Variant report

Variant	rs567442107
Chromosome Location	chr4:128981488-128981489
allele	-/A
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:25)
CpG islands
(count:61)
Chromatin interactive
region (count:18)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr4:128981341-128983767	GM12878	blood:	n/a	n/a
2	E2F4	chr4:128981415-128982595	MCF10A-Er-Src	breast:	n/a	chr4:128981810-128981819 chr4:128982158-128982168 chr4:128981810-128981822 chr4:128981966-128981976
3	MYC	chr4:128981397-128983701	K562	blood:	n/a	chr4:128982117-128982126 chr4:128982024-128982034 chr4:128983439-128983448 chr4:128983126-128983135 chr4:128982117-128982127
4	POLR2A	chr4:128981211-128982633	K562	blood:	n/a	n/a
5	MAX	chr4:128981302-128983662	K562	blood:	n/a	chr4:128982117-128982126 chr4:128982024-128982034 chr4:128983439-128983448 chr4:128983126-128983135 chr4:128982117-128982127
6	POLR2A	chr4:128981401-128982868	K562	blood:	n/a	n/a
7	POLR2A	chr4:128981306-128981654	GM12892	blood:	n/a	n/a
8	POLR2A	chr4:128981458-128983146	HepG2	liver:	n/a	n/a
9	MXI1	chr4:128981232-128984296	SK-N-SH	brain:	n/a	n/a
10	POLR2A	chr4:128981181-128983788	MCF10A-Er-Src	breast:	n/a	n/a
11	MYC	chr4:128981449-128984203	K562	blood:	n/a	chr4:128982117-128982126 chr4:128982024-128982034 chr4:128983439-128983448 chr4:128983126-128983135 chr4:128982117-128982127
12	POLR2A	chr4:128981454-128983658	K562	blood:	n/a	n/a
13	POLR2A	chr4:128981387-128983772	HL-60	blood:	n/a	n/a
14	POLR2A	chr4:128981448-128983594	K562	blood:	n/a	n/a
15	POLR2A	chr4:128981161-128983751	HepG2	liver:	n/a	n/a
16	JUND	chr4:128981347-128982986	K562	blood:	n/a	n/a
17	POLR2A	chr4:128981431-128983738	GM18505	blood:	n/a	n/a
18	POLR2A	chr4:128981078-128983720	MCF10A-Er-Src	breast:	n/a	n/a
19	POLR2A	chr4:128981130-128982715	GM12891	blood:	n/a	n/a
20	POLR2A	chr4:128981181-128983644	IMR90	lung:	n/a	n/a
21	POLR2A	chr4:128981433-128983744	Hela-S3	cervix:	n/a	n/a
22	MAZ	chr4:128981378-128983733	K562	blood:	n/a	chr4:128982117-128982126 chr4:128982024-128982034 chr4:128983439-128983448 chr4:128983126-128983135
23	IRF1	chr4:128981365-128981744	K562	blood:	n/a	chr4:128981549-128981566 chr4:128981550-128981561 chr4:128981549-128981561 chr4:128981546-128981560 chr4:128981550-128981560
24	POLR2A	chr4:128981467-128983627	H1-hESC	embryonic stem cell:	n/a	n/a
25	GTF2B	chr4:128981425-128982567	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:128981486-128981536	HEEpiC	esophagus:	n/a
2	chr4:128981486-128981536	AG04450	lung:	fetal
3	chr4:128981486-128981536	MCF10A-Er-Src	breast:	n/a
4	chr4:128981486-128981536	AG04449	skin:	fetal
5	chr4:128981486-128981536	CMK	blood:	n/a
6	chr4:128981486-128981536	HCF	heart:	n/a
7	chr4:128981486-128981536	HMEC	breast:	n/a
8	chr4:128981486-128981536	BE2_C	brain:	n/a
9	chr4:128981486-128981536	LNCaP	prostate:	n/a
10	chr4:128981486-128981536	HRPEpiC	eye:	n/a
11	chr4:128981486-128981536	HIPEpiC	eye:	n/a
12	chr4:128981486-128981536	SKMC	muscle:	n/a
13	chr4:128981486-128981536	HUVEC	blood vessel:	n/a
14	chr4:128981486-128981536	IMR90	lung:	fetal
15	chr4:128981486-128981536	NH-A	brain:	n/a
16	chr4:128981486-128981536	U87	brain:	n/a
17	chr4:128981486-128981536	BJ	skin:	n/a
18	chr4:128981486-128981536	HAEpiC	amniotic membrane:	n/a
19	chr4:128981486-128981536	PrEC	prostate:	n/a
20	chr4:128981486-128981536	MCF-7	breast:	n/a
21	chr4:128981486-128981536	HNPCEpiC	eye:	n/a
22	chr4:128981486-128981536	GM12892	blood:	n/a
23	chr4:128981486-128981536	GM06990	blood:	n/a
24	chr4:128981486-128981536	K562	blood:	n/a
25	chr4:128981486-128981536	GM19239	blood:	n/a
26	chr4:128981486-128981536	Hepatocyte	liver:	n/a
27	chr4:128981486-128981536	SAEC	small airway:	n/a
28	chr4:128981486-128981536	A549	lung:	n/a
29	chr4:128981486-128981536	T-47D	breast:	n/a
30	chr4:128981486-128981536	AG09319	gingival:	n/a
31	chr4:128981486-128981536	NHDF-neo	bronchial:	n/a
32	chr4:128981486-128981536	HCT-116	colon:	n/a
33	chr4:128981486-128981536	GM12878	blood:	n/a
34	chr4:128981486-128981536	NT2-D1	testis:	n/a
35	chr4:128981486-128981536	HRE	kidney:	n/a
36	chr4:128981486-128981536	AoSMC	blood vessel:	n/a
37	chr4:128981486-128981536	HCPEpiC	choroid plexus:	n/a
38	chr4:128981486-128981536	RPTEC	kidney:	n/a
39	chr4:128981486-128981536	Caco-2	colon:	n/a
40	chr4:128981486-128981536	GM12891	blood:	n/a
41	chr4:128981486-128981536	Hela-S3	cervix:	n/a
42	chr4:128981486-128981536	AG10803	skin:	n/a
43	chr4:128981486-128981536	ECC-1	luminal epithelium:	n/a
44	chr4:128981486-128981536	SK-N-MC	brain:	n/a
45	chr4:128981486-128981536	HRCEpiC	kidney:	n/a
46	chr4:128981486-128981536	ovcar-3	ovarian:	n/a
47	chr4:128981486-128981536	HL-60	blood:	n/a
