Variant report

Variant	rs199525
Chromosome Location	chr17:44847834-44847835
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:44816270..44819088-chr17:44845691..44848257,2	MCF-7	breast:
2	chr17:44840766..44847017-chr17:44847800..44851001,9	MCF-7	breast:
3	chr17:44801247..44804412-chr17:44846741..44850099,3	K562	blood:
4	chr17:44837102..44839238-chr17:44845941..44848841,2	K562	blood:
5	chr17:44832715..44835385-chr17:44845501..44848268,3	K562	blood:
6	chr17:44830114..44832534-chr17:44845890..44849410,4	K562	blood:
7	chr17:44847827..44849684-chr17:44903325..44905972,2	K562	blood:
8	chr17:44808673..44811660-chr17:44847775..44850081,2	K562	blood:
9	chr17:44846909..44848699-chr17:44886329..44888882,2	K562	blood:
10	chr17:44846353..44850075-chr17:44870910..44874671,5	K562	blood:
11	chr17:44847668..44852830-chr17:44858394..44861796,5	MCF-7	breast:
12	chr17:44821369..44826185-chr17:44846753..44849990,6	K562	blood:
13	chr17:44846693..44849612-chr17:44868202..44870057,2	K562	blood:
14	chr17:44845310..44847853-chr17:44872083..44874051,2	K562	blood:
15	chr17:44846645..44849185-chr17:44896689..44899109,2	MCF-7	breast:
16	chr17:44804689..44809871-chr17:44845472..44850072,6	K562	blood:
17	chr17:44845867..44850393-chr17:44893846..44898781,9	K562	blood:
18	chr17:44847670..44850061-chr17:44912249..44914668,3	K562	blood:
19	chr17:44820992..44822869-chr17:44847358..44849527,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000073969	Chromatin interaction
ENSG00000108379	Chromatin interaction

Extended variants
information (count: 69 )
Associated
traits (count: 69 )

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs1378358	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs169201	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs199439	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs199443	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs199445	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs199447	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs199448	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs199451	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs199456	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs199457	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs199499	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs199502	0.84[EUR][1000 genomes]
rs199503	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs199504	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs199505	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs199506	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs199507	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs199509	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs199510	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs199512	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs199513	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs199514	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs199515	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs199516	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs199526	0.89[EUR][1000 genomes]
rs199528	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs199529	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs199533	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs199534	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs199535	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs415430	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs430685	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs538628	1.00[ASN][1000 genomes]
rs70600	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs70602	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs916888	1.00[ASN][1000 genomes]
rs9896243	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:32 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv431716	chr17:43893020-44868187	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer 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 target site	62 gene(s)	inside rSNPs	diseases
2	nsv431718	chr17:44094463-44873614	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
3	nsv431729	chr17:44144214-44869063	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
4	esv2757660	chr17:44162284-44868187	Enhancers Genic enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
5	nsv431805	chr17:44165803-44868430	Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS 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 miRNA target site	54 gene(s)	inside rSNPs	diseases
6	esv3492820	chr17:44174959-45161556	Weak transcription Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
7	esv3492821	chr17:44174959-45161556	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
8	nsv916432	chr17:44223908-44873614	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
9	esv3502492	chr17:44305975-45169159	Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
10	esv3502493	chr17:44305975-45169159	Active TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
11	esv1819056	chr17:44391822-44873614	Enhancers Strong transcription Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
12	esv1844763	chr17:44391822-44913631	Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
13	nsv428343	chr17:44391822-44913631	Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
14	esv1806073	chr17:44443111-44873614	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
15	nsv531823	chr17:44485771-45067769	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
16	esv1850605	chr17:44537030-44913631	Weak transcription Genic enhancers Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
17	esv1792649	chr17:44627136-44849634	Weak transcription Bivalent/Poised TSS Bivalent Enhancer Strong transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
18	esv1820936	chr17:44629166-44848916	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
19	esv1812673	chr17:44648058-44849188	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer 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 target site	15 gene(s)	inside rSNPs	diseases
20	esv1818423	chr17:44648058-44849634	Weak transcription Flanking Bivalent TSS/Enh Active TSS Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
21	esv1805955	chr17:44654416-44849188	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
22	esv1818944	chr17:44662268-44859144	Genic enhancers Weak transcription Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
23	esv1796587	chr17:44680207-44849634	Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
24	esv1803101	chr17:44680207-44849634	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
25	esv1803756	chr17:44680207-44865439	Strong transcription Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
26	nsv833465	chr17:44706496-44889749	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
27	esv1843460	chr17:44732200-44913631	Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
28	esv1810528	chr17:44814884-44849634	Genic enhancers Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region miRNA target site	13 gene(s)	inside rSNPs	diseases
29	esv1845488	chr17:44816132-44849634	Weak transcription Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region miRNA target site	13 gene(s)	inside rSNPs	diseases
30	nsv908562	chr17:44828931-45102413	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
31	nsv949295	chr17:44836653-45080757	Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	24 gene(s)	inside rSNPs	diseases
32	esv1846002	chr17:44841209-44849188	Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	13 gene(s)	inside rSNPs	diseases

