Variant report

Variant	rs2861485
Chromosome Location	chr19:35738400-35738401
allele	A/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	RUNX3	chr19:35738364-35740434	GM12878	blood:	n/a	n/a
2	ELF1	chr19:35738391-35740209	MCF-7	breast:	n/a	chr19:35739566-35739575 chr19:35739565-35739576 chr19:35739565-35739576
3	SP1	chr19:35738363-35740122	H1-hESC	embryonic stem cell:	n/a	chr19:35739574-35739588 chr19:35739591-35739600 chr19:35739125-35739139 chr19:35738973-35738980
4	RFX5	chr19:35738388-35740137	Hela-S3	cervix:	n/a	n/a
5	CBX3	chr19:35738277-35738891	K562	blood:	n/a	n/a
6	SIN3AK20	chr19:35738395-35740428	MCF-7	breast:	n/a	n/a
7	POLR2A	chr19:35738277-35740787	HCT-116	colon:	n/a	n/a
8	HCFC1	chr19:35738387-35740287	K562	blood:	n/a	n/a
9	CTCF	chr19:35738400-35738550	GM12866	blood:	n/a	n/a
10	JUND	chr19:35738299-35740409	HCT-116	colon:	n/a	chr19:35740274-35740288
11	EGR1	chr19:35738254-35740279	HCT-116	colon:	n/a	chr19:35740248-35740257 chr19:35739206-35739216 chr19:35739470-35739494 chr19:35738608-35738622 chr19:35740103-35740113 chr19:35739565-35739574
12	MAX	chr19:35738343-35740284	K562	blood:	n/a	chr19:35739208-35739218 chr19:35740104-35740114
13	SIN3AK20	chr19:35738396-35739022	K562	blood:	n/a	n/a
14	RAD21	chr19:35738363-35739463	H1-hESC	embryonic stem cell:	n/a	chr19:35738834-35738847 chr19:35738831-35738850 chr19:35738775-35738784 chr19:35738833-35738845 chr19:35738835-35738845
15	POLR2A	chr19:35738305-35740223	HCT-116	colon:	n/a	n/a
16	TAF7	chr19:35738312-35740211	H1-hESC	embryonic stem cell:	n/a	n/a
17	MYC	chr19:35738277-35740509	K562	blood:	n/a	chr19:35739208-35739218 chr19:35740104-35740114
18	BHLHE40	chr19:35738376-35740338	GM12878	blood:	n/a	n/a
19	GABPA	chr19:35738360-35740176	MCF-7	breast:	n/a	chr19:35738936-35738943
20	EP300	chr19:35738343-35740111	H1-hESC	embryonic stem cell:	n/a	chr19:35739338-35739354 chr19:35739566-35739573
21	RAD21	chr19:35738395-35739086	MCF-7	breast:	n/a	chr19:35738834-35738847 chr19:35738831-35738850 chr19:35738775-35738784 chr19:35738833-35738845 chr19:35738835-35738845
22	YY1	chr19:35738393-35738630	K562	blood:	n/a	n/a
23	YY1	chr19:35738297-35738992	H1-hESC	embryonic stem cell:	n/a	n/a
24	HDAC2	chr19:35738369-35739137	K562	blood:	n/a	n/a
25	TBP	chr19:35738388-35740314	K562	blood:	n/a	n/a
26	STAT3	chr19:35738314-35739836	MCF10A-Er-Src	breast:	n/a	chr19:35738922-35738930 chr19:35738920-35738931 chr19:35738922-35738931 chr19:35738916-35738936 chr19:35738921-35738930
27	POLR2A	chr19:35738323-35740466	GM12878	blood:	n/a	n/a
28	MAX	chr19:35738322-35739810	A549	lung:	n/a	chr19:35739208-35739218
29	RAD21	chr19:35738324-35739045	HepG2	liver:	n/a	chr19:35738834-35738847 chr19:35738831-35738850 chr19:35738775-35738784 chr19:35738833-35738845 chr19:35738835-35738845
30	IRF4	chr19:35738354-35738935	GM12878	blood:	n/a	chr19:35738744-35738758
31	YY1	chr19:35738393-35740164	GM12878	blood:	n/a	chr19:35739906-35739926
32	CREB1	chr19:35738364-35740231	H1-hESC	embryonic stem cell:	n/a	n/a
33	STAT5A	chr19:35738339-35739041	K562	blood:	n/a	chr19:35738922-35738930 chr19:35738922-35738931 chr19:35738916-35738936 chr19:35738921-35738930
34	SP1	chr19:35737993-35740296	HCT-116	colon:	n/a	chr19:35739574-35739588 chr19:35739591-35739600 chr19:35739125-35739139 chr19:35738973-35738980
35	CBX3	chr19:35738120-35739047	K562	blood:	n/a	n/a
36	ATF2	chr19:35738361-35739041	H1-hESC	embryonic stem cell:	n/a	n/a
37	MYBL2	chr19:35738392-35740284	HepG2	liver:	n/a	n/a
38	TCF12	chr19:35738345-35740313	ECC-1	luminal epithelium:	n/a	n/a
39	MAX	chr19:35738261-35740221	ECC-1	luminal epithelium:	n/a	chr19:35739208-35739218 chr19:35740104-35740114
40	MAX	chr19:35738204-35740314	HCT-116	colon:	n/a	chr19:35739208-35739218 chr19:35740104-35740114
41	USF2	chr19:35738393-35739127	H1-hESC	embryonic stem cell:	n/a	n/a
42	ARID3A	chr19:35738377-35738936	K562	blood:	n/a	n/a
43	POLR2A	chr19:35738370-35740307	K562	blood:	n/a	n/a
44	USF1	chr19:35738259-35738941	H1-hESC	embryonic stem cell:	n/a	n/a
45	KAP1	chr19:35737433-35739008	K562	blood:	n/a	n/a
46	HDAC2	chr19:35738391-35738929	K562	blood:	n/a	n/a
47	POLR2A	chr19:35738375-35741593	H1-hESC	embryonic stem cell:	n/a	n/a
48	POLR2A	chr19:35738380-35740286	GM12892	blood:	n/a	n/a
49	MAX	chr19:35738391-35740367	HepG2	liver:	n/a	chr19:35739208-35739218 chr19:35740104-35740114
50	SP1	chr19:35738395-35740089	H1-hESC	embryonic stem cell:	n/a	chr19:35739574-35739588 chr19:35739591-35739600 chr19:35739125-35739139 chr19:35738973-35738980

