Variant report

Variant	rs10417985
Chromosome Location	chr19:42377133-42377134
allele	C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:216)
CpG islands
(count:0)
Chromatin interactive
region (count:25)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:216 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr19:42375827-42378940	MCF10A-Er-Src	breast:	n/a	n/a
2	POLR2A	chr19:42376950-42377690	HepG2	liver:	n/a	n/a
3	ATF2	chr19:42376933-42377643	GM12878	blood:	n/a	n/a
4	RCOR1	chr19:42377070-42377584	Hela-S3	cervix:	n/a	n/a
5	POLR2A	chr19:42375185-42377803	GM12891	blood:	n/a	n/a
6	POLR2A	chr19:42375739-42377700	HepG2	liver:	n/a	n/a
7	JUND	chr19:42374323-42378847	A549	lung:	n/a	n/a
8	ELK1	chr19:42377126-42377563	K562	blood:	n/a	n/a
9	POLR2A	chr19:42375552-42378314	HUVEC	blood vessel:	n/a	n/a
10	POLR2A	chr19:42375554-42377714	GM12891	blood:	n/a	n/a
11	SIX5	chr19:42375075-42377986	A549	lung:	n/a	n/a
12	POU2F2	chr19:42377011-42377586	GM12878	blood:	n/a	n/a
13	PBX3	chr19:42375813-42377861	A549	lung:	n/a	chr19:42376117-42376126
14	POLR2A	chr19:42370162-42377852	GM12878	blood:	n/a	n/a
15	PBX3	chr19:42376942-42377739	SK-N-SH	brain:	n/a	n/a
16	POLR2A	chr19:42371518-42378813	U87	brain:	n/a	n/a
17	MAFK	chr19:42376991-42377539	Hela-S3	cervix:	n/a	n/a
18	POLR2A	chr19:42375167-42377755	K562	blood:	n/a	n/a
19	GATA3	chr19:42375754-42377876	A549	lung:	n/a	n/a
20	POLR2A	chr19:42375841-42377810	HEK293	kidney:	n/a	n/a
21	RAD21	chr19:42377118-42377630	H1-hESC	embryonic stem cell:	n/a	chr19:42377386-42377400
22	NFIC	chr19:42376910-42377331	ECC-1	luminal epithelium:	n/a	n/a
23	STAT5A	chr19:42375535-42377818	GM12878	blood:	n/a	chr19:42376131-42376138 chr19:42375697-42375709 chr19:42375697-42375705 chr19:42376317-42376325
24	POLR2A	chr19:42375445-42377854	HL-60	blood:	n/a	n/a
25	POLR2A	chr19:42375801-42378727	IMR90	lung:	n/a	n/a
26	RCOR1	chr19:42377046-42377568	K562	blood:	n/a	n/a
27	POLR2A	chr19:42370055-42377966	GM12892	blood:	n/a	n/a
28	NFATC1	chr19:42375542-42378161	GM12878	blood:	n/a	n/a
29	ETS1	chr19:42375621-42377862	A549	lung:	n/a	chr19:42375691-42375706 chr19:42375830-42375844 chr19:42377510-42377523 chr19:42376130-42376141 chr19:42375832-42375843 chr19:42377293-42377302 chr19:42375691-42375704 chr19:42376128-42376141 chr19:42376129-42376143
30	MAFF	chr19:42377026-42377529	K562	blood:	n/a	n/a
31	POLR2A	chr19:42376857-42377662	K562	blood:	n/a	n/a
32	EP300	chr19:42375705-42377895	A549	lung:	n/a	chr19:42377206-42377219 chr19:42375823-42375836
33	POLR2A	chr19:42375203-42377793	K562	blood:	n/a	n/a
34	NRF1	chr19:42377118-42377531	H1-hESC	embryonic stem cell:	n/a	n/a
35	RAD21	chr19:42377022-42377794	A549	lung:	n/a	chr19:42377386-42377400
36	SP1	chr19:42375761-42377795	A549	lung:	n/a	n/a
37	SIN3AK20	chr19:42377055-42377393	H1-hESC	embryonic stem cell:	n/a	n/a
38	TEAD4	chr19:42377032-42377538	K562	blood:	n/a	n/a
39	POLR2A	chr19:42375476-42377879	A549	lung:	n/a	n/a
40	CREB1	chr19:42375888-42377693	A549	lung:	n/a	n/a
41	CHD2	chr19:42376988-42377639	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr19:42375737-42377627	H1-hESC	embryonic stem cell:	n/a	n/a
43	SP1	chr19:42375715-42377892	A549	lung:	n/a	n/a
44	TEAD4	chr19:42377064-42377703	ECC-1	luminal epithelium:	n/a	n/a
45	TCF12	chr19:42375707-42377774	A549	lung:	n/a	chr19:42377548-42377555
46	GTF2F1	chr19:42377075-42377549	Hela-S3	cervix:	n/a	n/a
47	FOXA2	chr19:42376655-42377683	A549	lung:	n/a	n/a
48	POLR2A	chr19:42363421-42379264	HepG2	liver:	n/a	n/a
49	CTCF	chr19:42377091-42377709	K562	blood:	n/a	chr19:42377229-42377247 chr19:42377224-42377245 chr19:42377386-42377399
50	REST	chr19:42376141-42377775	A549	lung:	n/a	chr19:42376291-42376300

