Variant report

Variant	rs56069762
Chromosome Location	chr14:105560437-105560438
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	NRF1	chr14:105559146-105560604	SK-N-SH	brain:	n/a	chr14:105559638-105559649 chr14:105559640-105559649 chr14:105559598-105559607 chr14:105559638-105559652 chr14:105559635-105559649 chr14:105559574-105559583
2	RUNX3	chr14:105559892-105560480	GM12878	blood:	n/a	chr14:105560286-105560303
3	PBX3	chr14:105559730-105560683	A549	lung:	n/a	n/a
4	TCF12	chr14:105559888-105560597	ECC-1	luminal epithelium:	n/a	chr14:105560562-105560572
5	SP1	chr14:105559846-105560696	A549	lung:	n/a	chr14:105560338-105560350 chr14:105560339-105560348 chr14:105560340-105560349 chr14:105560338-105560350 chr14:105560263-105560275 chr14:105560339-105560349 chr14:105560340-105560349 chr14:105560430-105560444 chr14:105560263-105560275
6	POLR2A	chr14:105557226-105561146	A549	lung:	n/a	n/a
7	STAT3	chr14:105559978-105560494	MCF10A-Er-Src	breast:	n/a	chr14:105560330-105560342 chr14:105560060-105560072 chr14:105560315-105560326
8	POLR2A	chr14:105559482-105560477	MCF10A-Er-Src	breast:	n/a	n/a
9	MAX	chr14:105559856-105560679	ECC-1	luminal epithelium:	n/a	n/a
10	TCF12	chr14:105552661-105561002	A549	lung:	n/a	chr14:105555506-105555515 chr14:105554733-105554741 chr14:105554099-105554109 chr14:105560562-105560572 chr14:105558705-105558715 chr14:105556711-105556721 chr14:105560974-105560982 chr14:105558506-105558516 chr14:105555994-105556004 chr14:105558328-105558335 chr14:105556609-105556616 chr14:105556879-105556889 chr14:105556900-105556910 chr14:105558295-105558305 chr14:105557507-105557514
11	RCOR1	chr14:105560030-105560460	GM12878	blood:	n/a	n/a
12	POLR2A	chr14:105560012-105560751	A549	lung:	n/a	n/a
13	CTCF	chr14:105559771-105560736	A549	lung:	n/a	chr14:105560394-105560407 chr14:105560586-105560595
14	SP1	chr14:105559819-105560701	A549	lung:	n/a	chr14:105560338-105560350 chr14:105560339-105560348 chr14:105560340-105560349 chr14:105560338-105560350 chr14:105560263-105560275 chr14:105560339-105560349 chr14:105560340-105560349 chr14:105560430-105560444 chr14:105560263-105560275
15	MAX	chr14:105559967-105560577	SK-N-SH	brain:	n/a	n/a
16	MYC	chr14:105560264-105560464	MCF10A-Er-Src	breast:	n/a	n/a
17	FOXA2	chr14:105559872-105560510	A549	lung:	n/a	n/a
18	ZNF143	chr14:105560022-105560490	GM12878	blood:	n/a	chr14:105560328-105560347 chr14:105560148-105560166
19	STAT3	chr14:105560133-105560497	MCF10A-Er-Src	breast:	n/a	chr14:105560330-105560342 chr14:105560315-105560326
20	NFIC	chr14:105559909-105560599	ECC-1	luminal epithelium:	n/a	n/a
21	POLR2A	chr14:105557763-105560968	A549	lung:	n/a	n/a
22	POLR2A	chr14:105559905-105560765	SK-N-MC	brain:	n/a	n/a
23	TAF1	chr14:105559861-105560663	A549	lung:	n/a	n/a
24	REST	chr14:105559896-105560639	A549	lung:	n/a	chr14:105559947-105559960
25	POLR2A	chr14:105557708-105560589	HCT-116	colon:	n/a	n/a
26	POLR2A	chr14:105557554-105560595	A549	lung:	n/a	n/a
27	RAD21	chr14:105559891-105560620	ECC-1	luminal epithelium:	n/a	chr14:105560556-105560569 chr14:105560564-105560578
28	YY1	chr14:105560097-105560443	H1-hESC	embryonic stem cell:	n/a	chr14:105560261-105560275
29	PAX5	chr14:105559862-105560458	GM12892	blood:	n/a	n/a
30	MAX	chr14:105559976-105560614	H1-hESC	embryonic stem cell:	n/a	n/a
31	REST	chr14:105559879-105560750	A549	lung:	n/a	chr14:105560646-105560659 chr14:105559947-105559960
32	CTCF	chr14:105560360-105560510	HRE	kidney:	n/a	chr14:105560394-105560407
33	POLR2A	chr14:105559828-105560636	HCT-116	colon:	n/a	n/a
34	EP300	chr14:105556632-105561231	ECC-1	luminal epithelium:	n/a	chr14:105559405-105559421 chr14:105557498-105557514 chr14:105559121-105559137 chr14:105557385-105557401 chr14:105556882-105556898 chr14:105559636-105559652 chr14:105558269-105558285
35	ZNF263	chr14:105560151-105561188	HEK293-T-REx	kidney:	n/a	chr14:105560830-105560851 chr14:105560857-105560878
36	MAX	chr14:105559984-105560499	H1-hESC	embryonic stem cell:	n/a	n/a
37	ZBTB7A	chr14:105556759-105561147	ECC-1	luminal epithelium:	n/a	chr14:105559442-105559450 chr14:105557003-105557012
38	ELF1	chr14:105559811-105560649	GM12878	blood:	n/a	chr14:105560337-105560349 chr14:105560620-105560632
39	POLR2A	chr14:105559502-105560529	K562	blood:	n/a	n/a
40	YY1	chr14:105559940-105560479	A549	lung:	n/a	chr14:105559941-105559955 chr14:105559944-105559955 chr14:105559981-105559990 chr14:105560261-105560275
41	E2F4	chr14:105560212-105560494	MCF10A-Er-Src	breast:	n/a	chr14:105560324-105560336
42	ELF1	chr14:105560117-105560467	A549	lung:	n/a	chr14:105560337-105560349
43	KAP1	chr14:105560047-105560601	U2OS	brain:	n/a	n/a
44	USF2	chr14:105560288-105560701	H1-hESC	embryonic stem cell:	n/a	chr14:105560390-105560406
45	ZBTB7A	chr14:105558922-105560907	ECC-1	luminal epithelium:	n/a	chr14:105559442-105559450