48	chr4:128981486-128981536	PFSK-1	brain:	n/a
49	chr4:128981486-128981536	SK-N-SH_RA	brain:	n/a
50	chr4:128981486-128981536	ProgFib	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:128894792..128897559-chr4:128980082..128981594,2	K562	blood:
2	chr4:128981378..128983346-chr4:128988931..128991317,2	MCF-7	breast:
3	chr4:128884518..128888041-chr4:128980422..128985043,7	MCF-7	breast:
4	chr4:128800019..128803742-chr4:128979765..128984325,9	K562	blood:
5	chr4:128885127..128890546-chr4:128980550..128983845,11	K562	blood:
6	chr4:128980795..128982891-chr4:129730267..129732892,3	K562	blood:
7	chr4:128980795..128984031-chr4:129730059..129735028,7	K562	blood:
8	chr4:128701934..128705815-chr4:128979420..128985014,7	K562	blood:
9	chr4:128884064..128888795-chr4:128980591..128984632,7	MCF-7	breast:
10	chr4:128701934..128705815-chr4:128979420..128984468,5	K562	blood:
11	chr4:128980817..128984026-chr4:129207052..129210590,3	MCF-7	breast:
12	chr4:128980866..128984600-chr4:128984636..128991176,13	K562	blood:
13	chr4:128980667..128982380-chr4:129732444..129734327,2	MCF-7	breast:
14	chr4:128702147..128704685-chr4:128980177..128982661,2	MCF-7	breast:
15	chr4:128980375..128984020-chr4:128989687..128993521,7	MCF-7	breast:
16	chr11:61129378..61130089-chr4:128981023..128981777,2	Hela-S3	cervix:
17	chr4:128884948..128891801-chr4:128980633..128984811,17	K562	blood:
18	chr4:128800672..128803742-chr4:128979765..128985676,12	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MFSD8-7	chr4:128981059-128981632	NONHSAT098254

No data

Variant related genes	Relation type
LARP1B	TF binding region
LARP1B	CpG island
ENSG00000241651	Chromatin interaction
ENSG00000164070	Chromatin interaction
ENSG00000142731	Chromatin interaction
ENSG00000077684	Chromatin interaction
ENSG00000164073	Chromatin interaction
ENSG00000149483	Chromatin interaction
ENSG00000164040	Chromatin interaction
ENSG00000162144	Chromatin interaction
ENSG00000164074	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:31 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv879915	chr4:128167093-129150590	Strong transcription Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking 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	48 gene(s)	inside rSNPs	diseases
2	nsv879923	chr4:128554404-129068179	Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
3	esv1792644	chr4:128566686-129133826	Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
4	esv1795770	chr4:128566686-129145581	Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS Weak transcription Genic enhancers Enhancers ZNF genes & repeats 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	44 gene(s)	inside rSNPs	diseases
5	nsv532740	chr4:128710011-129035335	Weak transcription Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
6	esv3416036	chr4:128782694-129133956	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
7	nsv1033701	chr4:128803159-129095018	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
8	esv1841203	chr4:128817558-129043809	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers 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	29 gene(s)	inside rSNPs	diseases
9	nsv1029890	chr4:128828468-129041302	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Genic enhancers 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	28 gene(s)	inside rSNPs	diseases
10	esv1817670	chr4:128850073-129012181	Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
11	esv1821180	chr4:128850073-129012181	Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh 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
12	nsv1018952	chr4:128850790-129082821	Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
13	nsv595388	chr4:128853913-129084831	Weak transcription Active TSS Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
14	nsv1019555	chr4:128901614-129088903	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Active TSS 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	25 gene(s)	inside rSNPs	diseases
15	esv3390887	chr4:128932563-129207255	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers 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 target site	25 gene(s)	inside rSNPs	diseases
16	esv1800378	chr4:128954647-128986874	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
17	esv1801389	chr4:128954647-128986874	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
18	esv1802601	chr4:128954647-128986874	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
19	esv3353674	chr4:128958396-128983454	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
20	esv3430549	chr4:128958396-128987680	Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
