Variant report

Variant	rs17164382
Chromosome Location	chr4:1161190-1161191
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:308)
CpG islands
(count:61)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:308 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	TBL1XR1	chr4:1160929-1161620	K562	blood:	n/a	n/a
2	MAZ	chr4:1160568-1162014	IMR90	lung:	n/a	chr4:1160594-1160605 chr4:1160595-1160604 chr4:1161615-1161624 chr4:1160594-1160605
3	SIN3AK20	chr4:1159401-1161758	PFSK-1	brain:	n/a	n/a
4	CTCF	chr4:1160967-1161239	MCF-7	breast:	n/a	n/a
5	RAD21	chr4:1160741-1161766	HCT-116	colon:	n/a	n/a
6	CTCF	chr4:1160925-1161249	Lung_OC	lung:	n/a	n/a
7	RAD21	chr4:1160940-1161270	Hela-S3	cervix:	n/a	n/a
8	MAX	chr4:1160993-1161691	H1-hESC	embryonic stem cell:	n/a	chr4:1161615-1161624
9	ELK1	chr4:1161057-1161443	K562	blood:	n/a	n/a
10	STAT5A	chr4:1160660-1161581	GM12878	blood:	n/a	n/a
11	CTCF	chr4:1160919-1161197	A549	lung:	n/a	n/a
12	CTCF	chr4:1160633-1161789	SK-N-SH	brain:	n/a	chr4:1161755-1161768
13	POLR2A	chr4:1160957-1161488	IMR90	lung:	n/a	n/a
14	CTCF	chr4:1160931-1161225	GM10248	blood:	n/a	n/a
15	POLR2A	chr4:1160975-1161779	NB4	blood:	n/a	n/a
16	YY1	chr4:1160961-1161233	K562	blood:	n/a	n/a
17	POLR2A	chr4:1160847-1161941	K562	blood:	n/a	n/a
18	YY1	chr4:1160955-1161244	HCT-116	colon:	n/a	n/a
19	CCNT2	chr4:1161037-1161479	K562	blood:	n/a	n/a
20	CTCF	chr4:1160919-1161311	A549	lung:	n/a	n/a
21	YY1	chr4:1160933-1161296	GM12892	blood:	n/a	n/a
22	CTCF	chr4:1160988-1161197	HepG2	liver:	n/a	n/a
23	GABPA	chr4:1160944-1161589	H1-hESC	embryonic stem cell:	n/a	n/a
24	IRF1	chr4:1161027-1161744	K562	blood:	n/a	chr4:1161540-1161554
25	TCF3	chr4:1160928-1161402	GM12878	blood:	n/a	n/a
26	CTCF	chr4:1161040-1161190	HFF	foreskin:	n/a	n/a
27	CTCF	chr4:1161040-1161190	GM06990	blood:	n/a	n/a
28	TBP	chr4:1160893-1161698	K562	blood:	n/a	n/a
29	SMC3	chr4:1160859-1161867	GM12878	blood:	n/a	n/a
30	POLR2A	chr4:1161005-1161782	GM12892	blood:	n/a	n/a
31	CTCF	chr4:1160961-1161235	ProgFib	skin:	n/a	n/a
32	RAD21	chr4:1160932-1161299	SK-N-SH_RA	brain:	n/a	n/a
33	RCOR1	chr4:1160891-1161762	K562	blood:	n/a	n/a
34	CTCF	chr4:1160953-1161254	GM10266	blood:	n/a	n/a
35	CTCF	chr4:1160948-1161245	GM19239	blood:	n/a	n/a
36	CREB1	chr4:1160911-1161771	H1-hESC	embryonic stem cell:	n/a	n/a
37	RAD21	chr4:1160897-1161282	HepG2	liver:	n/a	n/a
38	ZMIZ1	chr4:1160994-1161612	K562	blood:	n/a	n/a
39	RAD21	chr4:1160913-1161373	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr4:1161040-1161190	HA-sp	spinal cord:	n/a	n/a
41	POLR2A	chr4:1161033-1161953	H1-hESC	embryonic stem cell:	n/a	n/a
42	TCF7L2	chr4:1161011-1161711	HCT-116	colon:	n/a	n/a
43	EP300	chr4:1160969-1161860	GM12878	blood:	n/a	n/a
44	CTCF	chr4:1160977-1161212	Hela-S3	cervix:	n/a	n/a
45	POLR2A	chr4:1160972-1161729	GM18526	blood:	n/a	n/a
46	CTCF	chr4:1160813-1161386	MCF-7	breast:	n/a	n/a
47	GTF2F1	chr4:1161099-1161527	K562	blood:	n/a	n/a
48	CTCF	chr4:1160978-1161230	A549	lung:	n/a	n/a
49	CTCF	chr4:1160966-1161266	T-47D	breast:	n/a	n/a
50	PML	chr4:1160735-1161842	GM12878	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:1161157-1161207	HCM	heart:	n/a
2	chr4:1161157-1161207	HRPEpiC	eye:	n/a
3	chr4:1161157-1161207	HIPEpiC	eye:	n/a
4	chr4:1161157-1161207	HPAEpiC	pulmonary alveolar:	n/a
5	chr4:1161157-1161207	U87	brain:	n/a
6	chr4:1161157-1161207	NHBE	bronchial:	n/a
7	chr4:1161157-1161207	SKMC	muscle:	n/a