46	EGR1	chr14:105559165-105560966	HCT-116	colon:	n/a	chr14:105560432-105560445 chr14:105560323-105560333 chr14:105560259-105560272 chr14:105560280-105560294 chr14:105560174-105560187 chr14:105559297-105559307 chr14:105560842-105560852 chr14:105560279-105560292 chr14:105560260-105560274 chr14:105559639-105559648 chr14:105559296-105559306
47	CREB1	chr14:105559968-105560511	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr14:105559997-105560496	GM12878	blood:	n/a	n/a
49	POLR2A	chr14:105557741-105560748	ECC-1	luminal epithelium:	n/a	n/a
50	CTCF	chr14:105559983-105560494	K562	blood:	n/a	chr14:105560394-105560407

Variant related genes	Relation type
ENSG00000257556	TF binding region

Extended variants
information (count: 57 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10129625	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10130501	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10130930	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10144185	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11621606	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12435117	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12885313	0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12885315	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12885324	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12886669	0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12886677	0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12896149	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs34235655	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs35133619	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs36171475	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4357873	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4377097	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6576074	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7150778	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7155121	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7156642	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7156965	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7157947	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7158479	0.83[AMR][1000 genomes]
rs7158905	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7159054	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7160811	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7161438	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs8003024	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs8003920	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs8004326	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs8006160	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs8014250	0.80[EUR][1000 genomes]
rs8015942	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs8018607	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9324081	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9743945	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][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	esv1828345	chr14:105100787-105803170	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS 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 miRNA target site	165 gene(s)	inside rSNPs	diseases
2	nsv542225	chr14:105133688-105803170	Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
3	nsv542227	chr14:105157572-105803170	Enhancers Flanking Active TSS Genic enhancers Weak transcription Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	147 gene(s)	inside rSNPs	diseases
4	nsv917106	chr14:105339195-105803170	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS 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 miRNA target site	94 gene(s)	inside rSNPs	diseases
5	nsv902421	chr14:105410183-105574843	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Strong 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	73 gene(s)	inside rSNPs	diseases
6	nsv902422	chr14:105420215-105803170	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
7	nsv1052190	chr14:105423761-105722653	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
8	nsv902423	chr14:105430890-105803170	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription Genic enhancers 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 miRNA target site	88 gene(s)	inside rSNPs	diseases
9	nsv1042303	chr14:105435649-105633544	Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers 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
10	nsv456458	chr14:105435649-105690092	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS 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 miRNA target site	77 gene(s)	inside rSNPs	diseases
11	nsv566150	chr14:105435649-105690092	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
