Variant report

Variant	rs273265
Chromosome Location	chr19:18284336-18284337
allele	A/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	RUNX3	chr19:18283735-18285484	GM12878	blood:	n/a	n/a
2	EP300	chr19:18283841-18284799	GM12878	blood:	n/a	chr19:18284463-18284479
3	BCLAF1	chr19:18284153-18285439	GM12878	blood:	n/a	chr19:18284613-18284626
4	POLR2A	chr19:18283739-18285887	GM12878	blood:	n/a	n/a
5	EBF1	chr19:18283534-18285324	GM12878	blood:	n/a	chr19:18284013-18284026
6	SP1	chr19:18283730-18285281	GM12878	blood:	n/a	chr19:18283855-18283867 chr19:18284568-18284582 chr19:18284218-18284232 chr19:18283856-18283866 chr19:18284477-18284491 chr19:18284573-18284582 chr19:18283855-18283867 chr19:18284480-18284491 chr19:18283786-18283796 chr19:18283856-18283870 chr19:18283926-18283935 chr19:18284571-18284583 chr19:18283857-18283866 chr19:18284507-18284518 chr19:18284539-18284549 chr19:18284571-18284583 chr19:18283786-18283800
7	ZNF263	chr19:18284230-18284805	HEK293-T-REx	kidney:	n/a	n/a
8	POLR2A	chr19:18284262-18284895	U87	brain:	n/a	n/a
9	POLR2A	chr19:18283906-18285468	GM12892	blood:	n/a	n/a
10	POLR2A	chr19:18284052-18284894	HL-60	blood:	n/a	n/a
11	TEAD4	chr19:18284304-18284779	K562	blood:	n/a	n/a
12	HCFC1	chr19:18283827-18285520	Hela-S3	cervix:	n/a	n/a
13	PAX5	chr19:18283737-18285151	GM12878	blood:	n/a	n/a
14	ELF1	chr19:18283817-18284711	GM12878	blood:	n/a	n/a
15	POLR2A	chr19:18283831-18285547	GM12878	blood:	n/a	n/a
16	USF2	chr19:18283975-18284969	GM12878	blood:	n/a	chr19:18284403-18284416 chr19:18284405-18284414 chr19:18284403-18284414 chr19:18284406-18284415 chr19:18284405-18284414
17	RFX5	chr19:18284316-18285274	Hela-S3	cervix:	n/a	n/a
18	TFAP2C	chr19:18284302-18285420	Hela-S3	cervix:	n/a	n/a
19	MTA3	chr19:18283424-18286187	GM12878	blood:	n/a	n/a
20	BCL3	chr19:18284288-18285112	GM12878	blood:	n/a	chr19:18284613-18284626
21	CHD1	chr19:18283764-18285482	GM12878	blood:	n/a	chr19:18284595-18284602
22	GABPA	chr19:18284137-18284837	K562	blood:	n/a	n/a
23	MAFK	chr19:18284324-18284449	K562	blood:	n/a	n/a
24	CBX3	chr19:18284175-18285547	K562	blood:	n/a	n/a
25	POLR2A	chr19:18281250-18285709	HepG2	liver:	n/a	n/a
26	SIN3A	chr19:18284304-18284858	H1-hESC	embryonic stem cell:	n/a	chr19:18284464-18284473
27	NFIC	chr19:18284166-18285139	ECC-1	luminal epithelium:	n/a	chr19:18284420-18284436 chr19:18284419-18284436
28	MYC	chr19:18284334-18284832	HepG2	liver:	n/a	n/a
29	ATF2	chr19:18283867-18285277	GM12878	blood:	n/a	n/a
30	USF1	chr19:18284204-18284566	GM12878	blood:	n/a	chr19:18284403-18284416 chr19:18284405-18284414 chr19:18284406-18284415 chr19:18284445-18284456 chr19:18284405-18284414
31	RCOR1	chr19:18283605-18285247	GM12878	blood:	n/a	n/a
32	BHLHE40	chr19:18284206-18284788	HepG2	liver:	n/a	chr19:18284403-18284416 chr19:18284405-18284414 chr19:18284406-18284415 chr19:18284405-18284414
33	MAZ	chr19:18284327-18284846	Hela-S3	cervix:	n/a	n/a
34	ZBTB7A	chr19:18283854-18284903	K562	blood:	n/a	n/a
35	POLR2A	chr19:18284258-18284904	HCT-116	colon:	n/a	n/a
36	MAX	chr19:18284193-18285510	ECC-1	luminal epithelium:	n/a	n/a
37	TCF12	chr19:18284310-18284581	H1-hESC	embryonic stem cell:	n/a	n/a
38	ELK1	chr19:18284272-18284723	Hela-S3	cervix:	n/a	n/a
39	POLR2A	chr19:18284205-18285448	K562	blood:	n/a	n/a
40	E2F6	chr19:18284298-18284989	K562	blood:	n/a	chr19:18284595-18284602
41	MAZ	chr19:18283781-18285365	GM12878	blood:	n/a	n/a
42	EP300	chr19:18284069-18285083	ECC-1	luminal epithelium:	n/a	chr19:18284463-18284479
43	RELA	chr19:18283794-18285414	GM19099	blood:	n/a	n/a
44	RCOR1	chr19:18284302-18284778	HepG2	liver:	n/a	n/a
45	NFIC	chr19:18284328-18284717	HepG2	liver:	n/a	chr19:18284420-18284436 chr19:18284419-18284436
46	POLR2A	chr19:18284076-18286311	GM12878	blood:	n/a	n/a