No.	Distal block	Cell Line	Cell type
1	chr19:35654052..35658593-chr19:35736953..35742683,9	K562	blood:
2	chr19:35639021..35648956-chr19:35737438..35742195,14	K562	blood:
3	chr19:35604580..35611543-chr19:35737733..35741283,12	MCF-7	breast:
4	chr19:35738397..35739313-chr19:35760217..35761209,4	K562	blood:
5	chr19:35625494..35628326-chr19:35738306..35742693,4	MCF-7	breast:
6	chr19:35723373..35727135-chr19:35736732..35741150,5	MCF-7	breast:
7	chr19:35728933..35734246-chr19:35734922..35738680,5	K562	blood:
8	chr19:35531384..35534577-chr19:35737191..35741282,3	MCF-7	breast:
9	chr19:35519110..35522906-chr19:35737918..35741487,5	MCF-7	breast:
10	chr19:35490465..35492383-chr19:35737631..35740321,3	MCF-7	breast:
11	chr19:35644753..35650464-chr19:35737058..35742117,12	K562	blood:
12	chr19:35734847..35736639-chr19:35736785..35738777,2	MCF-7	breast:
13	chr19:35603872..35607710-chr19:35737437..35742074,6	MCF-7	breast:
14	chr19:35625357..35628180-chr19:35737479..35741018,4	MCF-7	breast:
15	chr19:35633841..35634348-chr19:35738374..35738913,2	MCF-7	breast:
16	chr19:35631922..35638346-chr19:35737284..35742337,12	MCF-7	breast:
17	chr19:35719165..35720695-chr19:35737226..35739057,2	MCF-7	breast:
18	chr19:35630586..35637861-chr19:35737374..35742554,18	MCF-7	breast:
19	chr19:35714125..35716071-chr19:35737131..35738946,2	MCF-7	breast:

Variant related genes	Relation type
LSR	TF binding region
ENSG00000089356	Chromatin interaction
ENSG00000266964	Chromatin interaction
ENSG00000105698	Chromatin interaction
ENSG00000221946	Chromatin interaction
ENSG00000153902	Chromatin interaction
ENSG00000269303	Chromatin interaction
ENSG00000105707	Chromatin interaction
ENSG00000262497	Chromatin interaction
ENSG00000177558	Chromatin interaction
ENSG00000105711	Chromatin interaction
ENSG00000089351	Chromatin interaction
ENSG00000089327	Chromatin interaction

