Variant report

Variant	rs12693155
Chromosome Location	chr2:179058714-179058715
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:116)
CpG islands
(count:61)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:116 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ELK1	chr2:179058650-179058755	Hela-S3	cervix:	n/a	n/a
2	RAD21	chr2:179058557-179059494	IMR90	lung:	n/a	chr2:179059002-179059012 chr2:179058967-179058977 chr2:179059478-179059492
3	POLR2A	chr2:179058538-179059525	Hela-S3	cervix:	n/a	n/a
4	POLR2A	chr2:179058666-179059421	A549	lung:	n/a	n/a
5	POLR2A	chr2:179058566-179058836	Hela-S3	cervix:	n/a	n/a
6	MAX	chr2:179058449-179060229	K562	blood:	n/a	chr2:179060029-179060039
7	CEBPB	chr2:179058054-179058776	HepG2	liver:	n/a	n/a
8	TBP	chr2:179058450-179058824	H1-hESC	embryonic stem cell:	n/a	n/a
9	RCOR1	chr2:179058459-179060393	K562	blood:	n/a	n/a
10	CHD1	chr2:179058524-179059060	H1-hESC	embryonic stem cell:	n/a	n/a
11	POLR2A	chr2:179058624-179059568	Gliobla	brain:	n/a	n/a
12	CEBPB	chr2:179058590-179058717	H1-hESC	embryonic stem cell:	n/a	n/a
13	ZBTB7A	chr2:179058652-179060286	ECC-1	luminal epithelium:	n/a	n/a
14	TCF7L2	chr2:179058284-179059180	Hela-S3	cervix:	n/a	chr2:179058537-179058546
15	YY1	chr2:179058680-179059549	HepG2	liver:	n/a	chr2:179058780-179058791 chr2:179059042-179059056
16	GATA2	chr2:179058411-179060151	SH-SY5Y	brain:	n/a	n/a
17	GATA3	chr2:179058108-179058756	MCF-7	breast:	n/a	n/a
18	MAX	chr2:179058157-179059462	Hela-S3	cervix:	n/a	n/a
19	REST	chr2:179058676-179059075	ECC-1	luminal epithelium:	n/a	n/a
20	HDAC2	chr2:179058147-179058964	HepG2	liver:	n/a	n/a
21	YY1	chr2:179058583-179059478	ECC-1	luminal epithelium:	n/a	chr2:179058780-179058791 chr2:179059042-179059056
22	CTCF	chr2:179058680-179058830	HEK293	kidney:	n/a	n/a
23	FOXA1	chr2:179058044-179058751	HepG2	liver:	n/a	n/a
24	TCF7L2	chr2:179058383-179058830	PANC-1	pancreas:	n/a	chr2:179058537-179058546
25	SMARCB1	chr2:179058328-179060261	Hela-S3	cervix:	n/a	n/a
26	MAZ	chr2:179058111-179060371	IMR90	lung:	n/a	chr2:179060029-179060039
27	CTBP2	chr2:179058381-179060303	H1-hESC	embryonic stem cell:	n/a	n/a
28	FOXA2	chr2:179058215-179058753	A549	lung:	n/a	n/a
29	ELF1	chr2:179058661-179059750	K562	blood:	n/a	chr2:179059477-179059486
30	CREB1	chr2:179058042-179058792	HepG2	liver:	n/a	n/a
31	NRF1	chr2:179058681-179060459	SK-N-SH	brain:	n/a	chr2:179059845-179059854 chr2:179059063-179059074
32	ZNF263	chr2:179058600-179060135	K562	blood:	n/a	n/a
33	TAF1	chr2:179058595-179058806	H1-hESC	embryonic stem cell:	n/a	n/a
34	ZKSCAN1	chr2:179058378-179059344	Hela-S3	cervix:	n/a	n/a
35	E2F4	chr2:179058412-179060224	K562	blood:	n/a	chr2:179059845-179059854 chr2:179059989-179059999 chr2:179059739-179059749
36	ZNF263	chr2:179058255-179060384	HEK293-T-REx	kidney:	n/a	chr2:179060154-179060163
37	POLR2A	chr2:179058298-179060218	Hela-S3	cervix:	n/a	n/a
38	TCF12	chr2:179058668-179060170	ECC-1	luminal epithelium:	n/a	chr2:179059872-179059879 chr2:179059998-179060008
39	TBL1XR1	chr2:179058566-179059512	K562	blood:	n/a	n/a
40	MXI1	chr2:179058183-179060504	IMR90	lung:	n/a	n/a
41	HA-E2F1	chr2:179058141-179060307	MCF-7	breast:	n/a	chr2:179059845-179059854 chr2:179059117-179059128 chr2:179059090-179059101 chr2:179059989-179059999 chr2:179059739-179059749
42	POLR2A	chr2:179058501-179060192	MCF-7	breast:	n/a	n/a
43	TAF1	chr2:179058506-179060229	ECC-1	luminal epithelium:	n/a	n/a
44	UBTF	chr2:179058297-179060341	K562	blood:	n/a	n/a
45	E2F1	chr2:179058629-179060052	Hela-S3	cervix:	n/a	chr2:179059845-179059854 chr2:179059117-179059128 chr2:179059090-179059101 chr2:179059989-179059999 chr2:179059739-179059749
