Variant report

Variant	rs28732141
Chromosome Location	chr6:31519365-31519366
allele	C/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	CTCF	chr6:31519180-31519445	K562	blood:	n/a	chr6:31519310-31519328 chr6:31519312-31519333
2	RAD21	chr6:31519156-31519473	HepG2	liver:	n/a	chr6:31519311-31519330
3	SMC3	chr6:31519151-31519493	K562	blood:	n/a	chr6:31519312-31519319 chr6:31519312-31519326
4	CTCF	chr6:31519220-31519370	GM12801	blood:	n/a	chr6:31519310-31519328 chr6:31519312-31519333
5	CTCF	chr6:31519260-31519410	GM12865	blood:	n/a	chr6:31519310-31519328 chr6:31519312-31519333
6	CTCF	chr6:31519240-31519390	HL-60	blood:	n/a	chr6:31519310-31519328 chr6:31519312-31519333
7	CTCF	chr6:31519240-31519390	GM12869	blood:	n/a	chr6:31519310-31519328 chr6:31519312-31519333
8	CTCF	chr6:31519193-31519416	A549	lung:	n/a	chr6:31519310-31519328 chr6:31519312-31519333
9	CTCF	chr6:31519192-31519441	K562	blood:	n/a	chr6:31519310-31519328 chr6:31519312-31519333
10	CTCF	chr6:31519220-31519370	AG09309	skin:	n/a	chr6:31519310-31519328 chr6:31519312-31519333
11	SMC3	chr6:31519161-31519479	HepG2	liver:	n/a	chr6:31519312-31519319 chr6:31519312-31519326
12	RAD21	chr6:31519149-31519479	K562	blood:	n/a	chr6:31519311-31519330
13	CTCF	chr6:31519165-31519448	GM12892	blood:	n/a	chr6:31519310-31519328 chr6:31519312-31519333
14	RAD21	chr6:31519081-31519458	A549	lung:	n/a	chr6:31519311-31519330
15	CTCF	chr6:31519220-31519370	HCFaa	heart:	n/a	chr6:31519310-31519328 chr6:31519312-31519333
16	CTCF	chr6:31519221-31519413	Pancreas_OC	pancreas:	n/a	chr6:31519310-31519328 chr6:31519312-31519333
17	PML	chr6:31519086-31519609	GM12878	blood:	n/a	n/a
18	CTCF	chr6:31519240-31519390	GM12873	blood:	n/a	chr6:31519310-31519328 chr6:31519312-31519333
19	CTCF	chr6:31519141-31519496	A549	lung:	n/a	chr6:31519310-31519328 chr6:31519312-31519333
20	CTCF	chr6:31519222-31519420	A549	lung:	n/a	chr6:31519310-31519328 chr6:31519312-31519333
21	CTCF	chr6:31519191-31519421	MCF-7	breast:	n/a	chr6:31519310-31519328 chr6:31519312-31519333
22	CTCF	chr6:31519280-31519430	HAc	cerebellar:	n/a	chr6:31519310-31519328 chr6:31519312-31519333
23	BCLAF1	chr6:31519095-31519436	GM12878	blood:	n/a	n/a
24	RAD21	chr6:31519151-31519508	Hela-S3	cervix:	n/a	chr6:31519311-31519330
25	RAD21	chr6:31519012-31519565	MCF-7	breast:	n/a	chr6:31519311-31519330
26	CTCF	chr6:31519222-31519394	NHEK	skin:	n/a	chr6:31519310-31519328 chr6:31519312-31519333
27	CTCF	chr6:31519190-31519431	GM13977	blood:	n/a	chr6:31519310-31519328 chr6:31519312-31519333
28	FOXM1	chr6:31519050-31519540	GM12878	blood:	n/a	n/a
29	CTCF	chr6:31519176-31519451	MCF-7	breast:	n/a	chr6:31519310-31519328 chr6:31519312-31519333
30	CTCF	chr6:31519173-31519438	HUVEC	blood vessel:	n/a	chr6:31519310-31519328 chr6:31519312-31519333
31	CTCF	chr6:31519220-31519370	GM12874	blood:	n/a	chr6:31519310-31519328 chr6:31519312-31519333
32	CTCF	chr6:31519138-31519468	Spleen_OC	spleen:	n/a	chr6:31519310-31519328 chr6:31519312-31519333
33	CTCF	chr6:31519219-31519416	HepG2	liver:	n/a	chr6:31519310-31519328 chr6:31519312-31519333
34	FOXA1	chr6:31519144-31519427	T-47D	breast:	n/a	n/a
35	CTCF	chr6:31519211-31519415	Hela-S3	cervix:	n/a	chr6:31519310-31519328 chr6:31519312-31519333
36	CTCF	chr6:31519235-31519415	Medullo	brain:	n/a	chr6:31519310-31519328 chr6:31519312-31519333
37	RAD21	chr6:31519158-31519430	K562	blood:	n/a	chr6:31519311-31519330
38	ZNF143	chr6:31519259-31519446	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr6:31519115-31519486	K562	blood:	n/a	chr6:31519310-31519328 chr6:31519312-31519333
40	RAD21	chr6:31519073-31519529	HepG2	liver:	n/a	chr6:31519311-31519330
41	FOXA1	chr6:31518995-31519403	HepG2	liver:	n/a	n/a
42	CTCF	chr6:31519162-31519444	Lung_OC	lung:	n/a	chr6:31519310-31519328 chr6:31519312-31519333
43	RAD21	chr6:31519157-31519471	A549	lung:	n/a	chr6:31519311-31519330
44	RAD21	chr6:31519147-31519505	IMR90	lung:	n/a	chr6:31519311-31519330
45	RAD21	chr6:31519095-31519457	H1-hESC	embryonic stem cell:	n/a	chr6:31519311-31519330
46	CTCF	chr6:31519240-31519390	GM12870	blood:	n/a	chr6:31519310-31519328 chr6:31519312-31519333
47	RAD21	chr6:31519159-31519422	K562	blood:	n/a	chr6:31519311-31519330
48	ARID3A	chr6:31519208-31519408	K562	blood:	n/a	n/a
49	MAZ	chr6:31519260-31519398	K562	blood:	n/a	n/a
50	CTCF	chr6:31519260-31519410	HA-sp	spinal cord:	n/a	chr6:31519310-31519328 chr6:31519312-31519333

