Variant report

Variant	rs7258891
Chromosome Location	chr19:18525701-18525702
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	ZNF143	chr19:18525488-18526754	K562	blood:	n/a	n/a
2	NFATC1	chr19:18525384-18525916	GM12878	blood:	n/a	n/a
3	HDAC2	chr19:18525505-18525812	HepG2	liver:	n/a	n/a
4	POLR2A	chr19:18525610-18530298	SK-N-MC	brain:	n/a	n/a
5	MAX	chr19:18525247-18525834	A549	lung:	n/a	chr19:18525511-18525520
6	POLR2A	chr19:18525342-18526889	U87	brain:	n/a	n/a
7	MAX	chr19:18525521-18525950	GM12878	blood:	n/a	chr19:18525876-18525886
8	POU2F2	chr19:18525278-18525720	GM12891	blood:	n/a	n/a
9	POLR2A	chr19:18525634-18526633	HL-60	blood:	n/a	n/a
10	SP1	chr19:18525213-18525725	GM12878	blood:	n/a	chr19:18525417-18525429 chr19:18525418-18525428 chr19:18525419-18525428 chr19:18525414-18525428 chr19:18525417-18525429
11	HEY1	chr19:18525294-18526716	K562	blood:	n/a	n/a
12	POLR2A	chr19:18525339-18526778	K562	blood:	n/a	n/a
13	EP300	chr19:18525361-18526758	K562	blood:	n/a	n/a
14	YY1	chr19:18525267-18525712	K562	blood:	n/a	n/a
15	POLR2A	chr19:18525272-18525885	HCT-116	colon:	n/a	n/a
16	MAX	chr19:18525204-18526862	K562	blood:	n/a	chr19:18525511-18525520 chr19:18525876-18525886 chr19:18526774-18526784
17	TBP	chr19:18525306-18525740	K562	blood:	n/a	n/a
18	POLR2A	chr19:18525418-18525856	HUVEC	blood vessel:	n/a	n/a
19	POLR2A	chr19:18525274-18526915	HUVEC	blood vessel:	n/a	n/a
20	CBX3	chr19:18524993-18526657	K562	blood:	n/a	n/a
21	POLR2A	chr19:18525346-18530410	K562	blood:	n/a	n/a
22	ELF1	chr19:18525290-18526671	K562	blood:	n/a	chr19:18526270-18526279
23	MYC	chr19:18525314-18526688	K562	blood:	n/a	chr19:18525511-18525520 chr19:18525876-18525886
24	E2F6	chr19:18525383-18526658	K562	blood:	n/a	chr19:18526075-18526085
25	MYC	chr19:18525158-18526673	K562	blood:	n/a	chr19:18525511-18525520 chr19:18525876-18525886
26	ZBTB7A	chr19:18525585-18526839	K562	blood:	n/a	chr19:18526073-18526082 chr19:18526105-18526113
27	TAF1	chr19:18525299-18525739	K562	blood:	n/a	n/a
28	MAX	chr19:18525531-18526668	NB4	blood:	n/a	chr19:18525876-18525886
29	POLR2A	chr19:18525403-18529035	HCT-116	colon:	n/a	n/a
30	SP1	chr19:18525201-18525706	A549	lung:	n/a	chr19:18525417-18525429 chr19:18525418-18525428 chr19:18525419-18525428 chr19:18525414-18525428 chr19:18525417-18525429
31	E2F6	chr19:18525333-18525720	K562	blood:	n/a	n/a
32	TBL1XR1	chr19:18525450-18525707	K562	blood:	n/a	n/a
33	POLR2A	chr19:18525194-18531443	K562	blood:	n/a	n/a