Extended variants
information (count: 50 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10407740	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10411872	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10412357	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10416254	0.96[CEU][hapmap];0.87[YRI][hapmap];0.87[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs10418562	0.96[CEU][hapmap];0.91[YRI][hapmap];0.87[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs10421791	0.93[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10422195	0.96[CEU][hapmap];0.90[LWK][hapmap];0.83[MEX][hapmap];0.95[MKK][hapmap];1.00[TSI][hapmap];0.87[YRI][hapmap];0.87[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs10424110	0.87[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs11084809	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.91[YRI][hapmap];0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11669258	0.96[CEU][hapmap];0.90[LWK][hapmap];0.83[MEX][hapmap];0.95[MKK][hapmap];1.00[TSI][hapmap];0.87[YRI][hapmap];0.87[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs12609790	0.94[CEU][hapmap];0.89[YRI][hapmap];0.87[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs12742	0.82[ASN][1000 genomes]
rs1882694	0.90[CHB][hapmap];0.97[CHD][hapmap];0.94[JPT][hapmap]
rs2073900	0.80[YRI][hapmap]
rs2188327	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2861487	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2861488	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs34926220	0.88[AFR][1000 genomes];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4805118	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4806115	0.90[GIH][hapmap]
rs4806117	0.96[CEU][hapmap];0.87[YRI][hapmap];0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4806119	0.86[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4806122	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4806123	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56209605	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6510474	0.88[AFR][1000 genomes];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7248460	0.96[CEU][hapmap];0.87[YRI][hapmap];0.85[AFR][1000 genomes];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7249852	0.88[AFR][1000 genomes];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7249941	0.88[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs7249962	0.88[AFR][1000 genomes];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7250531	0.87[AFR][1000 genomes];0.94[EUR][1000 genomes]
rs7251826	0.85[ASW][hapmap];0.87[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.91[MKK][hapmap];1.00[TSI][hapmap];0.95[YRI][hapmap];0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7253876	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7255786	0.83[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs7256604	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73029964	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73029965	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73029970	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7359971	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8112032	0.96[CEU][hapmap];0.90[LWK][hapmap];0.83[MEX][hapmap];0.95[MKK][hapmap];1.00[TSI][hapmap];0.87[YRI][hapmap];0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432045	chr19:35556260-36520760	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS 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	191 gene(s)	inside rSNPs	diseases
2	nsv1060100	chr19:35658505-36170042	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
3	nsv543993	chr19:35658505-36170042	Enhancers Strong transcription Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh 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	107 gene(s)	inside rSNPs	diseases
4	nsv1066553	chr19:35698638-35749563	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
5	esv2763203	chr19:35700047-35738400	Flanking Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
6	nsv510765	chr19:35708226-35890668	Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
7	esv2758497	chr19:35711078-35887113	Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
8	esv2758758	chr19:35711078-35887113	Bivalent Enhancer Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
9	nsv978896	chr19:35724047-35748472	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
10	nsv911618	chr19:35734107-35807845	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs2861485	CD177	cis	parietal	SCAN
rs2861485	ZNF383	cis	parietal	SCAN
rs2861485	FCGBP	cis	cerebellum	SCAN

Chromatin state (count:102 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:35737400-35739000	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
2	chr19:35737600-35738400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr19:35737600-35738400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr19:35737600-35738400	Enhancers	Adipose Nuclei	Adipose
5	chr19:35737600-35738400	Enhancers	Hela-S3	cervix
6	chr19:35737600-35740600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
7	chr19:35737800-35738400	Enhancers	Stomach Mucosa	stomach
8	chr19:35737800-35738400	Enhancers	HMEC	breast
9	chr19:35737800-35738600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
10	chr19:35738000-35738400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
11	chr19:35738000-35738400	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
12	chr19:35738000-35738400	Enhancers	Duodenum Mucosa	Duodenum
13	chr19:35738000-35738400	Enhancers	Fetal Intestine Large	intestine
14	chr19:35738000-35738400	Enhancers	Fetal Intestine Small	intestine
15	chr19:35738000-35738400	Enhancers	Rectal Mucosa Donor 31	rectum
16	chr19:35738000-35738400	Enhancers	HepG2	liver
17	chr19:35738000-35738600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
18	chr19:35738000-35738600	Bivalent/Poised TSS	Thymus	Thymus
19	chr19:35738000-35739400	Weak transcription	Fetal Heart	heart
20	chr19:35738000-35740800	Active TSS	H1 Cell Line	embryonic stem cell
21	chr19:35738000-35741000	Active TSS	iPS-20b Cell Line	embryonic stem cell
22	chr19:35738200-35738400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr19:35738200-35738400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr19:35738200-35738400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr19:35738200-35738400	Flanking Bivalent TSS/Enh	Primary B cells from cord blood	blood
26	chr19:35738200-35738400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
27	chr19:35738200-35738400	Enhancers	Primary T helper cells fromperipheralblood	blood
28	chr19:35738200-35738400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr19:35738200-35738400	Enhancers	Liver	Liver
30	chr19:35738200-35738400	Enhancers	Colonic Mucosa	Colon
31	chr19:35738200-35738400	Enhancers	Pancreas	Pancrea
32	chr19:35738200-35738400	Active TSS	Rectal Mucosa Donor 29	rectum
33	chr19:35738200-35738400	Enhancers	GM12878-XiMat	blood
34	chr19:35738200-35738400	Enhancers	NHEK	skin
35	chr19:35738200-35738600	Enhancers	Primary B cells from peripheral blood	blood
36	chr19:35738200-35738600	Flanking Active TSS	K562	blood
37	chr19:35738200-35738800	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
38	chr19:35738200-35740600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
39	chr19:35738200-35740800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
40	chr19:35738200-35740800	Active TSS	HUES6 Cell Line	embryonic stem cell
41	chr19:35738200-35741000	Bivalent/Poised TSS	Fetal Kidney	kidney
42	chr19:35738200-35741400	Active TSS	ES-I3 Cell Line	embryonic stem cell
43	chr19:35738400-35738600	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr19:35738400-35738600	Bivalent Enhancer	Primary B cells from cord blood	blood
45	chr19:35738400-35738600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
46	chr19:35738400-35738600	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
47	chr19:35738400-35738600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
48	chr19:35738400-35738600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
49	chr19:35738400-35738600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
50	chr19:35738400-35738600	Enhancers	Primary T killer naive cells fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links