46	TBP	chr2:179058700-179060198	K562	blood:	n/a	n/a
47	BACH1	chr2:179058627-179059213	H1-hESC	embryonic stem cell:	n/a	n/a
48	SP4	chr2:179058669-179058916	H1-hESC	embryonic stem cell:	n/a	n/a
49	POLR2A	chr2:179058450-179059583	Hela-S3	cervix:	n/a	n/a
50	POLR2A	chr2:179058656-179059573	SK-N-MC	brain:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:179058698-179058748	Hepatocyte	liver:	n/a
2	chr2:179058698-179058748	NHBE	bronchial:	n/a
3	chr2:179058698-179058748	MCF10A-Er-Src	breast:	n/a
4	chr2:179058698-179058748	NHDF-neo	bronchial:	n/a
5	chr2:179058698-179058748	HRCEpiC	kidney:	n/a
6	chr2:179058698-179058748	HL-60	blood:	n/a
7	chr2:179058698-179058748	HPAEpiC	pulmonary alveolar:	n/a
8	chr2:179058698-179058748	HRE	kidney:	n/a
9	chr2:179058698-179058748	PrEC	prostate:	n/a
10	chr2:179058698-179058748	GM06990	blood:	n/a
11	chr2:179058698-179058748	CMK	blood:	n/a
12	chr2:179058698-179058748	ProgFib	skin:	n/a
13	chr2:179058698-179058748	HRPEpiC	eye:	n/a
14	chr2:179058698-179058748	HMEC	breast:	n/a
15	chr2:179058698-179058748	MCF-7	breast:	n/a
16	chr2:179058698-179058748	AG04450	lung:	fetal
17	chr2:179058698-179058748	NB4	blood:	n/a
18	chr2:179058698-179058748	K562	blood:	n/a
19	chr2:179058698-179058748	AoSMC	blood vessel:	n/a
20	chr2:179058698-179058748	U87	brain:	n/a
21	chr2:179058698-179058748	GM12891	blood:	n/a
22	chr2:179058698-179058748	H1-hESC	embryonic stem cell:	embryo
23	chr2:179058698-179058748	AG04449	skin:	fetal
24	chr2:179058698-179058748	NH-A	brain:	n/a
25	chr2:179058698-179058748	Jurkat	blood:	n/a
26	chr2:179058698-179058748	HCF	heart:	n/a
27	chr2:179058698-179058748	HNPCEpiC	eye:	n/a
28	chr2:179058698-179058748	AG09319	gingival:	n/a
29	chr2:179058698-179058748	HCPEpiC	choroid plexus:	n/a
30	chr2:179058698-179058748	GM19239	blood:	n/a
31	chr2:179058698-179058748	Hela-S3	cervix:	n/a
32	chr2:179058698-179058748	Caco-2	colon:	n/a
33	chr2:179058698-179058748	PANC-1	pancreas:	n/a
34	chr2:179058698-179058748	HUVEC	blood vessel:	n/a
35	chr2:179058698-179058748	GM12892	blood:	n/a
36	chr2:179058698-179058748	SKMC	muscle:	n/a
37	chr2:179058698-179058748	HAEpiC	amniotic membrane:	n/a
38	chr2:179058698-179058748	HCM	heart:	n/a
39	chr2:179058698-179058748	T-47D	breast:	n/a
40	chr2:179058698-179058748	HIPEpiC	eye:	n/a
41	chr2:179058698-179058748	BE2_C	brain:	n/a
42	chr2:179058698-179058748	SAEC	small airway:	n/a
43	chr2:179058698-179058748	AG10803	skin:	n/a
44	chr2:179058698-179058748	ovcar-3	ovarian:	n/a
45	chr2:179058698-179058748	SK-N-MC	brain:	n/a
46	chr2:179058698-179058748	RPTEC	kidney:	n/a
47	chr2:179058698-179058748	SK-N-SH	brain:	n/a
48	chr2:179058698-179058748	HEEpiC	esophagus:	n/a
49	chr2:179058698-179058748	SK-N-SH_RA	brain:	n/a
50	chr2:179058698-179058748	LNCaP	prostate:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:178976797..178977610-chr2:179058506..179059074,2	MCF-7	breast:
2	chr2:178975067..178978289-chr2:179058254..179060575,4	MCF-7	breast:
3	chr2:179057756..179060082-chr2:179314891..179318046,3	MCF-7	breast:
4	chr2:178975761..178978600-chr2:179056476..179059620,3	K562	blood:
5	chr2:179056933..179060923-chr2:179315358..179318702,4	MCF-7	breast:

No data

Variant related genes	Relation type
OSBPL6	TF binding region
OSBPL6	CpG island
ENSG00000204311	Chromatin interaction
ENSG00000180228	Chromatin interaction
ENSG00000155636	Chromatin interaction

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs12471750	0.80[ASN][1000 genomes]
rs13389850	0.85[ASN][1000 genomes]