No.	Distal block	Cell Line	Cell type
1	chr6:31518769..31519842-chr6:31566031..31567026,10	K562	blood:
2	chr6:31517592..31522537-chr6:31564964..31567939,4	MCF-7	breast:
3	chr6:31519244..31520760-chr6:31592464..31593989,2	K562	blood:
4	chr6:31513079..31516854-chr6:31518993..31522440,4	K562	blood:
5	chr6:31518891..31519744-chr6:31548336..31548887,2	K562	blood:
6	chr6:31519280..31519781-chr6:31553143..31553855,2	MCF-7	breast:
7	chr6:31518830..31519751-chr6:31564938..31565442,2	MCF-7	breast:
8	chr6:31519028..31519735-chr6:31566077..31566659,3	MCF-7	breast:
9	chr6:31518175..31519881-chr6:31566042..31567461,7	MCF-7	breast:
10	chr6:31509907..31511737-chr6:31518238..31520008,2	MCF-7	breast:
11	chr6:31515650..31517659-chr6:31517852..31520397,2	MCF-7	breast:

Variant related genes	Relation type
ATP6V1G2	TF binding region
ATP6V1G2-DDX39B	TF binding region
ENSG00000234006	Chromatin interaction
ENSG00000198563	Chromatin interaction
ENSG00000204498	Chromatin interaction
ENSG00000213760	Chromatin interaction
ENSG00000204469	Chromatin interaction
ENSG00000254870	Chromatin interaction

Extended variants
information (count: 61 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs17207190	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2516474	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28381344	0.83[AMR][1000 genomes]
rs28732142	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28732143	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28732144	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28732145	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs28732153	0.83[AMR][1000 genomes]
rs28732155	0.83[AMR][1000 genomes]
rs28732156	0.83[AMR][1000 genomes]
rs28732159	0.83[AMR][1000 genomes]
rs28732160	0.83[AMR][1000 genomes]
rs28895015	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2905741	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs3021366	1.00[ASN][1000 genomes]
rs3093661	0.98[EUR][1000 genomes]
rs3093668	1.00[EUR][1000 genomes]
rs3093726	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3093727	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs361525	0.81[EUR][1000 genomes]
rs3828917	0.83[EUR][1000 genomes]
rs41293856	0.83[EUR][1000 genomes]
rs41293860	0.83[EUR][1000 genomes]
rs41293879	0.83[EUR][1000 genomes]
rs41293887	0.88[EUR][1000 genomes]
rs41293891	0.84[EUR][1000 genomes]
rs41293895	0.93[EUR][1000 genomes]
rs41293899	0.93[EUR][1000 genomes]
rs41293907	0.93[EUR][1000 genomes]
rs41293911	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41293915	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs41293919	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41293923	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs41315808	0.83[AMR][1000 genomes]
rs4947326	0.85[EUR][1000 genomes]
rs4947327	0.85[EUR][1000 genomes]
rs4959077	0.88[EUR][1000 genomes]
rs4959078	0.93[EUR][1000 genomes]
rs7757162	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7757383	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9267497	0.85[EUR][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	nsv1015372	chr6:30704734-31582152	Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
2	nsv538173	chr6:30704734-31582152	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
3	esv2759414	chr6:31028290-31542308	Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	151 gene(s)	inside rSNPs	diseases
4	nsv601609	chr6:31280101-31799786	Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers Genic enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	332 gene(s)	inside rSNPs	diseases
5	nsv601610	chr6:31280101-31960770	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	370 gene(s)	inside rSNPs	diseases
6	nsv601628	chr6:31280327-31990098	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
7	nsv601629	chr6:31280327-31996185	Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer 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	376 gene(s)	inside rSNPs	diseases
8	nsv601630	chr6:31280327-32011317	Genic enhancers Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer 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	378 gene(s)	inside rSNPs	diseases
9	nsv601631	chr6:31280327-32017540	Genic enhancers Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer 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	378 gene(s)	inside rSNPs	diseases
10	nsv1023939	chr6:31325961-32026747	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	372 gene(s)	inside rSNPs	diseases
11	nsv538188	chr6:31325961-32026747	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	372 gene(s)	inside rSNPs	diseases
12	nsv1018463	chr6:31337336-31525275	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	104 gene(s)	inside rSNPs	diseases
13	nsv538189	chr6:31337336-31525275	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	104 gene(s)	inside rSNPs	diseases
14	nsv432868	chr6:31338844-31721033	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	250 gene(s)	inside rSNPs	diseases
15	esv2757162	chr6:31353329-31542308	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	99 gene(s)	inside rSNPs	diseases
16	nsv1021747	chr6:31386219-31907266	Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	330 gene(s)	inside rSNPs	diseases
17	nsv432877	chr6:31412961-31528690	Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	88 gene(s)	inside rSNPs	diseases
18	nsv830627	chr6:31496214-31659950	Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Genic enhancers Enhancers Strong transcription Active TSS 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	182 gene(s)	inside rSNPs	diseases
19	nsv470809	chr6:31496915-31544189	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers 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	76 gene(s)	inside rSNPs	diseases
20	nsv884417	chr6:31515078-31525354	Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs28732141	MICB	Cis_1M	lymphoblastoid	RTeQTL
rs28732141	XXbac-BPG181B23.7	cis	Whole Blood	GTEx
rs28732141	MICA///MICB	N/A	lymphoblastoid	RTeQTL
rs28732141	MICB	cis	Whole Blood	GTEx
rs28732141	MICB	cis	Adipose Subcutaneous	GTEx