8	chr4:1161157-1161207	MCF10A-Er-Src	breast:	n/a
9	chr4:1161157-1161207	HCT-116	colon:	n/a
10	chr4:1161157-1161207	SK-N-SH_RA	brain:	n/a
11	chr4:1161157-1161207	HCF	heart:	n/a
12	chr4:1161157-1161207	HAEpiC	amniotic membrane:	n/a
13	chr4:1161157-1161207	SAEC	small airway:	n/a
14	chr4:1161157-1161207	HMEC	breast:	n/a
15	chr4:1161157-1161207	GM06990	blood:	n/a
16	chr4:1161157-1161207	ovcar-3	ovarian:	n/a
17	chr4:1161157-1161207	IMR90	lung:	fetal
18	chr4:1161157-1161207	HEEpiC	esophagus:	n/a
19	chr4:1161157-1161207	AG04449	skin:	fetal
20	chr4:1161157-1161207	ECC-1	luminal epithelium:	n/a
21	chr4:1161157-1161207	BE2_C	brain:	n/a
22	chr4:1161157-1161207	Caco-2	colon:	n/a
23	chr4:1161157-1161207	SK-N-MC	brain:	n/a
24	chr4:1161157-1161207	MCF-7	breast:	n/a
25	chr4:1161157-1161207	Hela-S3	cervix:	n/a
26	chr4:1161157-1161207	NB4	blood:	n/a
27	chr4:1161157-1161207	GM12878	blood:	n/a
28	chr4:1161157-1161207	HUVEC	blood vessel:	n/a
29	chr4:1161157-1161207	HepG2	liver:	n/a
30	chr4:1161157-1161207	GM19239	blood:	n/a
31	chr4:1161157-1161207	AG10803	skin:	n/a
32	chr4:1161157-1161207	HRE	kidney:	n/a
33	chr4:1161157-1161207	T-47D	breast:	n/a
34	chr4:1161157-1161207	AG09319	gingival:	n/a
35	chr4:1161157-1161207	AG04450	lung:	fetal
36	chr4:1161157-1161207	GM12892	blood:	n/a
37	chr4:1161157-1161207	NT2-D1	testis:	n/a
38	chr4:1161157-1161207	HCPEpiC	choroid plexus:	n/a
39	chr4:1161157-1161207	HNPCEpiC	eye:	n/a
40	chr4:1161157-1161207	K562	blood:	n/a
41	chr4:1161157-1161207	PFSK-1	brain:	n/a
42	chr4:1161157-1161207	AoSMC	blood vessel:	n/a
43	chr4:1161157-1161207	LNCaP	prostate:	n/a
44	chr4:1161157-1161207	NH-A	brain:	n/a
45	chr4:1161157-1161207	NHDF-neo	bronchial:	n/a
46	chr4:1161157-1161207	PrEC	prostate:	n/a
47	chr4:1161157-1161207	SK-N-SH	brain:	n/a
48	chr4:1161157-1161207	AG09309	skin:	n/a
49	chr4:1161157-1161207	HEK293	kidney:	embryo
50	chr4:1161157-1161207	Jurkat	blood:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:1148836..1150656-chr4:1158742..1161485,3	K562	blood:
2	chr4:1161114..1165211-chr4:1166165..1170804,4	MCF-7	breast:
3	chr4:1160646..1161190-chr4:1630954..1631559,2	K562	blood:
4	chr4:1159939..1161445-chr4:1340149..1342873,2	MCF-7	breast:
5	chr19:2269356..2269867-chr4:1160687..1161536,2	NB4	blood:
6	chr4:1124107..1124994-chr4:1160647..1161547,3	K562	blood:
7	chr4:1157936..1161506-chr4:1282339..1285236,6	K562	blood:
8	chr4:1159229..1162099-chr4:1242725..1245069,2	K562	blood:
9	chr4:1159882..1162594-chr4:1225934..1228487,2	MCF-7	breast:
10	chr4:1158166..1163360-chr4:1238498..1245354,13	MCF-7	breast:
11	chr4:1160924..1165328-chr4:1340425..1343058,5	MCF-7	breast:
12	chr4:1160724..1161481-chr4:1208619..1209214,2	K562	blood:
13	chr4:1161085..1161655-chrX:63425593..63426536,2	NB4	blood:
14	chr4:1146501..1148469-chr4:1159921..1162668,2	MCF-7	breast:
15	chr4:1160471..1164177-chr4:1164804..1166602,3	K562	blood:
16	chr4:1159479..1162008-chr4:1166717..1168665,3	MCF-7	breast:
17	chr4:1159747..1163015-chr4:1240558..1244483,3	K562	blood:
18	chr4:1159320..1162756-chr4:1282339..1286135,5	K562	blood:

No data

Variant related genes	Relation type
ENSG00000273179	TF binding region
ENSG00000273179	CpG island
ENSG00000159674	Chromatin interaction
ENSG00000215367	Chromatin interaction
ENSG00000184675	Chromatin interaction
ENSG00000090316	Chromatin interaction
ENSG00000196810	Chromatin interaction
