Variant report

Variant	rs73292234
Chromosome Location	chr17:17584429-17584430
allele	A/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	MAFK	chr17:17584318-17584602	Hela-S3	cervix:	n/a	n/a
2	CTCF	chr17:17584371-17584813	H1-hESC	embryonic stem cell:	n/a	chr17:17584601-17584614 chr17:17584600-17584621 chr17:17584601-17584610 chr17:17584598-17584616 chr17:17584599-17584615
3	MAX	chr17:17584427-17584832	GM12878	blood:	n/a	chr17:17584460-17584470 chr17:17584569-17584579
4	CTCF	chr17:17584420-17584570	HRE	kidney:	n/a	n/a
5	YY1	chr17:17584362-17585269	HepG2	liver:	n/a	chr17:17584928-17584942 chr17:17584965-17584979 chr17:17584970-17584979
6	MXI1	chr17:17584358-17584934	HepG2	liver:	n/a	n/a
7	ZBTB7A	chr17:17584254-17586993	ECC-1	luminal epithelium:	n/a	chr17:17585395-17585404 chr17:17584964-17584973 chr17:17585784-17585792
8	TFAP2C	chr17:17584423-17586451	Hela-S3	cervix:	n/a	chr17:17585148-17585163
9	YY1	chr17:17584348-17584903	K562	blood:	n/a	n/a
10	MAX	chr17:17584171-17586520	HepG2	liver:	n/a	chr17:17584460-17584470 chr17:17584569-17584579 chr17:17584960-17584970
11	ZEB1	chr17:17584334-17584688	GM12878	blood:	n/a	chr17:17584437-17584444 chr17:17584434-17584446
12	PAX5	chr17:17584398-17586425	GM12892	blood:	n/a	chr17:17585556-17585565 chr17:17585224-17585233 chr17:17584950-17584959 chr17:17585549-17585566 chr17:17585222-17585231
13	SMC3	chr17:17584350-17584828	GM12878	blood:	n/a	chr17:17584566-17584576 chr17:17584600-17584614
14	ZBTB7A	chr17:17584365-17584641	HepG2	liver:	n/a	n/a
15	RAD21	chr17:17584222-17584959	ECC-1	luminal epithelium:	n/a	chr17:17584599-17584618
16	REST	chr17:17584150-17587378	H1-neurons	neurons:	n/a	chr17:17586117-17586130 chr17:17585274-17585287 chr17:17585661-17585674 chr17:17584557-17584570 chr17:17584457-17584470 chr17:17586267-17586277
17	TEAD4	chr17:17584355-17584998	ECC-1	luminal epithelium:	n/a	n/a
18	CTCF	chr17:17584360-17584910	K562	blood:	n/a	chr17:17584601-17584614 chr17:17584600-17584621 chr17:17584601-17584610 chr17:17584598-17584616 chr17:17584599-17584615
19	ZNF143	chr17:17584407-17585396	GM12878	blood:	n/a	chr17:17584569-17584579
20	CTCF	chr17:17584300-17584450	HEEpiC	esophagus:	n/a	n/a
21	BCLAF1	chr17:17584367-17584924	GM12878	blood:	n/a	chr17:17584561-17584574 chr17:17584549-17584562 chr17:17584565-17584578 chr17:17584603-17584616
22	RUNX3	chr17:17584331-17584707	GM12878	blood:	n/a	n/a
23	TCF12	chr17:17584002-17584963	A549	lung:	n/a	n/a
24	POLR2A	chr17:17584205-17587046	H1-neurons	neurons:	n/a	n/a
25	CEBPD	chr17:17584391-17584946	HepG2	liver:	n/a	n/a
26	CTCF	chr17:17584390-17584818	IMR90	lung:	n/a	chr17:17584601-17584614 chr17:17584600-17584621 chr17:17584601-17584610 chr17:17584598-17584616 chr17:17584599-17584615
27	ELF1	chr17:17584423-17585053	GM12878	blood:	n/a	n/a
28	SMC3	chr17:17584044-17587289	SK-N-SH	brain:	n/a	chr17:17586706-17586716 chr17:17584566-17584576 chr17:17584600-17584614 chr17:17586108-17586118
29	RUNX3	chr17:17584305-17584782	GM12878	blood:	n/a	n/a
30	TBL1XR1	chr17:17584363-17585042	GM12878	blood:	n/a	n/a
31	POLR2A	chr17:17584428-17586491	A549	lung:	n/a	n/a
32	MAZ	chr17:17584418-17584963	HepG2	liver:	n/a	chr17:17584460-17584470 chr17:17584569-17584579
33	CHD1	chr17:17584053-17587549	IMR90	lung:	n/a	chr17:17585399-17585409 chr17:17584955-17584965
34	MAX	chr17:17584394-17585007	A549	lung:	n/a	chr17:17584460-17584470 chr17:17584569-17584579 chr17:17584960-17584970
35	RAD21	chr17:17584320-17586985	IMR90	lung:	n/a	chr17:17584599-17584618 chr17:17586614-17586627 chr17:17585966-17585979
36	ZNF263	chr17:17583857-17585038	HEK293-T-REx	kidney:	n/a	chr17:17584983-17584992
37	CTCF	chr17:17584420-17584570	GM12878	blood:	n/a	n/a
38	CTCF	chr17:17584300-17584450	HPAF	blood vessel:	n/a	n/a
39	TCF3	chr17:17584338-17585110	GM12878	blood:	n/a	n/a