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31515600-31525400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr6:31515600-31525600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr6:31516000-31526400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr6:31516000-31535800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr6:31516200-31522400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
6	chr6:31516200-31525800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr6:31516400-31519400	Strong transcription	Fetal Muscle Trunk	muscle
8	chr6:31516400-31522000	Weak transcription	Esophagus	oesophagus
9	chr6:31516400-31522800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr6:31516400-31523600	Weak transcription	Primary hematopoietic stem cells	blood
11	chr6:31516400-31523800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr6:31516400-31523800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr6:31516400-31523800	Weak transcription	Ovary	ovary
14	chr6:31516400-31523800	Weak transcription	Pancreas	Pancrea
15	chr6:31516400-31525400	Weak transcription	Right Atrium	heart
16	chr6:31516400-31526200	Weak transcription	Small Intestine	intestine
17	chr6:31516400-31526200	Weak transcription	NH-A	brain
18	chr6:31516400-31526200	Weak transcription	NHDF-Ad	bronchial
19	chr6:31516400-31526400	Weak transcription	A549	lung
20	chr6:31516400-31526600	Weak transcription	Psoas Muscle	Psoas
21	chr6:31516400-31527200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr6:31516400-31533200	Weak transcription	Fetal Brain Male	brain
23	chr6:31516600-31521000	Weak transcription	HSMMtube	muscle
24	chr6:31516600-31521800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr6:31516600-31522200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr6:31516600-31522400	Strong transcription	Fetal Intestine Small	intestine
27	chr6:31516600-31523800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr6:31516600-31523800	Weak transcription	Spleen	Spleen
29	chr6:31516600-31525200	Strong transcription	Fetal Muscle Leg	muscle
30	chr6:31516600-31529200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr6:31516800-31519400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr6:31516800-31519400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr6:31516800-31519400	Strong transcription	Rectal Mucosa Donor 29	rectum
34	chr6:31516800-31520000	Strong transcription	Liver	Liver
35	chr6:31516800-31520400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr6:31516800-31522200	Strong transcription	Fetal Stomach	stomach
37	chr6:31516800-31523800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
38	chr6:31516800-31523800	Weak transcription	Brain Cingulate Gyrus	brain
39	chr6:31516800-31523800	Weak transcription	Duodenum Smooth Muscle	Duodenum
40	chr6:31516800-31523800	Weak transcription	HUVEC	blood vessel
41	chr6:31516800-31530800	Weak transcription	Stomach Mucosa	stomach
42	chr6:31516800-31531000	Weak transcription	Fetal Kidney	kidney
43	chr6:31517000-31519400	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
44	chr6:31517000-31519400	Strong transcription	Duodenum Mucosa	Duodenum
45	chr6:31517000-31519400	Strong transcription	Stomach Smooth Muscle	stomach
46	chr6:31517000-31519600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
47	chr6:31517000-31520000	Strong transcription	Fetal Brain Female	brain
48	chr6:31517000-31520400	Strong transcription	K562	blood
49	chr6:31517000-31522000	Strong transcription	Osteobl	bone
50	chr6:31517000-31523600	Weak transcription	Brain Substantia Nigra	brain

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