Variant report

Variant	rs56034325
Chromosome Location	chr7:97841318-97841319
allele	C/T
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	REST	chr7:97840985-97841411	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:97841106-97841413	HepG2	liver:	n/a	n/a
3	MBD4	chr7:97840995-97841414	HepG2	liver:	n/a	n/a
4	MAX	chr7:97840642-97841349	K562	blood:	n/a	chr7:97841309-97841318 chr7:97841308-97841317 chr7:97840955-97840965
5	MYBL2	chr7:97840952-97841530	HepG2	liver:	n/a	n/a
6	MYC	chr7:97840887-97841433	HepG2	liver:	n/a	chr7:97841309-97841318 chr7:97841308-97841317 chr7:97840955-97840965
7	ZBTB7A	chr7:97841105-97841498	HepG2	liver:	n/a	chr7:97841190-97841199
8	CHD2	chr7:97840957-97841477	HepG2	liver:	n/a	n/a
9	FOSL2	chr7:97840900-97841588	HepG2	liver:	n/a	chr7:97841308-97841318 chr7:97841307-97841319 chr7:97841309-97841317 chr7:97841309-97841318 chr7:97841279-97841290 chr7:97841305-97841316 chr7:97841308-97841317 chr7:97841310-97841317
10	SP1	chr7:97841001-97841539	HepG2	liver:	n/a	chr7:97841316-97841329
11	RFX5	chr7:97841222-97841334	HepG2	liver:	n/a	n/a
12	POLR2A	chr7:97840747-97841605	HepG2	liver:	n/a	n/a
13	POLR2A	chr7:97841047-97842554	Hela-S3	cervix:	n/a	n/a
14	POLR2A	chr7:97841313-97841360	K562	blood:	n/a	n/a
15	JUND	chr7:97840958-97841592	MCF-7	breast:	n/a	chr7:97841308-97841318 chr7:97841307-97841319 chr7:97841309-97841317 chr7:97841309-97841318 chr7:97841279-97841290 chr7:97841307-97841318 chr7:97841305-97841316 chr7:97841308-97841317 chr7:97841310-97841317
16	POLR2A	chr7:97840610-97841390	HepG2	liver:	n/a	n/a
17	BHLHE40	chr7:97840739-97841503	HepG2	liver:	n/a	n/a
18	JUND	chr7:97841060-97841478	HepG2	liver:	n/a	chr7:97841308-97841318 chr7:97841307-97841319 chr7:97841309-97841317 chr7:97841309-97841318 chr7:97841279-97841290 chr7:97841307-97841318 chr7:97841305-97841316 chr7:97841308-97841317 chr7:97841310-97841317
19	JUND	chr7:97841109-97841477	K562	blood:	n/a	chr7:97841308-97841318 chr7:97841307-97841319 chr7:97841309-97841317 chr7:97841309-97841318 chr7:97841279-97841290 chr7:97841307-97841318 chr7:97841305-97841316 chr7:97841308-97841317 chr7:97841310-97841317
20	EP300	chr7:97840966-97841484	HepG2	liver:	n/a	chr7:97841309-97841318 chr7:97841308-97841317
21	JUND	chr7:97841085-97841476	HepG2	liver:	n/a	chr7:97841308-97841318 chr7:97841307-97841319 chr7:97841309-97841317 chr7:97841309-97841318 chr7:97841279-97841290 chr7:97841307-97841318 chr7:97841305-97841316 chr7:97841308-97841317 chr7:97841310-97841317
22	EGR1	chr7:97840946-97841568	K562	blood:	n/a	chr7:97841382-97841391 chr7:97841378-97841393 chr7:97841380-97841391 chr7:97841379-97841392 chr7:97841379-97841393 chr7:97841379-97841392
23	RCOR1	chr7:97841199-97841387	K562	blood:	n/a	n/a
24	NR2F2	chr7:97840726-97841594	MCF-7	breast:	n/a	chr7:97841232-97841247 chr7:97841228-97841243
25	HDAC2	chr7:97840644-97841559	HepG2	liver:	n/a	n/a
26	NR2F2	chr7:97841020-97841434	K562	blood:	n/a	chr7:97841232-97841247 chr7:97841228-97841243
27	TBP	chr7:97840993-97841389	HepG2	liver:	n/a	n/a
28	RCOR1	chr7:97841004-97841530	HepG2	liver:	n/a	n/a
29	FOSL2	chr7:97840959-97841573	HepG2	liver:	n/a	chr7:97841308-97841318 chr7:97841307-97841319 chr7:97841309-97841317 chr7:97841309-97841318 chr7:97841279-97841290 chr7:97841305-97841316 chr7:97841308-97841317 chr7:97841310-97841317
30	JUND	chr7:97841120-97841482	H1-hESC	embryonic stem cell:	n/a	chr7:97841308-97841318 chr7:97841307-97841319 chr7:97841309-97841317 chr7:97841309-97841318 chr7:97841279-97841290 chr7:97841307-97841318 chr7:97841305-97841316 chr7:97841308-97841317 chr7:97841310-97841317