No data

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:42375695..42377388-chr19:42406535..42408788,2	K562	blood:
2	chr19:42367000..42368909-chr19:42375795..42378988,3	MCF-7	breast:
3	chr19:42375660..42379259-chr19:42380493..42384437,4	MCF-7	breast:
4	chr19:42370513..42373649-chr19:42375625..42377894,4	MCF-7	breast:
5	chr19:42376370..42377844-chr19:42455348..42456066,5	K562	blood:
6	chr19:42376980..42377675-chr19:42438677..42439657,3	MCF-7	breast:
7	chr19:42374454..42377744-chr19:42431362..42433284,5	K562	blood:
8	chr19:42368937..42370473-chr19:42375983..42377700,2	MCF-7	breast:
9	chr19:42373799..42381047-chr19:42460989..42465067,14	K562	blood:
10	chr19:42375921..42378052-chr19:42410713..42412528,2	MCF-7	breast:
11	chr19:42375717..42378779-chr19:42460823..42464081,5	MCF-7	breast:
12	chr19:42374516..42378766-chr19:42444244..42446935,5	K562	blood:
13	chr19:42354421..42356282-chr19:42374725..42377333,2	MCF-7	breast:
14	chr19:42376907..42377725-chr19:42462018..42462632,4	MCF-7	breast:
15	chr19:42375846..42378575-chr19:42437686..42441355,5	MCF-7	breast:
16	chr19:42374823..42377954-chr19:42385843..42389445,4	MCF-7	breast:
17	chr19:42373353..42379670-chr19:42459996..42464717,12	K562	blood:
18	chr19:42377082..42377816-chr19:42455455..42456477,4	MCF-7	breast:
19	chr19:42376866..42377852-chr19:42461645..42462448,2	K562	blood:
20	chr19:42375829..42377976-chr19:42413032..42416255,3	MCF-7	breast:
21	chr19:42375885..42381575-chr19:42432655..42439530,9	K562	blood:
22	chr19:42374905..42377918-chr19:42453712..42457623,5	K562	blood:
23	chr19:42374905..42378139-chr19:42452312..42458975,8	K562	blood:
24	chr19:42377016..42377922-chr19:42438274..42439260,2	K562	blood:
25	chr19:42374727..42377526-chr19:42531576..42534265,2	MCF-7	breast:

No data

Variant related genes	Relation type
CD79A	TF binding region
ENSG00000268041	Chromatin interaction
ENSG00000105404	Chromatin interaction
ENSG00000076928	Chromatin interaction
ENSG00000105369	Chromatin interaction

Extended variants
information (count: 63 )
Associated
traits (count: 8 )