47	POLR2A	chr19:18284173-18284834	HCT-116	colon:	n/a	n/a
48	NR2F2	chr19:18284295-18284807	K562	blood:	n/a	n/a
49	BHLHE40	chr19:18284325-18284553	A549	lung:	n/a	chr19:18284403-18284416 chr19:18284405-18284414 chr19:18284406-18284415 chr19:18284405-18284414
50	USF1	chr19:18284304-18284540	HepG2	liver:	n/a	chr19:18284403-18284416 chr19:18284405-18284414 chr19:18284406-18284415 chr19:18284445-18284456 chr19:18284405-18284414

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:18284321-18284371	Hela-S3	cervix:	n/a
2	chr19:18284321-18284371	SAEC	small airway:	n/a
3	chr19:18284321-18284371	SKMC	muscle:	n/a
4	chr19:18284321-18284371	HEK293	kidney:	embryo
5	chr19:18284321-18284371	HCT-116	colon:	n/a
6	chr19:18284321-18284371	RPTEC	kidney:	n/a
7	chr19:18284321-18284371	GM19239	blood:	n/a
8	chr19:18284321-18284371	HRCEpiC	kidney:	n/a
9	chr19:18284321-18284371	AG04450	lung:	fetal
10	chr19:18284321-18284371	PFSK-1	brain:	n/a
11	chr19:18284321-18284371	LNCaP	prostate:	n/a
12	chr19:18284321-18284371	PANC-1	pancreas:	n/a
13	chr19:18284321-18284371	NHDF-neo	bronchial:	n/a
14	chr19:18284321-18284371	AG09319	gingival:	n/a
15	chr19:18284321-18284371	HRPEpiC	eye:	n/a
16	chr19:18284321-18284371	H1-hESC	embryonic stem cell:	embryo
17	chr19:18284321-18284371	ProgFib	skin:	n/a
18	chr19:18284321-18284371	GM06990	blood:	n/a
19	chr19:18284321-18284371	HEEpiC	esophagus:	n/a
20	chr19:18284321-18284371	HNPCEpiC	eye:	n/a
21	chr19:18284321-18284371	BJ	skin:	n/a
22	chr19:18284321-18284371	NHBE	bronchial:	n/a
23	chr19:18284321-18284371	ECC-1	luminal epithelium:	n/a
24	chr19:18284321-18284371	U87	brain:	n/a
25	chr19:18284321-18284371	HCM	heart:	n/a
26	chr19:18284321-18284371	T-47D	breast:	n/a
27	chr19:18284321-18284371	HAEpiC	amniotic membrane:	n/a
28	chr19:18284321-18284371	HepG2	liver:	n/a
29	chr19:18284321-18284371	HCF	heart:	n/a
30	chr19:18284321-18284371	MCF-7	breast:	n/a
31	chr19:18284321-18284371	ovcar-3	ovarian:	n/a
32	chr19:18284321-18284371	PrEC	prostate:	n/a
33	chr19:18284321-18284371	GM12878	blood:	n/a
34	chr19:18284321-18284371	HMEC	breast:	n/a
35	chr19:18284321-18284371	AG04449	skin:	fetal
36	chr19:18284321-18284371	SK-N-SH_RA	brain:	n/a
37	chr19:18284321-18284371	Jurkat	blood:	n/a
38	chr19:18284321-18284371	HL-60	blood:	n/a
39	chr19:18284321-18284371	Caco-2	colon:	n/a
40	chr19:18284321-18284371	K562	blood:	n/a
41	chr19:18284321-18284371	HCPEpiC	choroid plexus:	n/a
42	chr19:18284321-18284371	Hepatocyte	liver:	n/a
43	chr19:18284321-18284371	BE2_C	brain:	n/a
44	chr19:18284321-18284371	AG10803	skin:	n/a
45	chr19:18284321-18284371	NT2-D1	testis:	n/a
46	chr19:18284321-18284371	IMR90	lung:	fetal
47	chr19:18284321-18284371	NH-A	brain:	n/a
48	chr19:18284321-18284371	HUVEC	blood vessel:	n/a
49	chr19:18284321-18284371	AG09309	skin:	n/a
50	chr19:18284321-18284371	HRE	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:18283376..18285047-chr19:18391434..18393918,2	K562	blood:
2	chr19:18234040..18236524-chr19:18282001..18284422,2	K562	blood:
3	chr19:18283035..18288338-chr19:18301660..18307351,8	K562	blood:
4	chr19:18270841..18274089-chr19:18281381..18284533,5	MCF-7	breast:
5	chr19:18270258..18275351-chr19:18277257..18287386,21	K562	blood:
6	chr19:18253149..18256511-chr19:18283313..18285287,3	K562	blood:
7	chr19:18282901..18285514-chr19:18334924..18337003,2	K562	blood:
8	chr1:28973733..28975604-chr19:18282504..18285384,2	K562	blood:
9	chr19:18278323..18281380-chr19:18281484..18284654,3	MCF-7	breast:
10	chr19:18270372..18276469-chr19:18282239..18286487,12	K562	blood:
11	chr19:18282952..18288338-chr19:18301660..18306832,7	K562	blood:
12	chr19:18260584..18267400-chr19:18276077..18285960,14	MCF-7	breast:
13	chr19:18277547..18280046-chr19:18281617..18284436,4	K562	blood:
14	chr19:18275011..18277551-chr19:18282905..18285760,2	MCF-7	breast:
15	chr19:18284325..18285153-chr9:103115057..103115842,2	HCT-116	colon:

Variant related genes	Relation type
IFI30	TF binding region
IFI30	CpG island
ENSG00000099308	Chromatin interaction
ENSG00000268173	Chromatin interaction
ENSG00000267959	Chromatin interaction
ENSG00000105650	Chromatin interaction
ENSG00000105647	Chromatin interaction
ENSG00000269145	Chromatin interaction
ENSG00000136891	Chromatin interaction
ENSG00000270103	Chromatin interaction
ENSG00000130522	Chromatin interaction
ENSG00000254858	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs1045747	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2241090	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs273266	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2921	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4808118	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4808757	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4808758	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6512247	0.85[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs7248971	0.89[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs7259445	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72999501	0.86[AFR][1000 genomes]
rs73001407	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs887945	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1055932	chr19:17923918-18369944	Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
2	nsv543923	chr19:17923918-18369944	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS Bivalent Enhancer Flanking 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 target site	109 gene(s)	inside rSNPs	diseases
3	nsv532614	chr19:18033043-18573963	Flanking Active TSS Enhancers Active TSS Genic enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	204 gene(s)	inside rSNPs	diseases
4	esv1837595	chr19:18085428-18393682	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	147 gene(s)	inside rSNPs	diseases
5	nsv833773	chr19:18152971-18302988	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
6	nsv911241	chr19:18193191-18304700	Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
7	nsv911242	chr19:18201757-18304700	Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
8	nsv911244	chr19:18206681-18304700	Strong transcription Flanking Active TSS Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
9	nsv911245	chr19:18206681-18338101	Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
10	nsv833774	chr19:18213761-18295329	Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
11	nsv833775	chr19:18213761-18390074	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
12	nsv911247	chr19:18224729-18288069	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
13	nsv911248	chr19:18224729-18338101	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
14	nsv911249	chr19:18224729-18375846	Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
15	nsv911250	chr19:18224729-18376522	Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
16	nsv911251	chr19:18224729-18422364	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
17	nsv911252	chr19:18234588-18338101	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
18	nsv911253	chr19:18240127-18418044	Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
19	nsv916325	chr19:18244780-18534927	Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	167 gene(s)	inside rSNPs	diseases
20	nsv911254	chr19:18248146-18310678	Enhancers Bivalent/Poised TSS Strong transcription Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
