353163-chr4:106388655..106390635,2	K562	blood:

Extended variants
information (count: 151 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:144)

rs_ID	r²[population]
rs10015293	0.83[ASN][1000 genomes]
rs11733020	0.91[ASN][1000 genomes]
rs12643660	0.89[CEU][hapmap];0.80[CHB][hapmap];1.00[GIH][hapmap];0.83[TSI][hapmap];0.80[ASN][1000 genomes]
rs13134204	0.94[ASN][1000 genomes]
rs1344330	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13787	0.95[CHB][hapmap];0.89[CHD][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs1490590	0.94[ASN][1000 genomes]
rs1490591	0.95[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1490592	0.94[ASN][1000 genomes]
rs1490593	0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs1490594	0.93[ASN][1000 genomes]
rs1490595	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs1490603	0.94[ASN][1000 genomes]
rs1490604	0.95[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs1490605	0.94[ASN][1000 genomes]
rs1490606	0.94[ASN][1000 genomes]
rs1490607	0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs1490608	0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs1565484	0.94[ASN][1000 genomes]
rs1565485	0.80[ASN][1000 genomes]
rs1844656	0.94[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs1994636	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.82[YRI][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1994637	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2077608	1.00[CHB][hapmap];1.00[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap];0.82[YRI][hapmap];0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2130693	0.93[AFR][1000 genomes];0.85[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs2130694	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[YRI][hapmap];0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs2172028	0.94[ASN][1000 genomes]
rs2466916	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2522545	0.95[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs2636696	0.95[CHB][hapmap];0.95[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.91[ASN][1000 genomes]
rs2636698	0.95[CHB][hapmap];0.95[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.92[ASN][1000 genomes]
rs2636700	0.84[ASN][1000 genomes]
rs2636701	0.94[ASN][1000 genomes]
rs2636703	0.94[ASN][1000 genomes]
rs2636704	0.94[ASN][1000 genomes]
rs2636706	0.94[ASN][1000 genomes]
rs2636707	0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs2636708	0.95[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs2636709	0.94[ASN][1000 genomes]
rs2636711	0.98[ASN][1000 genomes]
rs2636712	0.90[ASN][1000 genomes]
rs2636713	0.82[ASW][hapmap];0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.81[MKK][hapmap];0.80[TSI][hapmap]
rs2636716	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2636718	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2636720	0.94[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs2636721	0.90[ASN][1000 genomes]
rs2636722	0.95[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs2636723	0.95[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs2636725	0.95[ASN][1000 genomes]
rs2636726	0.95[CHB][hapmap];0.89[CHD][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs2636728	0.94[ASN][1000 genomes]
rs2636729	0.95[CHB][hapmap];0.82[CHD][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs2636730	0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2636731	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.94[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2636732	1.00[CHB][hapmap];0.97[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.93[TSI][hapmap];0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2636733	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.94[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs2636734	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2636735	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2636737	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2636738	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2636741	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2636742	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2636743	1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap];0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2636746	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2636748	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2636749	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2636751	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2713822	0.86[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2713823	0.87[ASN][1000 genomes]
rs2713825	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2713827	0.94[CHB][hapmap];0.95[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.83[TSI][hapmap];0.95[ASN][1000 genomes]
rs2713828	0.84[ASN][1000 genomes]
rs2713829	0.95[CHB][hapmap];0.95[CHD][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap]
rs2713830	0.95[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs2713831	0.80[JPT][hapmap]
rs2713832	0.95[CHB][hapmap];0.89[CHD][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs2713833	0.95[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs2713834	0.95[CHB][hapmap];0.95[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.90[TSI][hapmap];0.83[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2713835	0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2713836	0.94[ASN][1000 genomes]
rs2713837	0.82[ASN][1000 genomes]
rs2713838	0.89[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.98[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2713839	0.91[ASN][1000 genomes]
rs2713840	0.98[ASN][1000 genomes]
rs2713841	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs2713842	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2713843	0.94[ASN][1000 genomes]
rs2713847	0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs2713850	0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs2713851	0.87[ASN][1000 genomes]
rs2713852	0.95[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs2713853	0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs2713854	0.95[CHB][hapmap];0.89[CHD][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs2713859	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs2713860	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2713861	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2713863	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2713864	0.97[ASN][1000 genomes]
rs2713866	0.94[ASN][1000 genomes]
rs2713867	0.94[ASN][1000 genomes]
rs2713868	0.94[ASN][1000 genomes]
rs2713869	0.94[ASN][1000 genomes]
rs2713870	0.94[ASN][1000 genomes]
rs2713871	0.84[JPT][hapmap];0.81[ASN][1000 genomes]
rs2713873	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.84[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2713874	1.00[CHB][hapmap];0.95[JPT][hapmap];0.93[YRI][hapmap];0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2713875	0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2713876	0.86[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2726453	0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs2726454	0.95[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2726455	0.95[CHB][hapmap];0.92[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.90[TSI][hapmap];0.84[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2726462	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2726463	0.94[AFR][1000 genomes];0.89[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2726468	0.86[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2726471	0.90[CHB][hapmap];0.81[CHD][hapmap];0.90[JPT][hapmap];0.97[ASN][1000 genomes]
rs2726472	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2726493	0.92[ASN][1000 genomes]
rs2726494	0.94[ASN][1000 genomes]
rs2726495	0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs2726497	0.85[ASN][1000 genomes]
rs2726499	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2726502	0.95[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs2726503	0.90[CHB][hapmap];0.89[CHD][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs2726506	0.95[CHB][hapmap];0.89[CHD][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs2726509	0.96[ASN][1000 genomes]
rs2726510	0.97[ASN][1000 genomes]
rs2726511	0.83[ASN][1000 genomes]
rs2726514	0.96[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2726515	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2726516	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2726526	0.84[CHB][hapmap];0.92[CHD][hapmap];0.90[JPT][hapmap];0.86[TSI][hapmap];0.88[ASN][1000 genomes]
rs2866884	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs4450931	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4467572	0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs6855177	0.92[ASN][1000 genomes]
rs716205	0.94[ASN][1000 genomes]
rs753972	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7673368	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs7693292	0.95[ASN][1000 genomes]
rs923587	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs923588	0.98[ASN][1000 genomes]
rs923589	0.94[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs923590	0.84[ASN][1000 genomes]
rs9992793	0.80[CHB][hapmap];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv461609	chr4:105869548-106366209	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
2	nsv470063	chr4:105869548-106366209	Transcr. at gene 5' and 3' Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
3	nsv595007	chr4:105869548-106366209	Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
4	nsv879699	chr4:106212562-106698892	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
5	nsv830027	chr4:106222010-106406738	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
6	nsv1002228	chr4:106346206-106433381	ZNF genes & repeats Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
7	esv2760858	chr4:106351454-106376197	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs2636739	OSTC	cis	parietal	SCAN
rs2636739	AGXT2L1	cis	parietal	SCAN
rs2636739	TET2	cis	parietal	SCAN

