Variant report

Variant	rs576449813
Chromosome Location	chr12:568981-568982
allele	A/G
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	MAX	chr12:568548-569008	H1-hESC	embryonic stem cell:	n/a	chr12:568932-568942
2	E2F6	chr12:568487-569024	H1-hESC	embryonic stem cell:	n/a	n/a
3	MAX	chr12:568493-569442	ECC-1	luminal epithelium:	n/a	chr12:568932-568942
4	MAX	chr12:568503-568997	A549	lung:	n/a	chr12:568932-568942
5	EGR1	chr12:568558-569445	ECC-1	luminal epithelium:	n/a	chr12:569343-569352 chr12:568929-568942
6	CHD2	chr12:568587-568985	H1-hESC	embryonic stem cell:	n/a	n/a
7	SIN3A	chr12:568822-569377	H1-hESC	embryonic stem cell:	n/a	chr12:569335-569346
8	MAX	chr12:568343-569415	HCT-116	colon:	n/a	chr12:568932-568942
9	CTCF	chr12:568840-568990	HepG2	liver:	n/a	n/a
10	POLR2A	chr12:568715-569350	HCT-116	colon:	n/a	n/a
11	CREB1	chr12:568572-569088	H1-hESC	embryonic stem cell:	n/a	n/a
12	E2F6	chr12:568465-569081	A549	lung:	n/a	n/a
13	POLR2A	chr12:568736-569436	PFSK-1	brain:	n/a	n/a
14	EGR1	chr12:568614-569455	HCT-116	colon:	n/a	chr12:569343-569352 chr12:568929-568942
15	POLR2A	chr12:568887-569677	HEK293	kidney:	n/a	n/a
16	MAX	chr12:568464-570097	ECC-1	luminal epithelium:	n/a	chr12:569928-569938 chr12:569929-569939 chr12:569928-569939 chr12:569928-569939 chr12:569929-569938 chr12:569870-569880 chr12:569929-569938 chr12:568932-568942 chr12:569929-569938
17	EGR1	chr12:568837-569452	ECC-1	luminal epithelium:	n/a	chr12:569343-569352 chr12:568929-568942
18	POLR2A	chr12:568958-569399	H1-hESC	embryonic stem cell:	n/a	n/a
19	SETDB1	chr12:568187-568986	U2OS	brain:	n/a	n/a
20	ZBTB7A	chr12:568555-570184	ECC-1	luminal epithelium:	n/a	chr12:568929-568938
21	E2F6	chr12:568342-569224	H1-hESC	embryonic stem cell:	n/a	n/a
22	POLR2A	chr12:568769-569046	ECC-1	luminal epithelium:	n/a	n/a
23	MAX	chr12:568436-569478	A549	lung:	n/a	chr12:568932-568942
24	TCF12	chr12:568455-570024	ECC-1	luminal epithelium:	n/a	n/a
25	MAX	chr12:568504-569469	H1-hESC	embryonic stem cell:	n/a	chr12:568932-568942
26	EGR1	chr12:568859-569302	K562	blood:	n/a	chr12:568929-568942
27	KAP1	chr12:568243-568989	U2OS	brain:	n/a	n/a
28	ZBTB7A	chr12:568666-570181	ECC-1	luminal epithelium:	n/a	chr12:568929-568938
29	CREB1	chr12:568611-569201	H1-hESC	embryonic stem cell:	n/a	n/a
30	POLR2A	chr12:568804-569398	HCT-116	colon:	n/a	n/a
31	YY1	chr12:568901-569057	HCT-116	colon:	n/a	n/a
32	TAF1	chr12:568689-569477	ECC-1	luminal epithelium:	n/a	n/a
33	GATA3	chr12:568139-568993	MCF-7	breast:	n/a	chr12:568182-568195 chr12:568476-568484
34	EGR1	chr12:568901-569305	K562	blood:	n/a	chr12:568929-568942