21	nsv911256	chr19:18255359-18338101	Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18272800-18284600	Weak transcription	Small Intestine	intestine
2	chr19:18277000-18284400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr19:18277000-18284600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr19:18277400-18284400	Weak transcription	Psoas Muscle	Psoas
5	chr19:18277400-18284400	Weak transcription	HMEC	breast
6	chr19:18277400-18284600	Weak transcription	Fetal Kidney	kidney
7	chr19:18278400-18284400	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr19:18278600-18284400	Weak transcription	Primary T cells from cord blood	blood
9	chr19:18279800-18284400	Weak transcription	HUVEC	blood vessel
10	chr19:18279800-18284600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr19:18280400-18284600	Weak transcription	Aorta	Aorta
12	chr19:18280400-18284600	Weak transcription	Fetal Lung	lung
13	chr19:18280600-18284400	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr19:18280600-18284400	Weak transcription	Esophagus	oesophagus
15	chr19:18281000-18284400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr19:18281400-18284600	Enhancers	Spleen	Spleen
17	chr19:18282000-18284600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr19:18282400-18284400	Enhancers	Left Ventricle	heart
19	chr19:18282400-18284600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
20	chr19:18282400-18284800	Enhancers	Fetal Heart	heart
21	chr19:18282600-18284400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr19:18282800-18284400	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr19:18283400-18284600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
24	chr19:18283600-18284600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
25	chr19:18283800-18284400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
26	chr19:18283800-18284400	Enhancers	Right Ventricle	heart
27	chr19:18283800-18284600	Flanking Active TSS	GM12878-XiMat	blood
28	chr19:18284000-18284400	Enhancers	H1 Cell Line	embryonic stem cell
29	chr19:18284000-18284400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr19:18284000-18284400	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr19:18284000-18284400	Bivalent Enhancer	Fetal Muscle Leg	muscle
32	chr19:18284000-18284400	Enhancers	Pancreas	Pancrea
33	chr19:18284000-18284600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr19:18284000-18284600	Enhancers	Primary T killer memory cells from peripheral blood	blood
35	chr19:18284000-18284600	Enhancers	Sigmoid Colon	Sigmoid Colon
36	chr19:18284000-18284600	Flanking Active TSS	Osteobl	bone
37	chr19:18284000-18285000	Active TSS	Primary T regulatory cells fromperipheralblood	blood
38	chr19:18284000-18285200	Bivalent Enhancer	Fetal Brain Male	brain
39	chr19:18284000-18286000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr19:18284200-18284400	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr19:18284200-18284400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr19:18284200-18284400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
43	chr19:18284200-18284400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
44	chr19:18284200-18284400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr19:18284200-18284400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr19:18284200-18284400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
47	chr19:18284200-18284400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
48	chr19:18284200-18284400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
49	chr19:18284200-18284400	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr19:18284200-18284400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin

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