Variant report

Variant	rs11012731
Chromosome Location	chr10:21816590-21816591
allele	A/C
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	TBL1XR1	chr10:21816386-21817361	K562	blood:	n/a	n/a
2	GATA3	chr10:21816566-21816802	SH-SY5Y	brain:	n/a	chr10:21816578-21816585 chr10:21816578-21816585 chr10:21816578-21816589 chr10:21816573-21816589 chr10:21816578-21816585 chr10:21816571-21816592
3	MYC	chr10:21814313-21817222	MCF10A-Er-Src	breast:	n/a	chr10:21816323-21816333 chr10:21815247-21815257 chr10:21816880-21816888 chr10:21814827-21814836
4	CHD1	chr10:21812350-21818489	H1-hESC	embryonic stem cell:	n/a	chr10:21815540-21815550 chr10:21814991-21815001
5	MAX	chr10:21814041-21817178	SK-N-SH	brain:	n/a	chr10:21816323-21816333 chr10:21815247-21815257 chr10:21816880-21816888 chr10:21814827-21814836
6	MYC	chr10:21812479-21817071	K562	blood:	n/a	chr10:21816323-21816333 chr10:21815247-21815257 chr10:21816880-21816888 chr10:21814827-21814836 chr10:21813519-21813529
7	TBP	chr10:21813474-21817455	K562	blood:	n/a	n/a
8	MAFK	chr10:21816527-21816922	HepG2	liver:	n/a	chr10:21816732-21816748 chr10:21816730-21816750
9	MAX	chr10:21814409-21816690	ECC-1	luminal epithelium:	n/a	chr10:21816323-21816333 chr10:21815247-21815257 chr10:21814827-21814836
10	POLR2A	chr10:21815620-21816632	HepG2	liver:	n/a	n/a
11	POLR2A	chr10:21816220-21816603	PFSK-1	brain:	n/a	n/a
12	POLR2A	chr10:21813543-21817588	K562	blood:	n/a	n/a
13	TAF1	chr10:21816186-21816667	A549	lung:	n/a	n/a
14	TAF1	chr10:21815830-21816634	H1-hESC	embryonic stem cell:	n/a	n/a
15	POLR2A	chr10:21813587-21816614	MCF-7	breast:	n/a	n/a
16	POLR2A	chr10:21814315-21816639	U87	brain:	n/a	n/a
17	POLR2A	chr10:21814314-21816647	GM12878	blood:	n/a	n/a
18	TAF7	chr10:21813643-21816681	H1-hESC	embryonic stem cell:	n/a	n/a
19	TAF1	chr10:21815863-21816606	K562	blood:	n/a	n/a
20	MXI1	chr10:21813563-21817192	IMR90	lung:	n/a	n/a
21	POLR2A	chr10:21814229-21816637	Hela-S3	cervix:	n/a	n/a
22	HEY1	chr10:21813480-21816635	HepG2	liver:	n/a	chr10:21813521-21813536 chr10:21815495-21815510
23	POLR2A	chr10:21815097-21817178	U87	brain:	n/a	n/a
24	POLR2A	chr10:21813418-21816657	NB4	blood:	n/a	n/a
25	EP300	chr10:21816307-21818039	K562	blood:	n/a	chr10:21816401-21816410 chr10:21817917-21817931
26	BHLHE40	chr10:21813156-21816925	K562	blood:	n/a	chr10:21814887-21814903 chr10:21815069-21815085
27	IRF1	chr10:21815642-21817869	K562	blood:	n/a	chr10:21817427-21817440 chr10:21816537-21816547 chr10:21817422-21817439 chr10:21816709-21816726 chr10:21816537-21816551 chr10:21816488-21816505 chr10:21816666-21816682 chr10:21817426-21817437 chr10:21817427-21817438 chr10:21816713-21816733 chr10:21815808-21815822
28	POLR2A	chr10:21815841-21818948	H1-neurons	neurons:	n/a	n/a
29	POLR2A	chr10:21811892-21818945	H1-neurons	neurons:	n/a	n/a
30	MAX	chr10:21815941-21817050	NB4	blood:	n/a	chr10:21816323-21816333 chr10:21816880-21816888
31	POLR2A	chr10:21814333-21816596	Hela-S3	cervix:	n/a	n/a
32	GATA1	chr10:21815260-21816850	PBDE	blood:	n/a	chr10:21816578-21816585 chr10:21816578-21816585 chr10:21815754-21815764 chr10:21816578-21816589 chr10:21815299-21815309 chr10:21816573-21816589 chr10:21816578-21816585 chr10:21816571-21816592
33	POLR2A	chr10:21813549-21816618	K562	blood:	n/a	n/a
34	UBTF	chr10:21813706-21817147	K562	blood:	n/a	n/a