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10404939	1.00[CHB][hapmap];0.85[CHD][hapmap];0.86[GIH][hapmap];0.83[JPT][hapmap]
rs10405900	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10408367	0.91[CHB][hapmap];0.83[JPT][hapmap];0.87[LWK][hapmap];0.84[MKK][hapmap]
rs10414356	0.81[ASN][1000 genomes]
rs10414823	0.95[CHB][hapmap]
rs10415452	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10416824	0.91[CHB][hapmap];0.83[JPT][hapmap]
rs10500284	1.00[CHB][hapmap];0.90[CHD][hapmap];0.87[JPT][hapmap];0.83[ASN][1000 genomes]
rs12461099	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12461131	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12976571	1.00[CHB][hapmap];0.83[JPT][hapmap]
rs12979253	0.95[CHB][hapmap];0.83[CHD][hapmap]
rs12984383	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1366610	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1428922	0.85[CEU][hapmap];0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1457144	1.00[CHB][hapmap];0.83[CHD][hapmap];0.88[GIH][hapmap];0.83[JPT][hapmap]
rs1870092	1.00[CHB][hapmap];0.85[CHD][hapmap];0.83[JPT][hapmap];0.80[LWK][hapmap]
rs2008798	0.90[CHB][hapmap];0.83[JPT][hapmap]
rs2075749	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2075750	0.92[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.98[TSI][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2075752	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];0.82[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2075754	0.96[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2199829	0.91[CHB][hapmap];0.83[JPT][hapmap];0.91[LWK][hapmap];1.00[YRI][hapmap]
rs2290695	0.81[ASW][hapmap];1.00[CHB][hapmap];0.85[CHD][hapmap];0.86[GIH][hapmap];0.81[LWK][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs2305809	0.90[ASW][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap];0.86[GIH][hapmap];0.86[JPT][hapmap];0.91[LWK][hapmap];0.82[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs3786536	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3786538	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3810153	0.89[CEU][hapmap];0.95[CHB][hapmap];0.87[GIH][hapmap];0.91[JPT][hapmap];0.80[MKK][hapmap];0.82[TSI][hapmap];0.81[AMR][1000 genomes];0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3922888	1.00[CHB][hapmap];0.85[CHD][hapmap];0.86[GIH][hapmap];0.87[JPT][hapmap];0.81[ASN][1000 genomes]
rs4130852	0.81[ASN][1000 genomes]
rs4803511	1.00[CHB][hapmap];0.85[CHD][hapmap];0.86[GIH][hapmap];0.87[JPT][hapmap];0.81[ASN][1000 genomes]
rs4803512	0.95[CHB][hapmap];0.85[CHD][hapmap];0.86[GIH][hapmap];0.87[JPT][hapmap];0.81[ASN][1000 genomes]
rs58857981	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6509001	0.83[ASN][1000 genomes]
rs6509002	0.90[ASW][hapmap];0.91[CHB][hapmap];0.83[CHD][hapmap];0.86[GIH][hapmap];0.87[JPT][hapmap]
rs7250787	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7251336	0.82[CHB][hapmap];0.91[LWK][hapmap];1.00[YRI][hapmap]
rs7251960	0.82[CHB][hapmap]
rs7254214	0.90[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.91[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7257666	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7258163	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7259596	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7259967	0.85[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs734107	0.91[CHB][hapmap];0.83[JPT][hapmap]
rs73549152	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs8102670	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs8104958	1.00[CHB][hapmap];0.85[CHD][hapmap];0.86[GIH][hapmap];0.83[JPT][hapmap]
rs8106505	0.95[CHB][hapmap]
rs8113283	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs8113641	0.89[CHB][hapmap];0.83[JPT][hapmap]
rs873282	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs882520	0.89[CEU][hapmap];0.95[CHB][hapmap];0.91[JPT][hapmap];0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs891167	0.85[CEU][hapmap];0.83[CHB][hapmap];0.87[GIH][hapmap];0.91[JPT][hapmap];0.83[MEX][hapmap];0.85[MKK][hapmap];0.85[TSI][hapmap];0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs899662	0.86[CHB][hapmap];0.83[JPT][hapmap];0.87[LWK][hapmap]
rs930102	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv522854	chr19:42120283-42931004	Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
2	nsv1061878	chr19:42325490-42416056	Strong transcription Flanking Active TSS Weak transcription Genic enhancers Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv911776	chr19:42343526-42416056	Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
4	nsv911777	chr19:42357455-42521108	Bivalent/Poised TSS Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
5	nsv520239	chr19:42357455-42931004	Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats 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	nsv911778	chr19:42358362-42416056	Strong transcription Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
7	esv1805469	chr19:42367635-42798851	Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Weak transcription 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
8	nsv932623	chr19:42370540-42378620	Genic enhancers Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region miRNA	9 gene(s)	inside rSNPs	diseases

mRNA abundance (count:8)