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:568931-568981	NHDF-neo	bronchial:	n/a
2	chr12:568931-568981	Hepatocyte	liver:	n/a
3	chr12:568931-568981	SAEC	small airway:	n/a
4	chr12:568931-568981	HEEpiC	esophagus:	n/a
5	chr12:568931-568981	SK-N-SH	brain:	n/a
6	chr12:568931-568981	Hela-S3	cervix:	n/a
7	chr12:568931-568981	HepG2	liver:	n/a
8	chr12:568931-568981	AoSMC	blood vessel:	n/a
9	chr12:568931-568981	T-47D	breast:	n/a
10	chr12:568931-568981	HMEC	breast:	n/a
11	chr12:568931-568981	HCF	heart:	n/a
12	chr12:568931-568981	AG09319	gingival:	n/a
13	chr12:568931-568981	GM12892	blood:	n/a
14	chr12:568931-568981	HRE	kidney:	n/a
15	chr12:568931-568981	HPAEpiC	pulmonary alveolar:	n/a
16	chr12:568931-568981	SK-N-SH_RA	brain:	n/a
17	chr12:568931-568981	MCF10A-Er-Src	breast:	n/a
18	chr12:568931-568981	NHBE	bronchial:	n/a
19	chr12:568931-568981	GM12878	blood:	n/a
20	chr12:568931-568981	Caco-2	colon:	n/a
21	chr12:568931-568981	AG04450	lung:	fetal
22	chr12:568931-568981	HCM	heart:	n/a
23	chr12:568931-568981	PrEC	prostate:	n/a
24	chr12:568931-568981	HUVEC	blood vessel:	n/a
25	chr12:568931-568981	HRCEpiC	kidney:	n/a
26	chr12:568931-568981	SKMC	muscle:	n/a
27	chr12:568931-568981	AG10803	skin:	n/a
28	chr12:568931-568981	ECC-1	luminal epithelium:	n/a
29	chr12:568931-568981	SK-N-MC	brain:	n/a
30	chr12:568931-568981	PFSK-1	brain:	n/a
31	chr12:568931-568981	AG04449	skin:	fetal
32	chr12:568931-568981	U87	brain:	n/a
33	chr12:568931-568981	HNPCEpiC	eye:	n/a
34	chr12:568931-568981	NT2-D1	testis:	n/a
35	chr12:568931-568981	GM19239	blood:	n/a
36	chr12:568931-568981	Jurkat	blood:	n/a
37	chr12:568931-568981	MCF-7	breast:	n/a
38	chr12:568931-568981	K562	blood:	n/a
39	chr12:568931-568981	GM06990	blood:	n/a
40	chr12:568931-568981	BJ	skin:	n/a
41	chr12:568931-568981	HCPEpiC	choroid plexus:	n/a
42	chr12:568931-568981	ovcar-3	ovarian:	n/a
43	chr12:568931-568981	HAEpiC	amniotic membrane:	n/a
44	chr12:568931-568981	HRPEpiC	eye:	n/a
45	chr12:568931-568981	RPTEC	kidney:	n/a
46	chr12:568931-568981	H1-hESC	embryonic stem cell:	embryo
47	chr12:568931-568981	HIPEpiC	eye:	n/a
48	chr12:568931-568981	CMK	blood:	n/a
49	chr12:568931-568981	A549	lung:	n/a
50	chr12:568931-568981	GM12891	blood:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:563329..565508-chr12:567009..569483,2	MCF-7	breast:

Variant related genes	Relation type
B4GALNT3	TF binding region
B4GALNT3	CpG island