mRNA abundance (count:69)

SNP	Gene	Cis/trans	Tissue	Source
rs199525	RP11-259G18.2	cis	Esophagus Mucosa	GTEx
rs199525	KANSL1-AS1	cis	lung	GTEx
rs199525	RP11-259G18.2	cis	lung	GTEx
rs199525	KANSL1-AS1	cis	Heart Left Ventricle	GTEx
rs199525	RP11-259G18.3	cis	Skin Sun Exposed Lower leg	GTEx
rs199525	LRRC37A	cis	Artery Aorta	GTEx
rs199525	RP11-259G18.3	cis	Thyroid	GTEx
rs199525	RP11-259G18.2	cis	Nerve Tibial	GTEx
rs199525	MAPT	cis	Esophagus Mucosa	GTEx
rs199525	KANSL1-AS1	cis	Esophagus Mucosa	GTEx
rs199525	KANSL1-AS1	cis	Whole Blood	GTEx
rs199525	KANSL1-AS1	cis	Esophagus Muscularis	GTEx
rs199525	RP11-259G18.2	cis	Whole Blood	GTEx
rs199525	RP11-259G18.2	cis	Muscle Skeletal	GTEx
rs199525	RP11-259G18.3	cis	Adipose Subcutaneous	GTEx
rs199525	LRRC37A2	cis	Artery Aorta	GTEx
rs199525	KANSL1-AS1	cis	Nerve Tibial	GTEx
rs199525	RP11-259G18.3	cis	Esophagus Mucosa	GTEx
rs199525	ARL17	Cis_1M	lymphoblastoid	RTeQTL
rs199525	LRRC37A	cis	Nerve Tibial	GTEx
rs199525	RP11-259G18.3	cis	Muscle Skeletal	GTEx
rs199525	LRRC37A	cis	Adipose Subcutaneous	GTEx
rs199525	RP11-259G18.3	cis	Artery Aorta	GTEx
rs199525	LRRC37A2	cis	Adipose Subcutaneous	GTEx
rs199525	LRRC37A	cis	Muscle Skeletal	GTEx
rs199525	RP11-259G18.3	cis	Stomach	GTEx
rs199525	RP11-259G18.3	cis	Whole Blood	GTEx
rs199525	RP11-259G18.2	cis	Adipose Subcutaneous	GTEx
rs199525	RP11-259G18.3	cis	Artery Tibial	GTEx
rs199525	KANSL1-AS1	cis	Artery Tibial	GTEx
rs199525	LRRC37A2	cis	Heart Left Ventricle	GTEx
rs199525	LRRC37A2	cis	Esophagus Muscularis	GTEx
rs199525	LRRC37A2	cis	Artery Tibial	GTEx
rs199525	LRRC37A2	cis	Stomach	GTEx
rs199525	LRRC37A2	cis	Nerve Tibial	GTEx
rs199525	RP11-259G18.3	cis	Esophagus Muscularis	GTEx
rs199525	RP11-259G18.2	cis	Stomach	GTEx
rs199525	RP11-259G18.2	cis	Esophagus Muscularis	GTEx
rs199525	RP11-259G18.2	cis	Skin Sun Exposed Lower leg	GTEx
rs199525	MAPK8IP1	trans	lymphoblastoid	RTeQTL
rs199525	RP11-259G18.3	cis	Nerve Tibial	GTEx
rs199525	LOC644246	Cis_1M	lymphoblastoid	RTeQTL
rs199525	LRRC37A	cis	lung	GTEx
rs199525	LRRC37A2	cis	Thyroid	GTEx
rs199525	LRRC37A2	cis	Whole Blood	GTEx
rs199525	KANSL1-AS1	cis	Artery Aorta	GTEx
rs199525	RP11-259G18.2	cis	Artery Tibial	GTEx
rs199525	LRRC37A4	Cis_chr	lymphoblastoid	RTeQTL
rs199525	LRRC37A2	cis	Muscle Skeletal	GTEx
rs199525	LRRC37A	cis	Esophagus Mucosa	GTEx
rs199525	LRRC37A	cis	Stomach	GTEx
rs199525	KANSL1-AS1	cis	Thyroid	GTEx
rs199525	RP11-259G18.2	cis	Thyroid	GTEx
rs199525	RP11-259G18.2	cis	Heart Left Ventricle	GTEx
rs199525	RP11-259G18.3	cis	lung	GTEx
rs199525	KANSL1-AS1	cis	Stomach	GTEx
rs199525	KANSL1-AS1	cis	Adipose Subcutaneous	GTEx
rs199525	LRRC37A	cis	Skin Sun Exposed Lower leg	GTEx
rs199525	LRRC37A	cis	Thyroid	GTEx
rs199525	KANSL1-AS1	cis	Skin Sun Exposed Lower leg	GTEx
rs199525	KANSL1-AS1	cis	Muscle Skeletal	GTEx
rs199525	LRRC37A2	cis	Skin Sun Exposed Lower leg	GTEx
rs199525	LRRC37A	cis	Artery Tibial	GTEx
rs199525	LRRC37A17P	cis	Esophagus Mucosa	GTEx
rs199525	LRRC37A	cis	Esophagus Muscularis	GTEx
rs199525	RP11-259G18.3	cis	Heart Left Ventricle	GTEx
rs199525	LRRC37A2	cis	lung	GTEx
rs199525	RP11-259G18.2	cis	Artery Aorta	GTEx
rs199525	WNT3	cis	Thyroid	GTEx