35	YY1	chr10:21814309-21816761	SK-N-SH	brain:	n/a	chr10:21814994-21815008 chr10:21815722-21815732 chr10:21815399-21815410 chr10:21814996-21815007 chr10:21815267-21815281 chr10:21814996-21815005 chr10:21815529-21815540 chr10:21814993-21815007 chr10:21814993-21815002 chr10:21815444-21815453 chr10:21814997-21815011 chr10:21815529-21815538 chr10:21814999-21815008
36	GATA2	chr10:21816273-21816656	HUVEC	blood vessel:	n/a	chr10:21816578-21816585 chr10:21816578-21816585 chr10:21816578-21816589 chr10:21816573-21816589 chr10:21816578-21816585 chr10:21816571-21816592
37	BCL3	chr10:21816361-21817058	A549	lung:	n/a	n/a
38	GATA3	chr10:21814277-21817147	A549	lung:	n/a	chr10:21816578-21816585 chr10:21816578-21816585 chr10:21815754-21815764 chr10:21816578-21816589 chr10:21815299-21815309 chr10:21816573-21816589 chr10:21816578-21816585 chr10:21816571-21816592
39	POLR2A	chr10:21814209-21816867	GM19099	blood:	n/a	n/a
40	MAX	chr10:21813333-21816596	HepG2	liver:	n/a	chr10:21816323-21816333 chr10:21815247-21815257 chr10:21814827-21814836 chr10:21813519-21813529
41	POLR2A	chr10:21815970-21816599	HepG2	liver:	n/a	n/a
42	MAX	chr10:21815927-21816602	H1-hESC	embryonic stem cell:	n/a	chr10:21816323-21816333
43	JUND	chr10:21816296-21817184	K562	blood:	n/a	chr10:21816868-21816877
44	MAX	chr10:21815897-21816659	SK-N-SH	brain:	n/a	chr10:21816323-21816333
45	MAX	chr10:21813003-21816989	HepG2	liver:	n/a	chr10:21816323-21816333 chr10:21815247-21815257 chr10:21816880-21816888 chr10:21814827-21814836 chr10:21813519-21813529
46	POLR2A	chr10:21813656-21817072	GM12891	blood:	n/a	n/a
47	BACH1	chr10:21816412-21817030	K562	blood:	n/a	n/a
48	POLR2A	chr10:21813582-21816675	K562	blood:	n/a	n/a
49	MAZ	chr10:21813884-21816598	HepG2	liver:	n/a	chr10:21816323-21816333 chr10:21815247-21815257 chr10:21814827-21814836
50	RCOR1	chr10:21816424-21817952	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:18946048..18948968-chr10:21815349..21817078,2	K562	blood:
2	chr10:21815110..21817816-chr10:21828150..21829882,2	MCF-7	breast:
3	chr10:21783888..21789239-chr10:21811898..21819387,16	K562	blood:
4	chr10:21480551..21484454-chr10:21814739..21816903,3	MCF-7	breast:
5	chr10:21461908..21464690-chr10:21814133..21818053,5	MCF-7	breast:
6	chr10:21774235..21777906-chr10:21814589..21817190,3	MCF-7	breast:
7	chr10:21782892..21787980-chr10:21813728..21817191,12	MCF-7	breast:
8	chr10:21814835..21816924-chr10:22010662..22012545,2	K562	blood:
9	chr10:21816369..21819253-chr10:22004806..22007546,2	MCF-7	breast:
10	chr10:21815146..21817090-chr10:22609184..22612003,2	MCF-7	breast:
11	chr10:21783009..21787738-chr10:21813105..21820576,17	MCF-7	breast:
12	chr10:21559791..21562059-chr10:21814751..21816804,2	MCF-7	breast:
13	chr10:21815035..21817998-chr10:22015362..22016989,2	MCF-7	breast:
14	chr10:21815711..21818489-chr10:22009525..22012289,2	MCF-7	breast:
15	chr10:21789609..21793052-chr10:21815401..21819121,3	MCF-7	breast:
16	chr10:21814692..21817534-chr10:22231739..22234440,2	K562	blood:
17	chr10:21815978..21818479-chr10:21973475..21976355,2	K562	blood:
18	chr10:21814767..21816695-chr10:22261629..22263190,2	MCF-7	breast:

Variant related genes	Relation type
SKIDA1	TF binding region
ENSG00000078114	Chromatin interaction
ENSG00000204682	Chromatin interaction
ENSG00000165997	Chromatin interaction
ENSG00000168283	Chromatin interaction
ENSG00000231920	Chromatin interaction
ENSG00000251749	Chromatin interaction
ENSG00000152487	Chromatin interaction
ENSG00000222071	Chromatin interaction

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10047405	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs10218956	1.00[EUR][1000 genomes]
