Variant report

Variant	rs527598675
Chromosome Location	chr3:50192499-50192500
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:124)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr3:50192445-50192660	SK-N-SH	brain:	n/a	n/a
2	MAX	chr3:50192284-50192911	ECC-1	luminal epithelium:	n/a	n/a
3	REST	chr3:50191706-50193577	H1-neurons	neurons:	n/a	chr3:50192632-50192645 chr3:50193092-50193102 chr3:50192628-50192648 chr3:50193114-50193124 chr3:50192001-50192014 chr3:50192628-50192648
4	TAF1	chr3:50192415-50192703	Hela-S3	cervix:	n/a	n/a
5	CREB1	chr3:50192309-50193270	HepG2	liver:	n/a	n/a
6	POLR2A	chr3:50192415-50192716	Hela-S3	cervix:	n/a	n/a
7	YY1	chr3:50192320-50192651	K562	blood:	n/a	chr3:50192468-50192482 chr3:50192612-50192626
8	POLR2A	chr3:50192417-50192800	A549	lung:	n/a	n/a
9	CHD2	chr3:50192367-50192705	K562	blood:	n/a	n/a
10	POLR2A	chr3:50191801-50192942	MCF-7	breast:	n/a	n/a
11	POLR2A	chr3:50192418-50192696	HepG2	liver:	n/a	n/a
12	MYC	chr3:50192438-50192650	MCF10A-Er-Src	breast:	n/a	n/a
13	TAF1	chr3:50192168-50192786	ECC-1	luminal epithelium:	n/a	n/a
14	POLR2A	chr3:50192408-50192765	H1-hESC	embryonic stem cell:	n/a	n/a
15	GABPA	chr3:50192430-50193104	H1-hESC	embryonic stem cell:	n/a	chr3:50192889-50192898
16	SIN3AK20	chr3:50192385-50193019	PANC-1	pancreas:	n/a	n/a
17	TAF1	chr3:50192374-50192758	HepG2	liver:	n/a	n/a
18	TBP	chr3:50192431-50192650	K562	blood:	n/a	n/a
19	RAD21	chr3:50192458-50192910	HepG2	liver:	n/a	chr3:50192717-50192727
20	GABPA	chr3:50192484-50193046	H1-hESC	embryonic stem cell:	n/a	chr3:50192889-50192898
21	EGR1	chr3:50192108-50192602	MCF-7	breast:	n/a	chr3:50192268-50192282
22	HEY1	chr3:50192284-50192786	HepG2	liver:	n/a	chr3:50192605-50192620 chr3:50192671-50192686
23	CEBPD	chr3:50192386-50192681	HepG2	liver:	n/a	n/a
24	RAD21	chr3:50192496-50192894	IMR90	lung:	n/a	chr3:50192717-50192727
25	CHD1	chr3:50192283-50194228	IMR90	lung:	n/a	n/a
26	POLR2A	chr3:50191962-50192809	H1-neurons	neurons:	n/a	n/a
27	MAZ	chr3:50192468-50192846	Hela-S3	cervix:	n/a	n/a
28	POLR2A	chr3:50192428-50192692	A549	lung:	n/a	n/a
29	RAD21	chr3:50192447-50192984	ECC-1	luminal epithelium:	n/a	chr3:50192717-50192727
30	UBTF	chr3:50192398-50193168	K562	blood:	n/a	n/a
31	MAX	chr3:50192379-50192839	K562	blood:	n/a	n/a
32	POLR2A	chr3:50192362-50192958	HepG2	liver:	n/a	n/a
33	POLR2A	chr3:50192392-50192665	H1-hESC	embryonic stem cell:	n/a	n/a
34	HEY1	chr3:50192469-50192744	K562	blood:	n/a	chr3:50192605-50192620 chr3:50192671-50192686
35	POLR2A	chr3:50192389-50192693	K562	blood:	n/a	n/a
36	POLR2A	chr3:50192275-50192681	ECC-1	luminal epithelium:	n/a	n/a
37	CCNT2	chr3:50192446-50193005	K562	blood:	n/a	n/a
38	POLR2A	chr3:50192125-50192837	MCF-7	breast:	n/a	n/a
39	POLR2A	chr3:50192387-50192811	IMR90	lung:	n/a	n/a
40	POLR2A	chr3:50192422-50192703	HepG2	liver:	n/a	n/a
41	POLR2A	chr3:50192387-50192691	Hela-S3	cervix:	n/a	n/a
42	RAD21	chr3:50192405-50192978	HepG2	liver:	n/a	chr3:50192717-50192727
43	POLR2A	chr3:50192437-50192670	HepG2	liver:	n/a	n/a
44	POLR2A	chr3:50192131-50192922	MCF-7	breast:	n/a	n/a
45	PAX5	chr3:50192470-50192812	GM12892	blood:	n/a	chr3:50192608-50192617
46	POLR2A	chr3:50192356-50192725	SK-N-SH	brain:	n/a	n/a
47	POLR2A	chr3:50191934-50192829	H1-neurons	neurons:	n/a	n/a
48	SMARCB1	chr3:50192068-50193631	Hela-S3	cervix:	n/a	n/a
49	POLR2A	chr3:50192429-50192687	A549	lung:	n/a	n/a
50	POLR2A	chr3:50192203-50192912	HUVEC	blood vessel:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:50192449-50192499	NHDF-neo	bronchial:	n/a
2	chr3:50192449-50192499	PFSK-1	brain:	n/a
3	chr3:50192449-50192499	MCF-7	breast:	n/a
4	chr3:50192449-50192499	HEEpiC	esophagus:	n/a
5	chr3:50192449-50192499	LNCaP	prostate:	n/a
6	chr3:50192449-50192499	HAEpiC	amniotic membrane:	n/a
7	chr3:50192449-50192499	H1-hESC	embryonic stem cell:	embryo
8	chr3:50192449-50192499	NHBE	bronchial:	n/a
9	chr3:50192449-50192499	AG04450	lung:	fetal
10	chr3:50192449-50192499	HRPEpiC	eye:	n/a
11	chr3:50192449-50192499	AoSMC	blood vessel:	n/a
12	chr3:50192449-50192499	HepG2	liver:	n/a
13	chr3:50192449-50192499	ECC-1	luminal epithelium:	n/a
14	chr3:50192449-50192499	BE2_C	brain:	n/a
15	chr3:50192449-50192499	HMEC	breast:	n/a
16	chr3:50192449-50192499	HRE	kidney:	n/a
17	chr3:50192449-50192499	Jurkat	blood:	n/a
18	chr3:50192449-50192499	AG10803	skin:	n/a
19	chr3:50192449-50192499	SAEC	small airway:	n/a
20	chr3:50192449-50192499	PANC-1	pancreas:	n/a
