Variant report

Variant	rs183371945
Chromosome Location	chr17:37823838-37823839
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	EGR1	chr17:37823656-37824216	K562	blood:	n/a	n/a
2	E2F6	chr17:37823213-37824200	K562	blood:	n/a	chr17:37823412-37823422 chr17:37823830-37823841
3	E2F6	chr17:37823672-37824322	K562	blood:	n/a	chr17:37823830-37823841
4	YY1	chr17:37823679-37825084	K562	blood:	n/a	chr17:37823814-37823823 chr17:37823817-37823826 chr17:37824597-37824616 chr17:37824711-37824725 chr17:37824225-37824239 chr17:37824518-37824532
5	JUN	chr17:37822708-37824178	K562	blood:	n/a	chr17:37823320-37823329 chr17:37823320-37823330 chr17:37823721-37823735
6	MYC	chr17:37823769-37824073	K562	blood:	n/a	n/a
7	POLR2A	chr17:37823556-37825166	K562	blood:	n/a	n/a
8	BHLHE40	chr17:37823768-37824112	K562	blood:	n/a	chr17:37823896-37823912
9	POLR2A	chr17:37823100-37824994	K562	blood:	n/a	n/a
10	IRF1	chr17:37823748-37824041	K562	blood:	n/a	n/a
11	ZBTB7A	chr17:37823027-37825041	K562	blood:	n/a	chr17:37824004-37824012 chr17:37824015-37824026 chr17:37824298-37824305
12	PML	chr17:37823660-37824038	K562	blood:	n/a	n/a
13	NR3C1	chr17:37823815-37824110	A549	lung:	n/a	chr17:37823836-37823850 chr17:37824032-37824049 chr17:37824042-37824051 chr17:37824033-37824050 chr17:37824034-37824048 chr17:37824030-37824051 chr17:37824034-37824048
14	GATA1	chr17:37823373-37824111	PBDE	blood:	n/a	chr17:37823866-37823883 chr17:37823959-37823968
15	TAF1	chr17:37823722-37824173	K562	blood:	n/a	n/a
16	NR3C1	chr17:37823646-37824210	A549	lung:	n/a	chr17:37823836-37823850 chr17:37824032-37824049 chr17:37824042-37824051 chr17:37824033-37824050 chr17:37823793-37823806 chr17:37824034-37824048 chr17:37824030-37824051 chr17:37824034-37824048
17	UBTF	chr17:37823648-37824197	K562	blood:	n/a	n/a
18	RCOR1	chr17:37823151-37825237	K562	blood:	n/a	n/a
19	HCFC1	chr17:37823722-37824096	K562	blood:	n/a	n/a
20	UBTF	chr17:37823641-37825091	K562	blood:	n/a	n/a
21	EP300	chr17:37823689-37824202	K562	blood:	n/a	chr17:37823898-37823907 chr17:37823817-37823826 chr17:37823814-37823823
22	POLR2A	chr17:37819928-37825272	K562	blood:	n/a	n/a
23	TEAD4	chr17:37823676-37824162	K562	blood:	n/a	n/a
24	GATA2	chr17:37823647-37824166	K562	blood:	n/a	chr17:37823866-37823883 chr17:37823959-37823968
25	MYC	chr17:37823239-37825086	K562	blood:	n/a	chr17:37824602-37824611 chr17:37823321-37823330
26	E2F4	chr17:37823635-37824080	K562	blood:	n/a	chr17:37823830-37823841
27	GATA1	chr17:37823750-37824044	PBDEFetal	blood:	n/a	chr17:37823866-37823883 chr17:37823959-37823968
28	GABPA	chr17:37823653-37824217	K562	blood:	n/a	n/a
29	POLR2A	chr17:37823704-37824271	K562	blood:	n/a	n/a
30	MAX	chr17:37823703-37824152	K562	blood:	n/a	n/a
31	HEY1	chr17:37823574-37824200	K562	blood:	n/a	chr17:37823735-37823750
32	CEBPD	chr17:37823653-37824269	K562	blood:	n/a	n/a
33	HDAC2	chr17:37823121-37824141	K562	blood:	n/a	chr17:37823876-37823885
34	EGR1	chr17:37823605-37825268	K562	blood:	n/a	chr17:37824635-37824648 chr17:37825132-37825145 chr17:37824372-37824381 chr17:37824630-37824652 chr17:37824635-37824645 chr17:37825131-37825146 chr17:37824195-37824219
35	YY1	chr17:37823699-37824102	K562	blood:	n/a	chr17:37823814-37823823 chr17:37823817-37823826
36	ZBTB7A	chr17:37822966-37824999	K562	blood:	n/a	chr17:37824004-37824012 chr17:37824015-37824026 chr17:37824298-37824305
37	NR2F2	chr17:37822571-37824231	K562	blood:	n/a	n/a
38	GATA3	chr17:37823771-37824002	SH-SY5Y	brain:	n/a	chr17:37823866-37823883 chr17:37823959-37823968
39	ZBTB7A	chr17:37823808-37825078	ECC-1	luminal epithelium:	n/a	chr17:37824004-37824012 chr17:37824015-37824026 chr17:37824298-37824305