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:106287600-106357000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr4:106321400-106367200	Weak transcription	HUVEC	blood vessel
3	chr4:106321600-106356200	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr4:106321800-106353600	Weak transcription	HMEC	breast
5	chr4:106323600-106372800	Weak transcription	Stomach Mucosa	stomach
6	chr4:106326000-106356400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr4:106326000-106356600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr4:106326000-106363200	Weak transcription	Colon Smooth Muscle	Colon
9	chr4:106327200-106365200	Weak transcription	Osteobl	bone
10	chr4:106327200-106389200	Weak transcription	Small Intestine	intestine
11	chr4:106327200-106390600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr4:106330600-106356400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr4:106336600-106356400	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr4:106336800-106376400	Weak transcription	Right Ventricle	heart
15	chr4:106336800-106387800	Weak transcription	NHLF	lung
16	chr4:106337000-106354400	Weak transcription	Left Ventricle	heart
17	chr4:106337000-106354600	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr4:106337200-106356600	Weak transcription	Brain Cingulate Gyrus	brain
19	chr4:106340200-106387800	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr4:106341600-106376000	Weak transcription	Fetal Heart	heart
21	chr4:106343200-106363000	Weak transcription	Psoas Muscle	Psoas
22	chr4:106344000-106363800	Weak transcription	HepG2	liver
23	chr4:106344200-106352800	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr4:106345200-106354400	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr4:106345200-106354800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr4:106345200-106358800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr4:106346400-106354600	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr4:106346600-106354200	Weak transcription	NH-A	brain
29	chr4:106346600-106369000	Weak transcription	Hela-S3	cervix
30	chr4:106347200-106366000	Weak transcription	NHDF-Ad	bronchial
31	chr4:106347600-106355400	Weak transcription	K562	blood
32	chr4:106347600-106367600	Weak transcription	Fetal Brain Male	brain
33	chr4:106347600-106392800	Weak transcription	Colonic Mucosa	Colon
34	chr4:106347800-106352600	Weak transcription	A549	lung
35	chr4:106347800-106352800	Weak transcription	Primary B cells from peripheral blood	blood
36	chr4:106347800-106354600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr4:106347800-106354800	Weak transcription	HSMM	muscle
38	chr4:106347800-106357200	Weak transcription	Placenta Amnion	Placenta Amnion
39	chr4:106347800-106362800	Weak transcription	Spleen	Spleen
40	chr4:106347800-106375200	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr4:106348000-106354200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr4:106348000-106354400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr4:106348000-106354600	Weak transcription	NHEK	skin
44	chr4:106348000-106354800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
45	chr4:106348000-106356400	Weak transcription	Brain Hippocampus Middle	brain
46	chr4:106348000-106356600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
47	chr4:106348000-106366000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr4:106348000-106375000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr4:106348000-106376400	Weak transcription	Gastric	stomach
50	chr4:106348000-106376800	Weak transcription	Pancreas	Pancrea

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