40	RAD21	chr17:17584388-17584793	HepG2	liver:	n/a	chr17:17584599-17584618
41	CTCF	chr17:17583878-17586930	A549	lung:	n/a	chr17:17585965-17585978 chr17:17586704-17586713 chr17:17584601-17584614 chr17:17584600-17584621 chr17:17584601-17584610 chr17:17584959-17584972 chr17:17584598-17584616 chr17:17584599-17584615 chr17:17586744-17586757
42	ZBTB7A	chr17:17584227-17586957	ECC-1	luminal epithelium:	n/a	chr17:17585395-17585404 chr17:17584964-17584973 chr17:17585784-17585792
43	RAD21	chr17:17584366-17584935	MCF-7	breast:	n/a	chr17:17584599-17584618
44	CTCF	chr17:17584361-17584727	K562	blood:	n/a	chr17:17584601-17584614 chr17:17584600-17584621 chr17:17584601-17584610 chr17:17584598-17584616 chr17:17584599-17584615
45	RAD21	chr17:17584340-17584841	H1-hESC	embryonic stem cell:	n/a	chr17:17584599-17584618
46	GABPA	chr17:17584385-17585008	H1-hESC	embryonic stem cell:	n/a	chr17:17584933-17584942 chr17:17584569-17584578
47	CTCF	chr17:17584428-17584724	SK-N-SH_RA	brain:	n/a	chr17:17584601-17584614 chr17:17584600-17584621 chr17:17584601-17584610 chr17:17584598-17584616 chr17:17584599-17584615
48	CTCF	chr17:17584422-17584748	Spleen_OC	spleen:	n/a	chr17:17584601-17584614 chr17:17584600-17584621 chr17:17584601-17584610 chr17:17584598-17584616 chr17:17584599-17584615
49	CTCF	chr17:17584280-17584430	MCF-7	breast:	n/a	n/a
50	MXI1	chr17:17584320-17587355	IMR90	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:17584403-17584453	GM06990	blood:	n/a
2	chr17:17584403-17584453	SK-N-SH_RA	brain:	n/a
3	chr17:17584403-17584453	HCT-116	colon:	n/a
4	chr17:17584403-17584453	HAEpiC	amniotic membrane:	n/a
5	chr17:17584403-17584453	SAEC	small airway:	n/a
6	chr17:17584403-17584453	RPTEC	kidney:	n/a
7	chr17:17584403-17584453	T-47D	breast:	n/a
8	chr17:17584403-17584453	A549	lung:	n/a
9	chr17:17584403-17584453	HUVEC	blood vessel:	n/a
10	chr17:17584403-17584453	H1-hESC	embryonic stem cell:	embryo
11	chr17:17584403-17584453	AG09309	skin:	n/a
12	chr17:17584403-17584453	IMR90	lung:	fetal
13	chr17:17584403-17584453	PFSK-1	brain:	n/a
14	chr17:17584403-17584453	Hepatocyte	liver:	n/a
15	chr17:17584403-17584453	AG10803	skin:	n/a
16	chr17:17584403-17584453	PrEC	prostate:	n/a
17	chr17:17584403-17584453	K562	blood:	n/a
18	chr17:17584403-17584453	AG09319	gingival:	n/a
19	chr17:17584403-17584453	NHDF-neo	bronchial:	n/a
20	chr17:17584403-17584453	SK-N-MC	brain:	n/a
21	chr17:17584403-17584453	U87	brain:	n/a
22	chr17:17584403-17584453	ProgFib	skin:	n/a
23	chr17:17584403-17584453	HIPEpiC	eye:	n/a
24	chr17:17584403-17584453	Jurkat	blood:	n/a
25	chr17:17584403-17584453	AG04450	lung:	fetal
26	chr17:17584403-17584453	HCM	heart:	n/a
27	chr17:17584403-17584453	CMK	blood:	n/a
28	chr17:17584403-17584453	GM12891	blood:	n/a
29	chr17:17584403-17584453	BJ	skin:	n/a
30	chr17:17584403-17584453	NB4	blood:	n/a
31	chr17:17584403-17584453	HepG2	liver:	n/a
32	chr17:17584403-17584453	AoSMC	blood vessel:	n/a
33	chr17:17584403-17584453	MCF-7	breast:	n/a
34	chr17:17584403-17584453	HRCEpiC	kidney:	n/a
35	chr17:17584403-17584453	MCF10A-Er-Src	breast:	n/a
36	chr17:17584403-17584453	HEK293	kidney:	embryo
37	chr17:17584403-17584453	BE2_C	brain:	n/a
38	chr17:17584403-17584453	HPAEpiC	pulmonary alveolar:	n/a
39	chr17:17584403-17584453	SK-N-SH	brain:	n/a
40	chr17:17584403-17584453	AG04449	skin:	fetal
41	chr17:17584403-17584453	LNCaP	prostate:	n/a
42	chr17:17584403-17584453	HRE	kidney:	n/a
43	chr17:17584403-17584453	GM19239	blood:	n/a
44	chr17:17584403-17584453	HMEC	breast:	n/a
45	chr17:17584403-17584453	HNPCEpiC	eye:	n/a
46	chr17:17584403-17584453	NT2-D1	testis:	n/a
47	chr17:17584403-17584453	HEEpiC	esophagus:	n/a
48	chr17:17584403-17584453	PANC-1	pancreas:	n/a
49	chr17:17584403-17584453	Hela-S3	cervix:	n/a
50	chr17:17584403-17584453	ECC-1	luminal epithelium:	n/a

No.	Distal block	Cell Line	Cell type