31	HNF4G	chr7:97840952-97841520	HepG2	liver:	n/a	chr7:97841230-97841243 chr7:97841226-97841248 chr7:97841231-97841243 chr7:97841228-97841246 chr7:97841231-97841243 chr7:97841000-97841014 chr7:97841231-97841244 chr7:97841230-97841244 chr7:97841230-97841243 chr7:97841001-97841014 chr7:97841228-97841243 chr7:97841235-97841247 chr7:97841230-97841243
32	FOS	chr7:97841251-97841417	MCF10A-Er-Src	breast:	n/a	chr7:97841308-97841318 chr7:97841307-97841319 chr7:97841309-97841317 chr7:97841309-97841318 chr7:97841279-97841290 chr7:97841305-97841316 chr7:97841308-97841317 chr7:97841310-97841317
33	EP300	chr7:97840895-97841575	HepG2	liver:	n/a	chr7:97841309-97841318 chr7:97841308-97841317
34	EGR1	chr7:97840917-97841582	MCF-7	breast:	n/a	chr7:97841382-97841391 chr7:97841378-97841393 chr7:97841380-97841391 chr7:97841379-97841392 chr7:97841379-97841393 chr7:97841379-97841392
35	HNF4A	chr7:97840989-97841470	HepG2	liver:	n/a	chr7:97841230-97841243 chr7:97841226-97841248 chr7:97841231-97841243 chr7:97841228-97841246 chr7:97841231-97841243 chr7:97841000-97841014 chr7:97841231-97841244 chr7:97841230-97841244 chr7:97841229-97841244 chr7:97841230-97841243 chr7:97841001-97841014 chr7:97841235-97841247 chr7:97841230-97841243
36	FOSL1	chr7:97841101-97841449	K562	blood:	n/a	chr7:97841307-97841318 chr7:97841308-97841318 chr7:97841307-97841319 chr7:97841309-97841317 chr7:97841309-97841318 chr7:97841279-97841290 chr7:97841305-97841316 chr7:97841308-97841317 chr7:97841310-97841317
37	YY1	chr7:97840928-97841382	HepG2	liver:	n/a	n/a
38	FOSL1	chr7:97841064-97841466	K562	blood:	n/a	chr7:97841307-97841318 chr7:97841308-97841318 chr7:97841307-97841319 chr7:97841309-97841317 chr7:97841309-97841318 chr7:97841279-97841290 chr7:97841305-97841316 chr7:97841308-97841317 chr7:97841310-97841317
39	NFIC	chr7:97841072-97841566	HepG2	liver:	n/a	n/a
40	RXRA	chr7:97841041-97841573	HepG2	liver:	n/a	chr7:97841230-97841243 chr7:97841308-97841317 chr7:97841229-97841245 chr7:97841230-97841243 chr7:97841235-97841244 chr7:97841227-97841247 chr7:97841319-97841333 chr7:97841230-97841243 chr7:97841309-97841318
41	TEAD4	chr7:97840983-97841549	HepG2	liver:	n/a	n/a
42	EGR1	chr7:97840998-97841531	K562	blood:	n/a	chr7:97841382-97841391 chr7:97841378-97841393 chr7:97841380-97841391 chr7:97841379-97841392 chr7:97841379-97841393 chr7:97841379-97841392
43	NR2C2	chr7:97840911-97841414	HepG2	liver:	n/a	chr7:97841230-97841243 chr7:97841003-97841012 chr7:97841228-97841243 chr7:97841001-97841014
44	JUN	chr7:97841133-97841471	HepG2	liver:	n/a	chr7:97841308-97841318 chr7:97841307-97841319 chr7:97841309-97841317 chr7:97841309-97841318 chr7:97841279-97841290 chr7:97841305-97841316 chr7:97841308-97841317 chr7:97841310-97841317
45	MXI1	chr7:97840907-97841648	HepG2	liver:	n/a	chr7:97840957-97840966
46	FOSL2	chr7:97841053-97841512	MCF-7	breast:	n/a	chr7:97841308-97841318 chr7:97841307-97841319 chr7:97841309-97841317 chr7:97841309-97841318 chr7:97841279-97841290 chr7:97841305-97841316 chr7:97841308-97841317 chr7:97841310-97841317
47	MYBL2	chr7:97840892-97841563	HepG2	liver:	n/a	n/a
48	MAX	chr7:97840715-97841451	HepG2	liver:	n/a	chr7:97841309-97841318 chr7:97841308-97841317 chr7:97840955-97840965
49	ZBTB7A	chr7:97841095-97841341	K562	blood:	n/a	chr7:97841190-97841199
50	NR2F2	chr7:97840894-97841602	HepG2	liver:	n/a	chr7:97841232-97841247 chr7:97841228-97841243

No.	Distal block	Cell Line	Cell type
1	chr7:97840173..97842487-chr7:97845725..97848039,2	MCF-7	breast:
2	chr10:8099641..8101523-chr7:97840811..97843007,2	MCF-7	breast:
3	chr7:97841230..97842751-chr7:97851743..97853660,2	K562	blood:
4	chr7:97840856..97842377-chr7:97845637..97848224,2	MCF-7	breast:
5	chr7:97839660..97842920-chr7:97872632..97874833,3	K562	blood:

Variant related genes	Relation type