21	chr3:50192449-50192499	HCF	heart:	n/a
22	chr3:50192449-50192499	T-47D	breast:	n/a
23	chr3:50192449-50192499	SK-N-SH	brain:	n/a
24	chr3:50192449-50192499	PrEC	prostate:	n/a
25	chr3:50192449-50192499	GM19239	blood:	n/a
26	chr3:50192449-50192499	AG09319	gingival:	n/a
27	chr3:50192449-50192499	GM12892	blood:	n/a
28	chr3:50192449-50192499	SK-N-MC	brain:	n/a
29	chr3:50192449-50192499	HEK293	kidney:	embryo
30	chr3:50192449-50192499	HPAEpiC	pulmonary alveolar:	n/a
31	chr3:50192449-50192499	BJ	skin:	n/a
32	chr3:50192449-50192499	A549	lung:	n/a
33	chr3:50192449-50192499	MCF10A-Er-Src	breast:	n/a
34	chr3:50192449-50192499	HNPCEpiC	eye:	n/a
35	chr3:50192449-50192499	HCPEpiC	choroid plexus:	n/a
36	chr3:50192449-50192499	HCM	heart:	n/a
37	chr3:50192449-50192499	HRCEpiC	kidney:	n/a
38	chr3:50192449-50192499	RPTEC	kidney:	n/a
39	chr3:50192449-50192499	SK-N-SH_RA	brain:	n/a
40	chr3:50192449-50192499	GM12891	blood:	n/a
41	chr3:50192449-50192499	HUVEC	blood vessel:	n/a
42	chr3:50192449-50192499	HL-60	blood:	n/a
43	chr3:50192449-50192499	HCT-116	colon:	n/a
44	chr3:50192449-50192499	Caco-2	colon:	n/a
45	chr3:50192449-50192499	IMR90	lung:	fetal
46	chr3:50192449-50192499	NT2-D1	testis:	n/a
47	chr3:50192449-50192499	K562	blood:	n/a
48	chr3:50192449-50192499	NB4	blood:	n/a
49	chr3:50192449-50192499	GM12878	blood:	n/a
50	chr3:50192449-50192499	CMK	blood:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:50191641..50194297-chr3:50220054..50223610,4	MCF-7	breast:
2	chr3:50190470..50194491-chr3:50196225..50201802,7	K562	blood:
3	chr3:50191627..50193691-chr3:50209687..50211278,2	MCF-7	breast:
4	chr3:50191338..50193199-chr3:50263040..50265048,2	MCF-7	breast:
5	chr3:50191401..50200098-chr3:50206213..50213809,14	MCF-7	breast:

No data

Variant related genes	Relation type
SEMA3F	TF binding region
SEMA3F	CpG island
ENSG00000207922	Chromatin interaction
ENSG00000114353	Chromatin interaction
ENSG00000001617	Chromatin interaction

Extended variants
information (count: 26 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:26 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834690	chr3:50101835-50267584	Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv515986	chr3:50104307-50267584	Bivalent Enhancer Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv432418	chr3:50114496-50224196	Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
4	nsv1001775	chr3:50129479-50311666	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
5	nsv876768	chr3:50144951-50267584	Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
6	nsv523662	chr3:50144951-50584999	Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	101 gene(s)	inside rSNPs	diseases
7	nsv1013949	chr3:50151712-50339163	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
8	nsv590250	chr3:50153356-50332697	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active 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	43 gene(s)	inside rSNPs	diseases
9	nsv876769	chr3:50155468-50408398	Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
10	esv1821728	chr3:50156142-50657253	Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
11	esv1793751	chr3:50157364-50476363	Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
12	esv1828162	chr3:50157364-50506151	Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
13	nsv590251	chr3:50158774-50337422	Active TSS Strong transcription Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer 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 miRNA target site	53 gene(s)	inside rSNPs	diseases
14	nsv470561	chr3:50158774-50584999	Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	99 gene(s)	inside rSNPs	diseases
15	nsv876770	chr3:50158774-50609624	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
16	nsv523560	chr3:50172397-50339163	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer 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 miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
17	nsv460529	chr3:50178011-50324672	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
18	nsv460530	chr3:50178011-50324672	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
19	nsv590252	chr3:50178011-50324672	Enhancers Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Genic enhancers 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	40 gene(s)	inside rSNPs	diseases