1	chr17:17582120..17584481-chr17:17669635..17672296,2	K562	blood:
2	chr17:17583267..17586800-chr17:17714001..17718221,4	K562	blood:
3	chr17:17584110..17584675-chr17:17763112..17763841,2	MCF-7	breast:
4	chr17:17581707..17587972-chr17:17684185..17691006,14	MCF-7	breast:
5	chr17:17584083..17584649-chr17:17715246..17716136,2	MCF-7	breast:
6	chr17:17584228..17586367-chr17:17721759..17723604,3	MCF-7	breast:
7	chr17:17583605..17586318-chr17:17753777..17755939,2	K562	blood:
8	chr17:17584192..17584734-chr17:17642875..17643692,2	MCF-7	breast:
9	chr17:17583924..17586191-chr17:17941715..17944094,3	K562	blood:
10	chr17:17583519..17585283-chr17:17719170..17722055,2	MCF-7	breast:
11	chr17:17583640..17587401-chr17:17713270..17717474,6	MCF-7	breast:
12	chr17:17584408..17586554-chr17:17725797..17727625,2	K562	blood:
13	chr17:17582541..17589441-chr17:17738170..17742091,10	K562	blood:
14	chr17:17583171..17587600-chr17:17683205..17687633,5	MCF-7	breast:
15	chr17:17583267..17584889-chr17:17715443..17717177,2	K562	blood:
16	chr17:17580850..17587926-chr17:17737733..17744809,17	MCF-7	breast:
17	chr17:17584137..17584962-chr17:17739599..17740212,2	HCT-116	colon:
18	chr17:17582010..17584605-chr17:17704588..17707472,2	K562	blood:
19	chr17:17583537..17586679-chr17:17711908..17715201,3	MCF-7	breast:
20	chr17:17583643..17586896-chr17:17724231..17729521,8	MCF-7	breast:

Variant related genes	Relation type
SMCR2	TF binding region
RAI1	TF binding region
RAI1	CpG island
SMCR2	CpG island
ENSG00000108557	Chromatin interaction
ENSG00000171953	Chromatin interaction
ENSG00000207839	Chromatin interaction
ENSG00000072310	Chromatin interaction
ENSG00000141034	Chromatin interaction
ENSG00000175662	Chromatin interaction

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs73292253	0.90[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv907748	chr17:17412032-17782404	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
2	nsv1065270	chr17:17430116-17823086	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription Active TSS 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 miRNA target site	91 gene(s)	inside rSNPs	diseases
3	nsv543236	chr17:17430116-17823086	Bivalent Enhancer Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers 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 miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
4	nsv833384	chr17:17491483-17645648	Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
5	nsv869118	chr17:17509896-17599850	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
6	nsv907752	chr17:17569012-17750907	Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
7	nsv531183	chr17:17571035-18205309	Genic enhancers Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer 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	123 gene(s)	inside rSNPs	diseases
8	nsv907753	chr17:17573539-17747289	Genic enhancers Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
9	nsv907754	chr17:17573539-17782404	Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS 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	78 gene(s)	inside rSNPs	diseases
10	nsv1061126	chr17:17578826-17803194	Strong transcription Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
11	nsv543238	chr17:17578826-17803194	Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Bivalent Enhancer 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 miRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
12	nsv543239	chr17:17580295-17599851	Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
13	nsv907755	chr17:17581184-17610587	Enhancers Genic enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
14	esv3369275	chr17:17583127-17586825	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
15	esv3443065	chr17:17583652-17586200	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