Chromatin state (count:105 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:44829800-44848000	Weak transcription	Fetal Kidney	kidney
2	chr17:44834600-44848000	Weak transcription	Brain Cingulate Gyrus	brain
3	chr17:44834600-44848400	Weak transcription	Aorta	Aorta
4	chr17:44843000-44848400	Weak transcription	Brain Angular Gyrus	brain
5	chr17:44843200-44848000	Weak transcription	NH-A	brain
6	chr17:44843200-44848200	Weak transcription	HMEC	breast
7	chr17:44843200-44848400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr17:44843400-44848000	Weak transcription	Left Ventricle	heart
9	chr17:44843400-44848200	Weak transcription	Pancreas	Pancrea
10	chr17:44843400-44848200	Weak transcription	HUVEC	blood vessel
11	chr17:44844000-44848200	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr17:44846800-44848000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr17:44846800-44848000	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
14	chr17:44846800-44848000	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
15	chr17:44846800-44848000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr17:44846800-44848000	Bivalent Enhancer	Brain Germinal Matrix	brain
17	chr17:44846800-44848000	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
18	chr17:44846800-44848000	Enhancers	Right Ventricle	heart
19	chr17:44846800-44848200	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
20	chr17:44846800-44848200	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
21	chr17:44846800-44848200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
22	chr17:44846800-44848200	Enhancers	NHDF-Ad	bronchial
23	chr17:44846800-44848400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr17:44846800-44848400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
25	chr17:44846800-44848400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
26	chr17:44846800-44848400	Enhancers	Fetal Brain Male	brain
27	chr17:44846800-44848400	Enhancers	Fetal Heart	heart
28	chr17:44846800-44848400	Enhancers	Lung	lung
29	chr17:44846800-44848400	Enhancers	Placenta Amnion	Placenta Amnion
30	chr17:44846800-44848600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
31	chr17:44846800-44848600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr17:44846800-44848600	Enhancers	Gastric	stomach
33	chr17:44847000-44848400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
34	chr17:44847000-44848800	Enhancers	Spleen	Spleen
35	chr17:44847000-44849600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr17:44847200-44848000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
37	chr17:44847200-44848000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
38	chr17:44847200-44848000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
39	chr17:44847200-44848000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr17:44847200-44848000	Weak transcription	NHLF	lung
41	chr17:44847200-44848200	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
42	chr17:44847200-44848200	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr17:44847200-44848800	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
44	chr17:44847400-44848000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
45	chr17:44847400-44848000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr17:44847400-44848000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr17:44847400-44848000	Enhancers	Fetal Intestine Large	intestine
48	chr17:44847400-44848200	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr17:44847400-44848200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr17:44847400-44848200	Bivalent Enhancer	Fetal Stomach	stomach

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