BHLHA15	TF binding region
ENSG00000205356	Chromatin interaction
ENSG00000107485	Chromatin interaction

Extended variants
information (count: 46 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs1039057	0.96[EUR][1000 genomes]
rs11761896	0.95[EUR][1000 genomes]
rs11762771	0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11762810	0.84[EUR][1000 genomes]
rs11768678	0.95[EUR][1000 genomes]
rs11772060	0.96[EUR][1000 genomes]
rs11773169	0.96[EUR][1000 genomes]
rs1532380	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17169325	0.95[EUR][1000 genomes]
rs2394824	0.95[EUR][1000 genomes]
rs4729404	0.95[EUR][1000 genomes]
rs4729408	0.95[EUR][1000 genomes]
rs55761857	0.95[EUR][1000 genomes]
rs55765204	0.90[EUR][1000 genomes]
rs56006208	0.93[EUR][1000 genomes]
rs56088922	0.95[EUR][1000 genomes]
rs56174823	0.89[EUR][1000 genomes]
rs56389625	0.95[EUR][1000 genomes]
rs58911561	0.96[EUR][1000 genomes]
rs62479768	0.88[EUR][1000 genomes]
rs62479773	0.89[EUR][1000 genomes]
rs62479795	0.95[EUR][1000 genomes]
rs62479797	0.95[EUR][1000 genomes]
rs73149199	0.82[EUR][1000 genomes]
rs740208	0.82[EUR][1000 genomes]
rs884897	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1031371	chr7:97312452-98070538	Flanking Active TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	esv3500384	chr7:97527787-98015382	Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	36 gene(s)	inside rSNPs	diseases
3	esv3500386	chr7:97527787-98015382	Bivalent Enhancer Flanking Active TSS Strong transcription Enhancers Genic enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	36 gene(s)	inside rSNPs	diseases
4	nsv1017481	chr7:97597641-98041043	Active TSS Weak transcription Flanking Active TSS Genic enhancers Strong transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
5	nsv539031	chr7:97597641-98041043	Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Bivalent Enhancer 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	32 gene(s)	inside rSNPs	diseases
6	nsv1019531	chr7:97653880-98034129	Weak transcription Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
7	nsv539032	chr7:97653880-98034129	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
8	esv1816676	chr7:97676259-97868033	Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
9	nsv831066	chr7:97726879-97890550	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers 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	10 gene(s)	inside rSNPs	diseases
10	nsv1033029	chr7:97773232-98017992	Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
11	nsv539033	chr7:97773232-98017992	Genic enhancers Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
12	nsv888760	chr7:97816327-97965016	Weak transcription Bivalent/Poised TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
13	nsv888761	chr7:97829492-97844578	Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
14	nsv888762	chr7:97829492-97853184	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS 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	5 gene(s)	inside rSNPs	diseases
15	nsv888763	chr7:97829492-97866291	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
16	nsv888764	chr7:97832628-97844578	Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
17	nsv888765	chr7:97834386-97853184	Bivalent Enhancer Enhancers Strong transcription Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
18	esv3355961	chr7:97839041-97842189	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
19	esv3424111	chr7:97839316-97841814	Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