20	nsv1002916	chr3:50187646-50311666	Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
21	nsv536564	chr3:50187646-50311666	Flanking Active TSS Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
22	nsv1014256	chr3:50187646-50339163	Enhancers Active TSS Strong transcription Weak transcription Genic enhancers Bivalent/Poised TSS Flanking 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 miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
23	nsv536565	chr3:50187646-50339163	Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
24	nsv1001993	chr3:50187646-50640808	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
25	esv3323037	chr3:50190548-50194846	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
26	esv3356010	chr3:50191398-50194246	Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:103 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:50189600-50193000	Weak transcription	Fetal Lung	lung
2	chr3:50190000-50193000	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr3:50191600-50193200	Bivalent/Poised TSS	Primary T cells from cord blood	blood
4	chr3:50191600-50193400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
5	chr3:50191800-50192600	Enhancers	Liver	Liver
6	chr3:50191800-50193000	Active TSS	Brain Anterior Caudate	brain
7	chr3:50191800-50193200	Active TSS	Rectal Smooth Muscle	rectum
8	chr3:50191800-50193400	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr3:50191800-50193400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
10	chr3:50191800-50193400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr3:50191800-50193400	Active TSS	Fetal Brain Female	brain
12	chr3:50191800-50193400	Active TSS	Hela-S3	cervix
13	chr3:50191800-50194400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr3:50192000-50192600	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr3:50192000-50192600	Weak transcription	Fetal Kidney	kidney
16	chr3:50192000-50193000	Active TSS	HUES48 Cell Line	embryonic stem cell
17	chr3:50192000-50193000	Active TSS	Primary T helper naive cells fromperipheralblood	blood
18	chr3:50192000-50193000	Weak transcription	Fetal Heart	heart
19	chr3:50192000-50193000	Active TSS	HSMMtube	muscle
20	chr3:50192000-50193200	Bivalent/Poised TSS	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr3:50192000-50193200	Active TSS	iPS-15b Cell Line	embryonic stem cell
22	chr3:50192000-50193200	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
23	chr3:50192000-50193200	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
24	chr3:50192000-50193200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
25	chr3:50192000-50193200	Weak transcription	Fetal Brain Male	brain
26	chr3:50192000-50193200	Active TSS	Rectal Mucosa Donor 31	rectum
27	chr3:50192000-50193200	Active TSS	A549	lung
28	chr3:50192000-50193200	Bivalent/Poised TSS	HSMM	muscle
29	chr3:50192000-50193400	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
30	chr3:50192000-50193400	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr3:50192000-50193400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
32	chr3:50192000-50193400	Active TSS	K562	blood
33	chr3:50192000-50193600	Active TSS	Aorta	Aorta
34	chr3:50192000-50193600	Active TSS	Small Intestine	intestine
35	chr3:50192000-50193800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
36	chr3:50192000-50194400	Active TSS	Pancreatic Islets	Pancreatic Islet
37	chr3:50192000-50194400	Active TSS	Psoas Muscle	Psoas
38	chr3:50192000-50194800	Active TSS	H9 Cell Line	embryonic stem cell
39	chr3:50192000-50194800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr3:50192000-50194800	Active TSS	Gastric	stomach
41	chr3:50192000-50194800	Active TSS	Left Ventricle	heart
42	chr3:50192000-50194800	Active TSS	Right Atrium	heart
43	chr3:50192200-50192600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr3:50192200-50192600	Active TSS	Primary hematopoietic stem cells	blood
45	chr3:50192200-50192600	Active TSS	Primary T helper naive cells from peripheral blood	blood
46	chr3:50192200-50192600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
47	chr3:50192200-50192600	Bivalent/Poised TSS	Thymus	Thymus
48	chr3:50192200-50192800	Bivalent/Poised TSS	Primary neutrophils fromperipheralblood	blood
49	chr3:50192200-50192800	Bivalent/Poised TSS	Primary T regulatory cells fromperipheralblood	blood
50	chr3:50192200-50192800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links