rs17638592	0.89[ASN][1000 genomes]
rs186736	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs232042	0.93[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs2366365	0.84[ASN][1000 genomes]
rs3099472	0.91[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs334079	0.91[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs334080	0.92[AFR][1000 genomes];0.88[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs334081	0.93[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs334092	0.84[ASN][1000 genomes]
rs334094	0.87[ASN][1000 genomes]
rs334102	0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs334103	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs334115	0.89[ASN][1000 genomes]
rs334116	0.92[AFR][1000 genomes];0.82[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs334117	0.90[ASN][1000 genomes]
rs334122	0.83[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs334125	0.98[AFR][1000 genomes];0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs334126	0.87[ASN][1000 genomes]
rs334128	0.89[AFR][1000 genomes];0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs334132	0.87[ASN][1000 genomes]
rs334133	0.85[ASN][1000 genomes]
rs437523	0.87[ASN][1000 genomes]
rs4894001	0.82[ASN][1000 genomes]
rs7591476	0.82[ASN][1000 genomes]
rs7595650	0.88[ASN][1000 genomes]
rs930191	0.94[AFR][1000 genomes];0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1009312	chr2:178924318-179215566	Weak transcription Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv536057	chr2:178924318-179215566	Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Enhancers Flanking Active 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	11 gene(s)	inside rSNPs	diseases
3	nsv875452	chr2:178963445-179167766	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv875453	chr2:179022751-179060313	Flanking Active TSS Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv875454	chr2:179022751-179066443	Bivalent/Poised TSS Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	esv3340257	chr2:179057106-179061404	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	esv17391	chr2:179058529-179059941	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	esv3409926	chr2:179058531-179061079	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	esv1821975	chr2:179058577-179059878	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	esv1834988	chr2:179058577-179059878	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	esv1838690	chr2:179058577-179060313	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	esv1841516	chr2:179058577-179060313	Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
13	nsv583740	chr2:179058681-179059599	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
14	nsv583741	chr2:179058681-179059658	Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
15	nsv583742	chr2:179058681-179059878	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
16	nsv583743	chr2:179058714-179059658	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
17	esv1802318	chr2:179058714-179059878	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
18	esv1839900	chr2:179058714-179059878	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
19	nsv583744	chr2:179058714-179059878	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr2:179058000-179058800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr2:179058000-179058800	Flanking Active TSS	Adipose Nuclei	Adipose
3	chr2:179058000-179058800	Flanking Active TSS	Liver	Liver
4	chr2:179058000-179058800	Flanking Active TSS	Stomach Smooth Muscle	stomach