ENSG00000159692	Chromatin interaction
ENSG00000104904	Chromatin interaction
ENSG00000167476	Chromatin interaction
ENSG00000163945	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10003030	1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs10016588	0.86[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs11723211	0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11726675	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11726836	0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11731643	0.92[ASN][1000 genomes]
rs11735226	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17164362	0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17164373	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2001862	0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28540372	0.95[ASN][1000 genomes]
rs3775110	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3775111	1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs6831018	0.88[ASN][1000 genomes]
rs6853712	0.88[ASN][1000 genomes]
rs7659054	0.86[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs7661069	0.86[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs7669287	0.86[CHB][hapmap];1.00[JPT][hapmap];0.95[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	nsv822425	chr4:540105-1413799	Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	108 gene(s)	inside rSNPs	diseases
2	nsv530490	chr4:614355-1399150	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
3	nsv536980	chr4:827866-1167377	Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
4	nsv1009619	chr4:901897-1215657	Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
5	nsv1003876	chr4:927509-1191316	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
6	nsv1000381	chr4:927509-1198766	Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
7	esv3339080	chr4:970630-1546223	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription 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 miRNA target site	82 gene(s)	inside rSNPs	diseases
8	nsv1005990	chr4:1015652-1167619	Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
9	nsv1012892	chr4:1086871-1176630	Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
10	nsv829835	chr4:1097586-1304239	Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
11	nsv878328	chr4:1141573-1990425	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	121 gene(s)	inside rSNPs	diseases
12	nsv878329	chr4:1147407-1254930	Genic enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
13	nsv878330	chr4:1147407-1523930	Strong transcription Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
14	nsv519106	chr4:1158991-1174861	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
15	nsv593276	chr4:1159680-1227469	Flanking Active TSS Genic enhancers Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
16	nsv461151	chr4:1159680-1236840	Enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
17	nsv593277	chr4:1159680-1236840	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
18	nsv878331	chr4:1159680-1254930	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
19	nsv461152	chr4:1159680-1415698	Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
20	nsv593278	chr4:1159680-1415698	Enhancers Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	70 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	chr4:1160000-1161200	Strong transcription	NHLF	lung