34	EBF1	chr19:18525371-18525733	GM12878	blood:	n/a	n/a
35	NR2F2	chr19:18524998-18529278	K562	blood:	n/a	n/a
36	NR2F2	chr19:18525200-18525859	K562	blood:	n/a	n/a
37	POLR2A	chr19:18525331-18526761	HL-60	blood:	n/a	n/a
38	PML	chr19:18525244-18525718	K562	blood:	n/a	n/a
39	MAZ	chr19:18525325-18526631	K562	blood:	n/a	chr19:18525511-18525520 chr19:18525876-18525886
40	POLR2A	chr19:18525344-18526755	K562	blood:	n/a	n/a
41	MAX	chr19:18525263-18525706	K562	blood:	n/a	chr19:18525511-18525520
42	EGR1	chr19:18525347-18526575	K562	blood:	n/a	chr19:18526045-18526054 chr19:18526269-18526280 chr19:18526352-18526365 chr19:18526040-18526050 chr19:18526038-18526052 chr19:18526036-18526050 chr19:18526040-18526051 chr19:18526034-18526056 chr19:18526039-18526052 chr19:18526040-18526051 chr19:18526040-18526050
43	POLR2A	chr19:18525271-18526725	K562	blood:	n/a	n/a
44	TCF12	chr19:18525416-18525915	A549	lung:	n/a	n/a
45	EP300	chr19:18525571-18525730	HepG2	liver:	n/a	n/a
46	MTA3	chr19:18525221-18526821	GM12878	blood:	n/a	n/a
47	POLR2A	chr19:18525251-18526731	K562	blood:	n/a	n/a
48	MXI1	chr19:18525647-18525918	K562	blood:	n/a	n/a
49	HEY1	chr19:18525244-18526783	K562	blood:	n/a	n/a
50	POLR2A	chr19:18525699-18526664	SK-N-MC	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:18385043..18394940-chr19:18518893..18533267,53	K562	blood:
2	chr19:18333703..18336599-chr19:18524425..18529905,5	K562	blood:
3	chr19:18520199..18523408-chr19:18523976..18531789,10	MCF-7	breast:
4	chr19:18495547..18503463-chr19:18525062..18531964,43	K562	blood:
5	chr19:18320883..18322593-chr19:18524287..18527226,2	K562	blood:
6	chr19:18450116..18452798-chr19:18524021..18525945,2	MCF-7	breast:
7	chr19:18399894..18406849-chr19:18524216..18528146,7	K562	blood:
8	chr19:18508054..18515743-chr19:18523957..18529414,9	K562	blood:
9	chr19:18448952..18453435-chr19:18523841..18530143,7	K562	blood:
10	chr19:18424650..18427071-chr19:18525382..18527314,2	K562	blood:
11	chr19:18388809..18393836-chr19:18524501..18532718,14	MCF-7	breast:
12	chr19:18340431..18343253-chr19:18523946..18525951,2	K562	blood:
13	chr19:18458615..18460578-chr19:18524334..18527055,2	MCF-7	breast:
14	chr19:18338900..18340811-chr19:18525374..18527248,2	K562	blood:
15	chr19:18383365..18408325-chr19:18518460..18533256,66	K562	blood:
16	chr19:18416874..18418645-chr19:18525016..18527028,2	K562	blood:
17	chr10:129924418..129925027-chr19:18525010..18525744,2	HCT-116	colon:
18	chr19:18422324..18424215-chr19:18524858..18526512,2	K562	blood:

Variant related genes	Relation type
SSBP4	TF binding region
ENSG00000130513	Chromatin interaction
ENSG00000130520	Chromatin interaction
ENSG00000130522	Chromatin interaction
ENSG00000175489	Chromatin interaction
ENSG00000148773	Chromatin interaction
ENSG00000105650	Chromatin interaction
ENSG00000267959	Chromatin interaction
ENSG00000221167	Chromatin interaction
ENSG00000130518	Chromatin interaction
ENSG00000241464	Chromatin interaction
ENSG00000130517	Chromatin interaction
ENSG00000264175	Chromatin interaction

Extended variants
information (count: 83 )
Associated
traits (count: 13 )

rSNPs within LD-proxies of this variant (count:72)

rs_ID	r²[population]
rs10402247	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10402322	0.81[ASN][1000 genomes]
rs10409346	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10409408	0.94[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10410797	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10416993	0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10418554	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10420384	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10423802	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10426768	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1045631	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11086110	0.88[CEU][hapmap];0.86[CHB][hapmap];0.85[CHD][hapmap];0.86[GIH][hapmap];0.85[TSI][hapmap];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11668704	0.85[ASN][1000 genomes]
rs11670392	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.84[GIH][hapmap];0.93[JPT][hapmap];0.80[MEX][hapmap];0.96[TSI][hapmap];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11672385	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.84[GIH][hapmap];0.93[JPT][hapmap];0.80[MEX][hapmap];0.96[TSI][hapmap];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11879757	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12980726	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12982295	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12983263	0.84[EUR][1000 genomes]
rs13344313	0.88[CHD][hapmap]
rs1469412	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.84[GIH][hapmap];0.93[JPT][hapmap];0.96[TSI][hapmap];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1469413	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1971093	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2013069	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2162797	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2303692	1.00[CEU][hapmap];0.88[CHB][hapmap];0.94[CHD][hapmap];0.84[GIH][hapmap];0.93[JPT][hapmap];0.84[MEX][hapmap];0.90[TSI][hapmap];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs28534973	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2891676	0.92[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs34213500	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];1.00[TSI][hapmap];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35004712	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs35336015	0.86[EUR][1000 genomes]
rs35742476	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.84[GIH][hapmap];0.93[JPT][hapmap];0.80[MEX][hapmap];0.93[TSI][hapmap];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4006662	0.81[EUR][1000 genomes]
rs4303657	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4580317	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4808135	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.93[JPT][hapmap];0.90[MEX][hapmap];0.93[TSI][hapmap];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4808802	0.88[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4808803	0.94[CEU][hapmap];0.88[CHB][hapmap];0.94[CHD][hapmap];0.84[GIH][hapmap];0.93[JPT][hapmap];0.96[TSI][hapmap];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4808805	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4808806	1.00[CHB][hapmap];0.92[JPT][hapmap];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4808807	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.81[GIH][hapmap];0.93[JPT][hapmap];0.90[MEX][hapmap];0.93[TSI][hapmap];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4808808	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4808811	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4808812	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs55715336	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs57923655	0.81[EUR][1000 genomes]
rs6512268	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6512269	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6512270	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6512271	0.82[ASN][1000 genomes]
rs7246788	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7247540	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7249760	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.84[GIH][hapmap];0.93[JPT][hapmap];0.90[MEX][hapmap];0.93[TSI][hapmap];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7251640	1.00[CHB][hapmap]
rs7252130	0.81[EUR][1000 genomes]
rs7252185	0.81[EUR][1000 genomes]
rs7255936	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7256530	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7259135	0.83[ASN][1000 genomes]
rs7507218	0.80[EUR][1000 genomes]
rs8100343	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8102717	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs8104247	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs8106068	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[CHD][hapmap];0.84[GIH][hapmap];0.93[JPT][hapmap];0.90[MEX][hapmap];0.93[TSI][hapmap];0.85[EUR][1000 genomes]
rs8106332	0.81[EUR][1000 genomes]
rs8111397	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs8111582	0.86[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs8111824	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];1.00[TSI][hapmap];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8112372	0.81[EUR][1000 genomes]
rs8112859	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs888668	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs888669	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.84[GIH][hapmap];0.93[JPT][hapmap];0.90[MEX][hapmap];0.96[TSI][hapmap];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	esv3323899	chr19:18343484-18620429	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	162 gene(s)	inside rSNPs	diseases
4	nsv911274	chr19:18440942-18691942	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
5	nsv1057795	chr19:18453362-18883844	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS 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	92 gene(s)	inside rSNPs	diseases
6	nsv543925	chr19:18453362-18883844	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
7	nsv428018	chr19:18454891-18663981	Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	61 gene(s)	inside rSNPs	diseases
8	nsv911275	chr19:18484922-18586759	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	50 gene(s)	inside rSNPs	diseases
9	nsv911276	chr19:18497141-18554972	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
10	nsv911277	chr19:18520231-18552139	Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
11	nsv1060687	chr19:18522527-18643218	Genic enhancers Strong transcription Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases

mRNA abundance (count:13)