40	GATA1	chr17:37823718-37824132	K562	blood:	n/a	chr17:37823866-37823883 chr17:37823959-37823968
41	POLR2A	chr17:37822690-37824064	K562	blood:	n/a	n/a
42	NR2F2	chr17:37823680-37824087	K562	blood:	n/a	n/a
43	RAD21	chr17:37823710-37823845	K562	blood:	n/a	n/a
44	RCOR1	chr17:37823428-37824009	K562	blood:	n/a	n/a
45	ELF1	chr17:37823611-37824202	K562	blood:	n/a	chr17:37823897-37823909
46	CBX3	chr17:37823704-37824096	K562	blood:	n/a	n/a
47	TAL1	chr17:37823659-37824141	K562	blood:	n/a	chr17:37823866-37823884
48	PML	chr17:37823672-37824093	K562	blood:	n/a	n/a
49	POLR2A	chr17:37823712-37823898	K562	blood:	n/a	n/a
50	CCNT2	chr17:37823497-37824187	K562	blood:	n/a	chr17:37824123-37824132 chr17:37823776-37823785

No.	Distal block	Cell Line	Cell type
1	chr17:37822303..37824126-chr17:37856298..37859081,2	K562	blood:
2	chr17:37820932..37826284-chr17:37838504..37843351,7	K562	blood:
3	chr17:37775807..37781695-chr17:37822673..37828377,10	K562	blood:
4	chr17:37791520..37796368-chr17:37822308..37826994,8	K562	blood:
5	chr17:37821804..37826261-chr17:37885454..37888153,4	K562	blood:
6	chr17:37809503..37812375-chr17:37822536..37826640,4	K562	blood:
7	chr17:37702516..37704166-chr17:37823518..37825070,2	K562	blood:
8	chr17:37777756..37783081-chr17:37819129..37825010,9	K562	blood:

Variant related genes	Relation type
PNMT	TF binding region
ENSG00000131771	Chromatin interaction
ENSG00000141736	Chromatin interaction
ENSG00000167258	Chromatin interaction
ENSG00000141741	Chromatin interaction
ENSG00000131748	Chromatin interaction
ENSG00000161395	Chromatin interaction
ENSG00000214546	Chromatin interaction

Extended variants
information (count: 16 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv932024	chr17:37192290-37850932	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	92 gene(s)	inside rSNPs	diseases
2	esv1825702	chr17:37487168-37876767	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
3	nsv833442	chr17:37692880-37861291	Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
4	nsv908205	chr17:37709422-37830900	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
5	nsv908206	chr17:37709422-37866005	Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
6	nsv908207	chr17:37709422-37922259	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
7	nsv833443	chr17:37725640-37882864	Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
8	nsv457738	chr17:37770005-37831035	Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
9	nsv574991	chr17:37770005-37831035	Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers 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	18 gene(s)	inside rSNPs	diseases
10	nsv516757	chr17:37781849-37834541	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	16 gene(s)	inside rSNPs	diseases
11	esv1792029	chr17:37797757-37886460	Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription 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 miRNA target site	20 gene(s)	inside rSNPs	diseases
12	nsv908213	chr17:37807698-37839493	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases
13	nsv528093	chr17:37814080-37866005	Weak transcription Bivalent Enhancer Enhancers Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
14	nsv908214	chr17:37814224-37861833	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
15	nsv908215	chr17:37818561-37834541	Strong transcription Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases
16	esv3377948	chr17:37823251-37825999	Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:93 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:37819200-37825200	Enhancers	Liver	Liver