2	chr4:1160400-1163400	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr4:1160600-1161200	Flanking Active TSS	Dnd41	blood
4	chr4:1160600-1162000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr4:1160800-1161200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr4:1160800-1161200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr4:1160800-1161200	Flanking Active TSS	Primary B cells from peripheral blood	blood
8	chr4:1160800-1161200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
9	chr4:1160800-1161200	Enhancers	Brain Angular Gyrus	brain
10	chr4:1160800-1161200	Enhancers	Fetal Brain Male	brain
11	chr4:1160800-1161200	Enhancers	Fetal Lung	lung
12	chr4:1160800-1161200	Enhancers	Ovary	ovary
13	chr4:1160800-1161200	Enhancers	Stomach Mucosa	stomach
14	chr4:1160800-1161200	Enhancers	NHDF-Ad	bronchial
15	chr4:1160800-1161400	Active TSS	Duodenum Smooth Muscle	Duodenum
16	chr4:1160800-1161400	Enhancers	Fetal Heart	heart
17	chr4:1160800-1161600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr4:1160800-1161600	Active TSS	Brain Cingulate Gyrus	brain
19	chr4:1160800-1161600	Bivalent/Poised TSS	Brain Germinal Matrix	brain
20	chr4:1160800-1161800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
21	chr4:1160800-1161800	Active TSS	H9 Cell Line	embryonic stem cell
22	chr4:1160800-1161800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
23	chr4:1160800-1161800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
24	chr4:1160800-1161800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr4:1160800-1161800	Active TSS	Rectal Smooth Muscle	rectum
26	chr4:1160800-1162000	Flanking Active TSS	Primary B cells from cord blood	blood
27	chr4:1160800-1162000	Flanking Active TSS	Liver	Liver
28	chr4:1160800-1162000	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
29	chr4:1161000-1161200	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
30	chr4:1161000-1161200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr4:1161000-1161200	Active TSS	Breast Myoepithelial Primary Cells	Breast
32	chr4:1161000-1161200	Active TSS	Primary neutrophils fromperipheralblood	blood
33	chr4:1161000-1161200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
34	chr4:1161000-1161200	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
35	chr4:1161000-1161200	Active TSS	Muscle Satellite Cultured Cells	--
36	chr4:1161000-1161200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr4:1161000-1161200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr4:1161000-1161200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr4:1161000-1161200	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
40	chr4:1161000-1161200	Active TSS	Colonic Mucosa	Colon
41	chr4:1161000-1161200	Enhancers	Pancreas	Pancrea
42	chr4:1161000-1161200	Active TSS	Rectal Mucosa Donor 29	rectum
43	chr4:1161000-1161200	Active TSS	Skeletal Muscle Female	skeletal muscle
44	chr4:1161000-1161200	Active TSS	Stomach Smooth Muscle	stomach
45	chr4:1161000-1161200	Active TSS	GM12878-XiMat	blood
46	chr4:1161000-1161200	Active TSS	HUVEC	blood vessel
47	chr4:1161000-1161200	Active TSS	Monocytes-CD14+_RO01746	blood
48	chr4:1161000-1161200	Active TSS	NH-A	brain
49	chr4:1161000-1161400	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr4:1161000-1161400	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell

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