21	esv3385008	chr4:128959396-128991050	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
22	esv1795256	chr4:128960569-128983211	Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
23	esv1797884	chr4:128960569-128983211	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
24	esv1800439	chr4:128972357-128986874	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
25	esv1800138	chr4:128981336-128983211	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
26	esv1803700	chr4:128981336-128983211	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
27	esv1836544	chr4:128981336-128983211	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
28	esv1838939	chr4:128981336-128983211	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
29	esv1802578	chr4:128981336-128986874	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
30	esv1836174	chr4:128981336-128995640	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
31	esv1837247	chr4:128981336-128995640	Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:128951400-128981800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr4:128980200-128981800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr4:128981000-128981600	Flanking Active TSS	Dnd41	blood
4	chr4:128981000-128982800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr4:128981000-128983200	Active TSS	Rectal Mucosa Donor 29	rectum
6	chr4:128981000-128983600	Active TSS	Liver	Liver
7	chr4:128981000-128983800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr4:128981000-128984400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr4:128981000-128984400	Active TSS	Duodenum Mucosa	Duodenum
10	chr4:128981000-128984400	Active TSS	Pancreatic Islets	Pancreatic Islet
11	chr4:128981000-128984400	Active TSS	Rectal Smooth Muscle	rectum
12	chr4:128981200-128981600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
13	chr4:128981200-128981600	Enhancers	Primary B cells from peripheral blood	blood
14	chr4:128981200-128981600	Enhancers	Primary T helper cells fromperipheralblood	blood
15	chr4:128981200-128981600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr4:128981200-128981600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
17	chr4:128981200-128981600	Enhancers	Fetal Heart	heart
18	chr4:128981200-128981600	Flanking Active TSS	Placenta	Placenta
19	chr4:128981200-128981600	Active TSS	Stomach Smooth Muscle	stomach
20	chr4:128981200-128981600	Flanking Active TSS	A549	lung
21	chr4:128981200-128981600	Flanking Active TSS	HMEC	breast
22	chr4:128981200-128981600	Flanking Active TSS	K562	blood
23	chr4:128981200-128981800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
24	chr4:128981200-128981800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr4:128981200-128981800	Flanking Active TSS	Adipose Nuclei	Adipose
26	chr4:128981200-128981800	Flanking Active TSS	Hela-S3	cervix
27	chr4:128981200-128982000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
28	chr4:128981200-128982200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr4:128981200-128982200	Active TSS	Stomach Mucosa	stomach
30	chr4:128981200-128983200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
31	chr4:128981200-128983400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr4:128981200-128983600	Active TSS	Primary T killer memory cells from peripheral blood	blood
33	chr4:128981200-128983600	Active TSS	Colon Smooth Muscle	Colon
34	chr4:128981200-128983600	Active TSS	Osteobl	bone
35	chr4:128981200-128983800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr4:128981200-128983800	Active TSS	Brain Hippocampus Middle	brain
37	chr4:128981200-128983800	Active TSS	Psoas Muscle	Psoas
38	chr4:128981200-128984000	Active TSS	Duodenum Smooth Muscle	Duodenum
39	chr4:128981200-128984000	Active TSS	NHEK	skin
40	chr4:128981200-128984200	Active TSS	Brain Angular Gyrus	brain
41	chr4:128981200-128984200	Active TSS	Fetal Intestine Large	intestine
42	chr4:128981200-128984200	Active TSS	GM12878-XiMat	blood
43	chr4:128981200-128984400	Active TSS	ES-I3 Cell Line	embryonic stem cell
44	chr4:128981200-128984400	Active TSS	HUES64 Cell Line	embryonic stem cell
45	chr4:128981200-128984400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr4:128981200-128984400	Active TSS	Fetal Intestine Small	intestine
47	chr4:128981200-128984400	Active TSS	Fetal Kidney	kidney
48	chr4:128981200-128984400	Active TSS	Fetal Stomach	stomach
49	chr4:128981200-128984400	Active TSS	Rectal Mucosa Donor 31	rectum
50	chr4:128981400-128981600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell

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