Variant report

Variant	rs934826
Chromosome Location	chr2:127825968-127825969
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:76)
CpG islands
(count:61)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:76 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MAX	chr2:127825427-127826003	HepG2	liver:	n/a	chr2:127825925-127825934
2	MAZ	chr2:127825444-127826090	IMR90	lung:	n/a	chr2:127825925-127825934
3	RAD21	chr2:127825395-127826254	SK-N-SH	brain:	n/a	n/a
4	BHLHE40	chr2:127825385-127825984	HepG2	liver:	n/a	n/a
5	RAD21	chr2:127825556-127826026	H1-hESC	embryonic stem cell:	n/a	n/a
6	RAD21	chr2:127825565-127826033	SK-N-SH_RA	brain:	n/a	n/a
7	NR2F2	chr2:127825402-127826065	K562	blood:	n/a	n/a
8	JUND	chr2:127825186-127825969	K562	blood:	n/a	n/a
9	SMC3	chr2:127825606-127825993	K562	blood:	n/a	n/a
10	RAD21	chr2:127825377-127826255	HCT-116	colon:	n/a	n/a
11	E2F6	chr2:127825206-127826020	H1-hESC	embryonic stem cell:	n/a	n/a
12	RAD21	chr2:127825605-127825974	Hela-S3	cervix:	n/a	n/a
13	GABPA	chr2:127825487-127825978	MCF-7	breast:	n/a	n/a
14	BHLHE40	chr2:127825293-127825973	K562	blood:	n/a	n/a
15	CTCF	chr2:127825622-127825988	HepG2	liver:	n/a	n/a
16	USF1	chr2:127825490-127825992	ECC-1	luminal epithelium:	n/a	n/a
17	SMC3	chr2:127825606-127825997	GM12878	blood:	n/a	n/a
18	MAX	chr2:127825488-127826037	MCF-7	breast:	n/a	chr2:127825925-127825934
19	RAD21	chr2:127825569-127825985	ECC-1	luminal epithelium:	n/a	n/a
20	RAD21	chr2:127825543-127826097	A549	lung:	n/a	n/a
21	RAD21	chr2:127825498-127826104	ECC-1	luminal epithelium:	n/a	n/a
22	RAD21	chr2:127825477-127826048	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr2:127825587-127825985	A549	lung:	n/a	n/a
24	ZNF143	chr2:127825609-127825977	GM12878	blood:	n/a	n/a
25	ZNF143	chr2:127825603-127825979	H1-hESC	embryonic stem cell:	n/a	n/a
26	MAX	chr2:127825370-127826000	H1-hESC	embryonic stem cell:	n/a	chr2:127825925-127825934
27	SMC3	chr2:127825168-127826193	SK-N-SH	brain:	n/a	n/a
28	CTCF	chr2:127825571-127825995	IMR90	lung:	n/a	n/a
29	CTCF	chr2:127825599-127826135	K562	blood:	n/a	n/a
30	RAD21	chr2:127825578-127825978	HepG2	liver:	n/a	n/a
31	RAD21	chr2:127825430-127826057	IMR90	lung:	n/a	n/a
32	ATF2	chr2:127825499-127825993	H1-hESC	embryonic stem cell:	n/a	n/a
33	USF1	chr2:127825312-127826007	HCT-116	colon:	n/a	n/a
34	ELF1	chr2:127825435-127826020	MCF-7	breast:	n/a	n/a
35	CTCF	chr2:127825606-127826007	K562	blood:	n/a	n/a
36	GTF2F1	chr2:127825603-127825971	H1-hESC	embryonic stem cell:	n/a	n/a
37	TCF12	chr2:127825434-127826023	A549	lung:	n/a	n/a
38	RAD21	chr2:127825545-127826023	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr2:127825607-127825976	SK-N-SH_RA	brain:	n/a	n/a
40	CTCF	chr2:127825371-127826160	HCT-116	colon:	n/a	n/a
41	CTCF	chr2:127825333-127826182	A549	lung:	n/a	n/a
42	CTCF	chr2:127825613-127825979	GM12891	blood:	n/a	n/a
43	POLR2A	chr2:127825801-127826006	GM12878	blood:	n/a	n/a
44	MAX	chr2:127825351-127826093	HCT-116	colon:	n/a	chr2:127825925-127825934
45	RAD21	chr2:127825633-127826001	GM12878	blood:	n/a	n/a
46	RAD21	chr2:127825570-127825986	HepG2	liver:	n/a	n/a
47	MAZ	chr2:127825440-127825978	K562	blood:	n/a	chr2:127825925-127825934
48	JUN	chr2:127825008-127826098	K562	blood:	n/a	n/a
49	MAX	chr2:127825175-127825968	K562	blood:	n/a	chr2:127825925-127825934
50	SMC3	chr2:127825455-127825988	Hela-S3	cervix:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:127825935-127825985	HAEpiC	amniotic membrane:	n/a
2	chr2:127825935-127825985	HCM	heart:	n/a
3	chr2:127825935-127825985	HIPEpiC	eye:	n/a
4	chr2:127825935-127825985	CMK	blood:	n/a
5	chr2:127825935-127825985	AG04449	skin:	fetal
6	chr2:127825935-127825985	PrEC	prostate:	n/a
7	chr2:127825935-127825985	ovcar-3	ovarian:	n/a
8	chr2:127825935-127825985	K562	blood:	n/a
9	chr2:127825935-127825985	HCPEpiC	choroid plexus:	n/a
10	chr2:127825935-127825985	AG09319	gingival:	n/a
11	chr2:127825935-127825985	NHDF-neo	bronchial:	n/a
12	chr2:127825935-127825985	NH-A	brain:	n/a
13	chr2:127825935-127825985	ProgFib	skin:	n/a
14	chr2:127825935-127825985	HepG2	liver:	n/a
15	chr2:127825935-127825985	T-47D	breast:	n/a
16	chr2:127825935-127825985	PANC-1	pancreas:	n/a
17	chr2:127825935-127825985	HCT-116	colon:	n/a
18	chr2:127825935-127825985	IMR90	lung:	fetal
19	chr2:127825935-127825985	BJ	skin:	n/a