rs11012685	1.00[TSI][hapmap]
rs11012742	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12245121	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs12245234	1.00[EUR][1000 genomes]
rs12249032	0.86[ASW][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12250810	0.88[YRI][hapmap];1.00[EUR][1000 genomes]
rs12251567	1.00[EUR][1000 genomes]
rs12251847	1.00[EUR][1000 genomes]
rs12260551	1.00[EUR][1000 genomes]
rs12266450	1.00[EUR][1000 genomes]
rs2183270	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs59876709	1.00[EUR][1000 genomes]
rs7068942	1.00[EUR][1000 genomes]
rs7076467	1.00[TSI][hapmap]
rs7083214	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs7904218	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs7910760	1.00[EUR][1000 genomes]
rs7911585	1.00[EUR][1000 genomes]
rs9971055	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv825284	chr10:21739527-21847437	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases
2	nsv825285	chr10:21742026-21874334	Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases
3	nsv825286	chr10:21757784-21838890	Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases
4	nsv825288	chr10:21759085-21831354	Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases
5	nsv825289	chr10:21762506-21845875	Strong transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases
6	nsv527055	chr10:21764019-21822856	Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases
7	nsv825290	chr10:21777857-21830878	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	33 gene(s)	inside rSNPs	diseases
8	nsv894936	chr10:21781589-21827796	Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	33 gene(s)	inside rSNPs	diseases
9	nsv550200	chr10:21782842-21824727	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	33 gene(s)	inside rSNPs	diseases
10	nsv894937	chr10:21782842-21827796	Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	33 gene(s)	inside rSNPs	diseases
11	nsv517469	chr10:21783634-21822856	Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	33 gene(s)	inside rSNPs	diseases
12	nsv894938	chr10:21784899-21827796	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	33 gene(s)	inside rSNPs	diseases
13	nsv894939	chr10:21789406-21830104	Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription 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	26 gene(s)	inside rSNPs	diseases
14	nsv825291	chr10:21792100-21830946	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
15	nsv894940	chr10:21796081-21823525	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
16	nsv550201	chr10:21796081-21824727	Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
17	nsv894941	chr10:21796081-21827796	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
18	nsv894942	chr10:21798241-21823525	Flanking Active TSS Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
19	nsv894943	chr10:21798241-21824619	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
20	nsv894944	chr10:21798241-21827796	Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
21	nsv894945	chr10:21798241-21830104	Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS 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	26 gene(s)	inside rSNPs	diseases
22	nsv894946	chr10:21798241-21831215	Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
23	nsv1052477	chr10:21810270-21889726	Active TSS Genic enhancers Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:21812400-21817400	Active TSS	Stomach Smooth Muscle	stomach