20	esv3341216	chr7:97839416-97841614	Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs56034325	DKFZP434B0335	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:95 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:97823000-97851000	Weak transcription	HSMMtube	muscle
2	chr7:97825200-97851000	Weak transcription	Fetal Lung	lung
3	chr7:97836000-97851000	Weak transcription	NHLF	lung
4	chr7:97836600-97846200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr7:97836600-97847200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr7:97836800-97857200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr7:97837000-97846600	Weak transcription	Dnd41	blood
8	chr7:97839200-97844800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr7:97839200-97851000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr7:97839400-97841400	Active TSS	H9 Cell Line	embryonic stem cell
11	chr7:97839600-97841400	Active TSS	HUES64 Cell Line	embryonic stem cell
12	chr7:97839800-97841400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr7:97839800-97841400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr7:97839800-97841400	Enhancers	Fetal Brain Male	brain
15	chr7:97839800-97844400	Active TSS	Pancreatic Islets	Pancreatic Islet
16	chr7:97840000-97841400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
17	chr7:97840200-97841400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
18	chr7:97840200-97841800	Active TSS	Pancreas	Pancrea
19	chr7:97840200-97846000	Weak transcription	Brain Hippocampus Middle	brain
20	chr7:97840200-97847000	Weak transcription	Brain Cingulate Gyrus	brain
21	chr7:97840200-97847200	Weak transcription	Brain Anterior Caudate	brain
22	chr7:97840200-97847200	Weak transcription	Brain Substantia Nigra	brain
23	chr7:97840200-97851000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr7:97840400-97845600	Weak transcription	Small Intestine	intestine
25	chr7:97840400-97847000	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr7:97840400-97852800	Weak transcription	Brain Angular Gyrus	brain
27	chr7:97840800-97841400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
28	chr7:97840800-97841400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
29	chr7:97840800-97841400	Enhancers	Esophagus	oesophagus
30	chr7:97840800-97841600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
31	chr7:97840800-97841600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr7:97840800-97842400	Active TSS	Gastric	stomach
33	chr7:97840800-97844800	Weak transcription	Aorta	Aorta
34	chr7:97841000-97841400	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr7:97841000-97841400	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr7:97841000-97841400	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
37	chr7:97841000-97841400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
38	chr7:97841000-97841400	Enhancers	Primary T helper naive cells from peripheral blood	blood
39	chr7:97841000-97841400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr7:97841000-97841400	Enhancers	Primary T killer memory cells from peripheral blood	blood
41	chr7:97841000-97841400	Flanking Active TSS	Liver	Liver
42	chr7:97841000-97841400	Flanking Active TSS	Colonic Mucosa	Colon
43	chr7:97841000-97841400	Flanking Active TSS	Duodenum Mucosa	Duodenum
44	chr7:97841000-97841400	Flanking Active TSS	Fetal Intestine Large	intestine
45	chr7:97841000-97841400	Flanking Active TSS	Fetal Intestine Small	intestine
46	chr7:97841000-97841400	Enhancers	Lung	lung
47	chr7:97841000-97841400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
48	chr7:97841000-97841400	Enhancers	Right Ventricle	heart
49	chr7:97841000-97841400	Flanking Active TSS	GM12878-XiMat	blood
50	chr7:97841000-97841400	Flanking Active TSS	K562	blood

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