Extended variants
information (count: 33 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:33 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv541304	chr12:282465-635505	Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
2	nsv1042991	chr12:282465-666255	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	nsv1041574	chr12:282465-812000	Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
4	nsv541305	chr12:282465-1016828	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
5	nsv869390	chr12:282465-1045994	Strong transcription Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
6	nsv1049944	chr12:282465-1232077	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer 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 miRNA target site	80 gene(s)	inside rSNPs	diseases
7	nsv541306	chr12:282465-1232077	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
8	nsv1050781	chr12:321353-783899	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
9	nsv1040849	chr12:321619-771493	Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
10	nsv541322	chr12:321619-771493	ZNF genes & repeats Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
11	nsv1035679	chr12:321619-781558	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
12	nsv1053519	chr12:321619-828175	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
13	nsv1044433	chr12:321619-1065402	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
14	nsv541323	chr12:321619-1065402	Strong transcription Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
15	esv2759875	chr12:335010-990544	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
16	nsv1045638	chr12:349031-893536	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
17	nsv541325	chr12:349031-893536	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	48 gene(s)	inside rSNPs	diseases
18	nsv1050646	chr12:362398-658665	Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
19	nsv541326	chr12:362398-658665	Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
20	nsv949469	chr12:380411-1122450	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
21	nsv1050226	chr12:441032-743195	Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
22	esv2758290	chr12:457433-990544	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
23	nsv949226	chr12:493900-814882	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
24	nsv898566	chr12:499041-570917	Flanking Bivalent TSS/Enh Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
25	nsv1036822	chr12:504573-586674	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
26	nsv541329	chr12:504573-586674	Strong transcription Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
27	nsv1048923	chr12:527728-658665	Weak transcription Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
28	nsv541330	chr12:527728-658665	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
29	nsv898567	chr12:547683-863517	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
30	nsv898568	chr12:547683-969800	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
31	nsv430441	chr12:551550-628236	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
32	nsv1046514	chr12:554091-633417	Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
33	esv3447018	chr12:568191-570739	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 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	chr12:568200-569000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
2	chr12:568400-569000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
3	chr12:568400-569000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
4	chr12:568400-569000	Flanking Bivalent TSS/Enh	Primary T cells from cord blood	blood
5	chr12:568400-569000	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
6	chr12:568400-569000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
7	chr12:568400-569000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
8	chr12:568400-569000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
9	chr12:568400-569000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
10	chr12:568400-569000	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
11	chr12:568400-569000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr12:568400-569000	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
13	chr12:568400-569000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
14	chr12:568400-569000	Flanking Bivalent TSS/Enh	Rectal Smooth Muscle	rectum
15	chr12:568400-569000	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
16	chr12:568400-569000	Flanking Bivalent TSS/Enh	HepG2	liver
17	chr12:568400-569000	Flanking Active TSS	NHEK	skin
18	chr12:568400-570200	Bivalent/Poised TSS	A549	lung
19	chr12:568400-570400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
20	chr12:568400-570400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
21	chr12:568400-570600	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr12:568400-570800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
23	chr12:568400-570800	Bivalent/Poised TSS	Fetal Brain Female	brain
24	chr12:568400-570800	Active TSS	Right Atrium	heart
25	chr12:568400-571200	Active TSS	Pancreatic Islets	Pancreatic Islet
26	chr12:568600-569000	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr12:568600-569000	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr12:568600-569000	Flanking Bivalent TSS/Enh	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr12:568600-569000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr12:568600-569000	Flanking Bivalent TSS/Enh	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr12:568600-569000	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr12:568600-569000	Flanking Bivalent TSS/Enh	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr12:568600-569000	Flanking Bivalent TSS/Enh	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr12:568600-569000	Flanking Bivalent TSS/Enh	Primary neutrophils fromperipheralblood	blood
35	chr12:568600-569000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells	blood
36	chr12:568600-569000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
37	chr12:568600-569000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
38	chr12:568600-569000	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr12:568600-569000	Flanking Bivalent TSS/Enh	Primary Natural Killer cells fromperipheralblood	blood
40	chr12:568600-569000	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
41	chr12:568600-569000	Active TSS	Primary T killer memory cells from peripheral blood	blood
42	chr12:568600-569000	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr12:568600-569000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr12:568600-569000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr12:568600-569000	Flanking Bivalent TSS/Enh	Muscle Satellite Cultured Cells	--
46	chr12:568600-569000	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
47	chr12:568600-569000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr12:568600-569000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr12:568600-569000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr12:568600-569000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin

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