20	chr2:127825935-127825985	ECC-1	luminal epithelium:	n/a
21	chr2:127825935-127825985	GM12891	blood:	n/a
22	chr2:127825935-127825985	GM06990	blood:	n/a
23	chr2:127825935-127825985	GM12878	blood:	n/a
24	chr2:127825935-127825985	Caco-2	colon:	n/a
25	chr2:127825935-127825985	SKMC	muscle:	n/a
26	chr2:127825935-127825985	HMEC	breast:	n/a
27	chr2:127825935-127825985	LNCaP	prostate:	n/a
28	chr2:127825935-127825985	U87	brain:	n/a
29	chr2:127825935-127825985	HNPCEpiC	eye:	n/a
30	chr2:127825935-127825985	Hepatocyte	liver:	n/a
31	chr2:127825935-127825985	NHBE	bronchial:	n/a
32	chr2:127825935-127825985	SK-N-SH_RA	brain:	n/a
33	chr2:127825935-127825985	HRPEpiC	eye:	n/a
34	chr2:127825935-127825985	GM12892	blood:	n/a
35	chr2:127825935-127825985	HPAEpiC	pulmonary alveolar:	n/a
36	chr2:127825935-127825985	Hela-S3	cervix:	n/a
37	chr2:127825935-127825985	HCF	heart:	n/a
38	chr2:127825935-127825985	AG04450	lung:	fetal
39	chr2:127825935-127825985	MCF-7	breast:	n/a
40	chr2:127825935-127825985	A549	lung:	n/a
41	chr2:127825935-127825985	MCF10A-Er-Src	breast:	n/a
42	chr2:127825935-127825985	AG10803	skin:	n/a
43	chr2:127825935-127825985	SAEC	small airway:	n/a
44	chr2:127825935-127825985	HL-60	blood:	n/a
45	chr2:127825935-127825985	SK-N-MC	brain:	n/a
46	chr2:127825935-127825985	NT2-D1	testis:	n/a
47	chr2:127825935-127825985	HEEpiC	esophagus:	n/a
48	chr2:127825935-127825985	HUVEC	blood vessel:	n/a
49	chr2:127825935-127825985	NB4	blood:	n/a
50	chr2:127825935-127825985	GM19239	blood:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:127825651..127827427-chr2:127830304..127832432,2	MCF-7	breast:
2	chr2:127825705..127826883-chr2:127897059..127898198,8	MCF-7	breast:
3	chr2:127825353..127826710-chr2:127931463..127932268,5	MCF-7	breast:
4	chr2:127824897..127826990-chr2:127827722..127829890,2	K562	blood:
5	chr2:127825662..127826505-chr2:127954218..127955183,2	MCF-7	breast:
6	chr2:127819816..127822749-chr2:127823381..127826394,3	K562	blood:
7	chr2:127825712..127826261-chr2:127901784..127902300,2	MCF-7	breast:
8	chr2:127820803..127824621-chr2:127824894..127830047,6	K562	blood:
9	chr2:127825223..127826267-chr2:127857805..127858865,3	MCF-7	breast:
10	chr2:127825460..127825985-chr2:127931746..127932330,2	MCF-7	breast:
11	chr2:127825324..127826896-chr2:127856890..127859750,2	MCF-7	breast:
12	chr2:127825650..127826234-chr2:127897075..127897865,2	MCF-7	breast:

No data

Variant related genes	Relation type
BIN1	TF binding region
BIN1	CpG island
ENSG00000136717	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:29 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv999422	chr2:127464647-127956543	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv1004930	chr2:127477369-127938234	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv459230	chr2:127771006-127844735	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv583032	chr2:127771006-127844735	Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1003730	chr2:127794288-127860830	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
6	nsv1003461	chr2:127794288-127862257	Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv516759	chr2:127796666-127859441	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
8	nsv1000994	chr2:127797089-127860830	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
9	esv1825024	chr2:127798138-127864285	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv459241	chr2:127800981-127868435	Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
11	nsv583033	chr2:127800981-127868435	Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
12	nsv875011	chr2:127800981-127868435	Genic enhancers Flanking Active TSS Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
13	nsv875012	chr2:127800981-127895573	Enhancers ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
14	nsv1002673	chr2:127801964-127860830	Enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
15	nsv1010577	chr2:127801964-127862257	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
16	nsv1011224	chr2:127802375-127860830	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
17	nsv1003887	chr2:127802375-127862257	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
18	nsv1009309	chr2:127802730-127862257	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
19	nsv1014290	chr2:127805366-127860830	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