12	nsv902424	chr14:105436222-105803170	Genic enhancers Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS 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 miRNA target site	86 gene(s)	inside rSNPs	diseases
13	nsv456459	chr14:105459140-105617891	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
14	nsv566152	chr14:105459140-105617891	Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS 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	55 gene(s)	inside rSNPs	diseases
15	nsv902425	chr14:105463936-105690092	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
16	nsv9175	chr14:105496509-105688941	Enhancers Strong transcription Bivalent/Poised TSS Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
17	nsv902427	chr14:105508577-105585347	Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
18	esv2758369	chr14:105513346-105803170	Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
19	esv2760014	chr14:105513346-105803170	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
20	esv3353199	chr14:105558957-105560855	Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr14:105557800-105561000	Flanking Active TSS	Colonic Mucosa	Colon
2	chr14:105557800-105561000	Flanking Active TSS	HMEC	breast
3	chr14:105558600-105560800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
4	chr14:105559000-105560600	Active TSS	H9 Cell Line	embryonic stem cell
5	chr14:105559000-105560600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr14:105559000-105560800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
7	chr14:105559000-105560800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
8	chr14:105559000-105561200	Flanking Active TSS	Dnd41	blood
9	chr14:105559200-105560600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr14:105559200-105560600	Active TSS	Pancreatic Islets	Pancreatic Islet
11	chr14:105559200-105560600	Bivalent/Poised TSS	Thymus	Thymus
12	chr14:105559200-105560800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
13	chr14:105559200-105560800	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr14:105559200-105560800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr14:105559200-105560800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
16	chr14:105559200-105560800	Active TSS	Brain Inferior Temporal Lobe	brain
17	chr14:105559400-105560600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
18	chr14:105559400-105560600	Active TSS	Brain Angular Gyrus	brain
19	chr14:105559400-105560600	Active TSS	Osteobl	bone
20	chr14:105559400-105560800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr14:105559400-105560800	Active TSS	HSMM	muscle
22	chr14:105559400-105561000	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
23	chr14:105559600-105560600	Bivalent/Poised TSS	Psoas Muscle	Psoas
24	chr14:105559600-105560600	Active TSS	NHLF	lung
25	chr14:105559800-105560600	Flanking Bivalent TSS/Enh	Primary neutrophils fromperipheralblood	blood
26	chr14:105559800-105560600	Flanking Active TSS	Primary hematopoietic stem cells	blood
27	chr14:105559800-105561000	Flanking Active TSS	Spleen	Spleen
28	chr14:105560000-105560600	Flanking Active TSS	Primary B cells from cord blood	blood
29	chr14:105560000-105560600	Flanking Active TSS	Liver	Liver
30	chr14:105560000-105560600	Active TSS	Fetal Kidney	kidney
31	chr14:105560000-105560600	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
32	chr14:105560000-105560800	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr14:105560000-105560800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
34	chr14:105560000-105560800	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
35	chr14:105560000-105560800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr14:105560000-105560800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr14:105560000-105560800	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr14:105560000-105560800	Flanking Active TSS	Adipose Nuclei	Adipose
39	chr14:105560000-105560800	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
40	chr14:105560000-105560800	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
41	chr14:105560000-105560800	Flanking Active TSS	Stomach Smooth Muscle	stomach
42	chr14:105560000-105561000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
43	chr14:105560000-105561200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr14:105560200-105560600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
45	chr14:105560200-105560600	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
46	chr14:105560200-105560600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr14:105560200-105560600	Flanking Bivalent TSS/Enh	Primary mononuclear cells fromperipheralblood	Blood
48	chr14:105560200-105560600	Flanking Active TSS	HepG2	liver
49	chr14:105560200-105560800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr14:105560200-105560800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin

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