2	chr10:21812800-21818200	Active TSS	NHDF-Ad	bronchial
3	chr10:21812800-21818600	Active TSS	Right Atrium	heart
4	chr10:21813000-21816800	Active TSS	HUES6 Cell Line	embryonic stem cell
5	chr10:21813000-21816800	Active TSS	iPS-15b Cell Line	embryonic stem cell
6	chr10:21813000-21817200	Active TSS	Aorta	Aorta
7	chr10:21813000-21817400	Active TSS	Colon Smooth Muscle	Colon
8	chr10:21813000-21817400	Active TSS	Rectal Smooth Muscle	rectum
9	chr10:21813000-21818200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
10	chr10:21813000-21818200	Active TSS	Brain Anterior Caudate	brain
11	chr10:21813000-21818400	Active TSS	ES-I3 Cell Line	embryonic stem cell
12	chr10:21813000-21818400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr10:21813000-21818400	Active TSS	HSMM	muscle
14	chr10:21813000-21818600	Active TSS	H1 Cell Line	embryonic stem cell
15	chr10:21813200-21816600	Active TSS	iPS-18 Cell Line	embryonic stem cell
16	chr10:21813200-21817000	Active TSS	Fetal Stomach	stomach
17	chr10:21813200-21817400	Active TSS	Fetal Lung	lung
18	chr10:21813200-21817600	Active TSS	HUES64 Cell Line	embryonic stem cell
19	chr10:21813200-21817800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
20	chr10:21813200-21818000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr10:21813200-21818200	Active TSS	H9 Cell Line	embryonic stem cell
22	chr10:21813200-21818200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr10:21813200-21818200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr10:21813200-21818200	Active TSS	HSMMtube	muscle
25	chr10:21813200-21818400	Active TSS	Ovary	ovary
26	chr10:21813200-21818600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr10:21813200-21818800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr10:21813200-21818800	Active TSS	K562	blood
29	chr10:21813400-21816600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr10:21813400-21816800	Active TSS	HUES48 Cell Line	embryonic stem cell
31	chr10:21813400-21816800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr10:21813400-21817000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr10:21813400-21817000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr10:21813400-21817000	Active TSS	Right Ventricle	heart
35	chr10:21813400-21817000	Active TSS	Osteobl	bone
36	chr10:21813400-21817200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr10:21813400-21817200	Active TSS	Fetal Muscle Trunk	muscle
38	chr10:21813400-21817600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr10:21813400-21817600	Active TSS	Pancreatic Islets	Pancreatic Islet
40	chr10:21813400-21818000	Active TSS	iPS-20b Cell Line	embryonic stem cell
41	chr10:21813400-21818400	Active TSS	Breast Myoepithelial Primary Cells	Breast
42	chr10:21813400-21818400	Active TSS	Brain Hippocampus Middle	brain
43	chr10:21813400-21818600	Active TSS	Psoas Muscle	Psoas
44	chr10:21813400-21818600	Active TSS	A549	lung
45	chr10:21813600-21816600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr10:21813600-21816600	Active TSS	Left Ventricle	heart
47	chr10:21813600-21816600	Active TSS	Pancreas	Pancrea
48	chr10:21813600-21816800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr10:21813600-21817000	Flanking Active TSS	Primary B cells from cord blood	blood
50	chr10:21813600-21817000	Active TSS	NHLF	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links