SNP	Gene	Cis/trans	Tissue	Source
rs10417985	LIG1	cis	parietal	SCAN
rs10417985	IGFL1	cis	parietal	SCAN
rs10417985	RABAC1	Cis_1M	lymphoblastoid	RTeQTL
rs10417985	PPP5C	cis	parietal	SCAN
rs10417985	SLC1A5	cis	parietal	SCAN
rs10417985	ZNF575	cis	parietal	SCAN
rs10417985	EXOC3L2	cis	cerebellum	SCAN
rs10417985	GLTSCR2	cis	cerebellum	SCAN

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:42366400-42377600	Strong transcription	Fetal Brain Female	brain
2	chr19:42367200-42377200	Strong transcription	Brain Inferior Temporal Lobe	brain
3	chr19:42367600-42379200	Weak transcription	Fetal Brain Male	brain
4	chr19:42368800-42377400	Strong transcription	Brain Germinal Matrix	brain
5	chr19:42369200-42377200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr19:42369400-42377600	Genic enhancers	Fetal Thymus	thymus
7	chr19:42369600-42377400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr19:42369600-42386400	Weak transcription	Fetal Kidney	kidney
9	chr19:42370400-42377600	Strong transcription	Cortex derived primary cultured neurospheres	brain
10	chr19:42372200-42377200	Strong transcription	Brain Angular Gyrus	brain
11	chr19:42372200-42377400	Strong transcription	Stomach Smooth Muscle	stomach
12	chr19:42372600-42377600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
13	chr19:42372600-42377800	Genic enhancers	Spleen	Spleen
14	chr19:42373800-42381400	Enhancers	Primary hematopoietic stem cells	blood
15	chr19:42374000-42378200	Weak transcription	Ovary	ovary
16	chr19:42374400-42377200	Genic enhancers	Thymus	Thymus
17	chr19:42374600-42377600	Strong transcription	Osteobl	bone
18	chr19:42374600-42379800	Enhancers	Primary T helper naive cells from peripheral blood	blood
19	chr19:42374600-42386600	Weak transcription	Right Atrium	heart
20	chr19:42374800-42377200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr19:42374800-42377400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
22	chr19:42374800-42378400	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr19:42374800-42379600	Weak transcription	K562	blood
24	chr19:42374800-42380600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
25	chr19:42374800-42381400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr19:42374800-42381400	Enhancers	Primary T cells fromperipheralblood	blood
27	chr19:42374800-42381400	Weak transcription	Rectal Smooth Muscle	rectum
28	chr19:42374800-42381400	Weak transcription	Small Intestine	intestine
29	chr19:42374800-42381800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr19:42375000-42377200	Strong transcription	Fetal Intestine Small	intestine
31	chr19:42375000-42377400	Genic enhancers	Fetal Muscle Leg	muscle
32	chr19:42375000-42381200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
33	chr19:42375200-42377200	Genic enhancers	Placenta	Placenta
34	chr19:42375400-42380200	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr19:42375400-42386200	Weak transcription	Hela-S3	cervix
36	chr19:42376000-42381000	Weak transcription	HepG2	liver
37	chr19:42376000-42386400	Weak transcription	Brain Anterior Caudate	brain
38	chr19:42376000-42386400	Weak transcription	Fetal Lung	lung
39	chr19:42376000-42386600	Weak transcription	HSMMtube	muscle
40	chr19:42376200-42377400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr19:42376200-42377400	Genic enhancers	Pancreas	Pancrea
42	chr19:42376200-42377600	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr19:42376200-42377600	Weak transcription	HUES64 Cell Line	embryonic stem cell
44	chr19:42376200-42377800	Enhancers	Rectal Mucosa Donor 29	rectum
45	chr19:42376200-42378800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr19:42376200-42379000	Weak transcription	Aorta	Aorta
47	chr19:42376200-42379400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr19:42376200-42379400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr19:42376200-42379400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
50	chr19:42376200-42380200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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