2	chr17:37819600-37824200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr17:37820400-37825200	Enhancers	Brain Angular Gyrus	brain
4	chr17:37820600-37824000	Enhancers	HSMMtube	muscle
5	chr17:37821000-37824400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
6	chr17:37821200-37824600	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
7	chr17:37821600-37824000	Bivalent Enhancer	Brain Germinal Matrix	brain
8	chr17:37821600-37824600	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
9	chr17:37821800-37824400	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr17:37821800-37825200	Active TSS	Psoas Muscle	Psoas
11	chr17:37822000-37824400	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
12	chr17:37822000-37824600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr17:37822000-37825200	Enhancers	Lung	lung
14	chr17:37822400-37824000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr17:37822600-37824000	Bivalent Enhancer	Fetal Intestine Small	intestine
16	chr17:37822600-37824000	Enhancers	Ovary	ovary
17	chr17:37822800-37824200	Enhancers	Gastric	stomach
18	chr17:37822800-37824600	Enhancers	Pancreas	Pancrea
19	chr17:37822800-37824800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr17:37823200-37824000	Enhancers	Spleen	Spleen
21	chr17:37823200-37824200	Bivalent Enhancer	Brain Hippocampus Middle	brain
22	chr17:37823200-37824200	Bivalent Enhancer	Colonic Mucosa	Colon
23	chr17:37823200-37824200	Bivalent Enhancer	Stomach Mucosa	stomach
24	chr17:37823200-37824400	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr17:37823200-37825200	Bivalent Enhancer	Rectal Mucosa Donor 31	rectum
26	chr17:37823400-37824000	Enhancers	Primary hematopoietic stem cells	blood
27	chr17:37823400-37824000	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
28	chr17:37823400-37824000	Flanking Bivalent TSS/Enh	HepG2	liver
29	chr17:37823400-37824200	Flanking Bivalent TSS/Enh	Fetal Intestine Large	intestine
30	chr17:37823400-37824400	Bivalent Enhancer	Adipose Nuclei	Adipose
31	chr17:37823400-37824800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
32	chr17:37823400-37825000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
33	chr17:37823400-37825200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr17:37823600-37824000	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
35	chr17:37823600-37824000	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
36	chr17:37823600-37824000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr17:37823600-37824000	Bivalent Enhancer	Fetal Brain Male	brain
38	chr17:37823600-37824200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
39	chr17:37823600-37824200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
40	chr17:37823600-37824200	Flanking Active TSS	Placenta Amnion	Placenta Amnion
41	chr17:37823600-37824400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
42	chr17:37823600-37824400	Active TSS	Right Atrium	heart
43	chr17:37823600-37824600	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
44	chr17:37823600-37824800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
45	chr17:37823600-37824800	Active TSS	Right Ventricle	heart
46	chr17:37823600-37825000	Active TSS	H9 Cell Line	embryonic stem cell
47	chr17:37823600-37825000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
48	chr17:37823600-37825000	Flanking Active TSS	Primary B cells from cord blood	blood
49	chr17:37823600-37825000	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
50	chr17:37823600-37825000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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