16	nsv827910	chr17:17583901-17586576	Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
17	esv3413919	chr17:17583902-17586600	Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:17580600-17585200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
2	chr17:17580800-17584600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr17:17581000-17584800	Weak transcription	Primary T cells from cord blood	blood
4	chr17:17581000-17586400	Weak transcription	Fetal Heart	heart
5	chr17:17581400-17584800	Weak transcription	HUVEC	blood vessel
6	chr17:17582000-17584600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr17:17583600-17586800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
8	chr17:17583800-17584600	Enhancers	Fetal Thymus	thymus
9	chr17:17584000-17584600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr17:17584000-17584600	Enhancers	Primary B cells from peripheral blood	blood
11	chr17:17584000-17584600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
12	chr17:17584000-17584600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr17:17584000-17584600	Enhancers	Fetal Intestine Small	intestine
14	chr17:17584000-17584600	Flanking Bivalent TSS/Enh	HepG2	liver
15	chr17:17584000-17586000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr17:17584000-17586600	Active TSS	Hela-S3	cervix
17	chr17:17584200-17584600	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
18	chr17:17584200-17584600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr17:17584200-17584600	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr17:17584200-17584600	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr17:17584200-17584600	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr17:17584200-17584600	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
23	chr17:17584200-17584600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr17:17584200-17584600	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr17:17584200-17584600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr17:17584200-17584600	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr17:17584200-17584600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
28	chr17:17584200-17584600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
29	chr17:17584200-17584600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr17:17584200-17584600	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr17:17584200-17584600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr17:17584200-17584600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr17:17584200-17584600	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
34	chr17:17584200-17584600	Enhancers	Brain Substantia Nigra	brain
35	chr17:17584200-17584600	Enhancers	Esophagus	oesophagus
36	chr17:17584200-17584600	Enhancers	Fetal Brain Male	brain
37	chr17:17584200-17584600	Flanking Active TSS	Fetal Intestine Large	intestine
38	chr17:17584200-17584600	Enhancers	Fetal Lung	lung
39	chr17:17584200-17584600	Flanking Active TSS	Fetal Muscle Trunk	muscle
40	chr17:17584200-17584600	Flanking Active TSS	Fetal Muscle Leg	muscle
41	chr17:17584200-17584600	Enhancers	Fetal Stomach	stomach
42	chr17:17584200-17584600	Enhancers	Left Ventricle	heart
43	chr17:17584200-17584600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
44	chr17:17584200-17584600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
45	chr17:17584200-17584600	Flanking Active TSS	Stomach Smooth Muscle	stomach
46	chr17:17584200-17584600	Enhancers	Spleen	Spleen
47	chr17:17584200-17584600	Flanking Active TSS	A549	lung
48	chr17:17584200-17584600	Flanking Active TSS	Dnd41	blood
49	chr17:17584200-17584600	Flanking Active TSS	GM12878-XiMat	blood
50	chr17:17584200-17584600	Flanking Active TSS	HMEC	breast

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