SNP	Gene	Cis/trans	Tissue	Source
rs7258891	SSBP4	cis	cerebellum	SCAN
rs7258891	ZNF14	cis	parietal	SCAN
rs7258891	ISYNA1	cis	parietal	SCAN
rs7258891	SSBP4	Cis_1M	lymphoblastoid	RTeQTL
rs7258891	UBA52	cis	multi-tissue	Pritchard
rs7258891	UBA52	cis	brain	seeQTL
rs7258891	SSBP4	cis	lymphoblastoid	seeQTL
rs7258891	F2RL3	cis	cerebellum	SCAN
rs7258891	CHERP	cis	cerebellum	SCAN
rs7258891	SSBP4	cis	multi-tissue	Pritchard
rs7258891	LOC646044///SSBP4	Cis_1M	lymphoblastoid	RTeQTL
rs7258891	ABHD8	cis	parietal	SCAN
rs7258891	ELL	cis	multi-tissue	Pritchard

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18521600-18526400	Weak transcription	Pancreas	Pancrea
2	chr19:18521600-18527400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr19:18524200-18525800	Enhancers	Brain Germinal Matrix	brain
4	chr19:18524800-18526000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr19:18524800-18526000	Enhancers	Fetal Brain Male	brain
6	chr19:18524800-18526000	Enhancers	Fetal Thymus	thymus
7	chr19:18524800-18527200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr19:18524800-18527400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
9	chr19:18524800-18527600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr19:18524800-18527800	Flanking Active TSS	K562	blood
11	chr19:18524800-18528000	Enhancers	Primary hematopoietic stem cells	blood
12	chr19:18525000-18525800	Enhancers	Fetal Intestine Large	intestine
13	chr19:18525000-18525800	Enhancers	Fetal Intestine Small	intestine
14	chr19:18525000-18525800	Flanking Active TSS	Fetal Lung	lung
15	chr19:18525000-18525800	Enhancers	Ovary	ovary
16	chr19:18525000-18526000	Enhancers	Placenta	Placenta
17	chr19:18525000-18526200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
18	chr19:18525000-18526200	Enhancers	GM12878-XiMat	blood
19	chr19:18525000-18527200	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr19:18525000-18527200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr19:18525000-18527400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr19:18525000-18527400	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
23	chr19:18525000-18527400	Enhancers	Stomach Mucosa	stomach
24	chr19:18525000-18527600	Enhancers	Primary T helper naive cells from peripheral blood	blood
25	chr19:18525000-18527800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
26	chr19:18525000-18528000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
27	chr19:18525000-18528000	Enhancers	Primary T killer memory cells from peripheral blood	blood
28	chr19:18525000-18529600	Enhancers	Liver	Liver
29	chr19:18525000-18529600	Enhancers	Spleen	Spleen
30	chr19:18525200-18525800	Flanking Active TSS	Fetal Kidney	kidney
31	chr19:18525200-18525800	Enhancers	HUVEC	blood vessel
32	chr19:18525200-18526000	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr19:18525200-18526000	Enhancers	Duodenum Smooth Muscle	Duodenum
34	chr19:18525200-18526000	Enhancers	Rectal Mucosa Donor 31	rectum
35	chr19:18525200-18526000	Enhancers	Right Ventricle	heart
36	chr19:18525200-18526000	Enhancers	NHDF-Ad	bronchial
37	chr19:18525200-18526200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
38	chr19:18525200-18526200	Enhancers	Colon Smooth Muscle	Colon
39	chr19:18525200-18526400	Enhancers	Primary neutrophils fromperipheralblood	blood
40	chr19:18525200-18526400	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
41	chr19:18525200-18526800	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr19:18525200-18526800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
43	chr19:18525200-18526800	Flanking Active TSS	Osteobl	bone
44	chr19:18525200-18527200	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr19:18525200-18527400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr19:18525200-18527400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr19:18525200-18527400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
48	chr19:18525200-18527400	Enhancers	HMEC	breast
49	chr19:18525200-18527400	Enhancers	NH-A	brain
50	chr19:18525200-18528000	Enhancers	Brain Angular Gyrus	brain

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