5	chr2:179058000-179058800	Flanking Active TSS	NHEK	skin
6	chr2:179058000-179059000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
7	chr2:179058000-179060800	Active TSS	NHLF	lung
8	chr2:179058000-179061200	Active TSS	Brain Angular Gyrus	brain
9	chr2:179058200-179058800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells	blood
10	chr2:179058200-179058800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr2:179058200-179058800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr2:179058200-179058800	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
13	chr2:179058200-179058800	Bivalent/Poised TSS	Small Intestine	intestine
14	chr2:179058200-179058800	Flanking Active TSS	HMEC	breast
15	chr2:179058200-179059000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
16	chr2:179058200-179059000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
17	chr2:179058200-179059200	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
18	chr2:179058200-179059400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr2:179058200-179059800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr2:179058200-179060400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
21	chr2:179058200-179060400	Active TSS	Colon Smooth Muscle	Colon
22	chr2:179058200-179060400	Active TSS	Left Ventricle	heart
23	chr2:179058200-179060400	Active TSS	Rectal Smooth Muscle	rectum
24	chr2:179058200-179060600	Active TSS	Right Ventricle	heart
25	chr2:179058200-179060600	Active TSS	NHDF-Ad	bronchial
26	chr2:179058200-179060800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr2:179058200-179060800	Active TSS	Right Atrium	heart
28	chr2:179058200-179061000	Active TSS	Pancreatic Islets	Pancreatic Islet
29	chr2:179058400-179058800	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr2:179058400-179058800	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
31	chr2:179058400-179058800	Flanking Bivalent TSS/Enh	Primary monocytes fromperipheralblood	blood
32	chr2:179058400-179058800	Bivalent Enhancer	Primary B cells from peripheral blood	blood
33	chr2:179058400-179058800	Flanking Bivalent TSS/Enh	Primary T cells from cord blood	blood
34	chr2:179058400-179058800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
35	chr2:179058400-179058800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
36	chr2:179058400-179058800	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
37	chr2:179058400-179058800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
38	chr2:179058400-179058800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
39	chr2:179058400-179058800	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr2:179058400-179058800	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
41	chr2:179058400-179058800	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
42	chr2:179058400-179058800	Flanking Bivalent TSS/Enh	Placenta	Placenta
43	chr2:179058400-179058800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
44	chr2:179058400-179058800	Enhancers	Spleen	Spleen
45	chr2:179058400-179058800	Flanking Bivalent TSS/Enh	GM12878-XiMat	blood
46	chr2:179058400-179059000	Flanking Bivalent TSS/Enh	Primary T helper cells fromperipheralblood	blood
47	chr2:179058400-179059000	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
48	chr2:179058400-179059000	Flanking Bivalent TSS/Enh	HepG2	liver
49	chr2:179058400-179059000	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
50	chr2:179058400-179059200	Active TSS	Colonic Mucosa	Colon

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