20	nsv1010084	chr2:127805366-127862257	Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
21	nsv997855	chr2:127806424-127857946	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
22	nsv1001673	chr2:127810478-127858634	Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
23	nsv1002124	chr2:127810478-127860830	Strong transcription Genic enhancers Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
24	nsv1005423	chr2:127814781-127857751	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
25	nsv997847	chr2:127814781-127858634	Flanking Active TSS Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
26	nsv1014118	chr2:127814781-127860830	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
27	nsv583034	chr2:127821207-127828394	Strong transcription Enhancers Flanking Active TSS Genic enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
28	nsv999224	chr2:127821207-127860830	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
29	nsv583035	chr2:127825968-127844735	Genic enhancers Flanking Active TSS Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:109 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:127808600-127834200	Strong transcription	Primary T cells from cord blood	blood
2	chr2:127815200-127850800	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr2:127815400-127826600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr2:127816000-127829000	Weak transcription	Aorta	Aorta
5	chr2:127816600-127829600	Weak transcription	Brain Germinal Matrix	brain
6	chr2:127816800-127831200	Weak transcription	Fetal Brain Female	brain
7	chr2:127817200-127833800	Genic enhancers	Spleen	Spleen
8	chr2:127818400-127844400	Genic enhancers	Fetal Muscle Leg	muscle
9	chr2:127821000-127827200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr2:127821200-127838600	Genic enhancers	Fetal Muscle Trunk	muscle
11	chr2:127821600-127826000	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr2:127821800-127826400	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr2:127821800-127829200	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
14	chr2:127821800-127830000	Genic enhancers	Brain Substantia Nigra	brain
15	chr2:127821800-127830200	Genic enhancers	Brain Inferior Temporal Lobe	brain
16	chr2:127822000-127826400	Genic enhancers	Primary T cells fromperipheralblood	blood
17	chr2:127822000-127830200	Genic enhancers	Brain Cingulate Gyrus	brain
18	chr2:127822200-127829600	Genic enhancers	Brain Anterior Caudate	brain
19	chr2:127822400-127826400	Enhancers	Adipose Nuclei	Adipose
20	chr2:127822800-127836600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr2:127822800-127836800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr2:127823000-127829800	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr2:127823000-127832800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr2:127823200-127826000	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr2:127823200-127826800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr2:127823200-127830600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr2:127823200-127831800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr2:127823200-127832600	Weak transcription	GM12878-XiMat	blood
29	chr2:127823200-127838200	Weak transcription	Left Ventricle	heart
30	chr2:127823400-127826000	Enhancers	Skeletal Muscle Female	skeletal muscle
31	chr2:127823400-127826200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr2:127823400-127826800	Weak transcription	Primary B cells from cord blood	blood
33	chr2:127823400-127839200	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr2:127823600-127826000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr2:127823600-127826000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr2:127823600-127827000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
37	chr2:127823600-127838800	Weak transcription	Fetal Kidney	kidney
38	chr2:127823800-127826000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr2:127824000-127838400	Weak transcription	Rectal Smooth Muscle	rectum
40	chr2:127824200-127826200	Enhancers	Colonic Mucosa	Colon
41	chr2:127824800-127826000	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr2:127824800-127826000	Genic enhancers	Fetal Intestine Small	intestine
43	chr2:127824800-127826400	Genic enhancers	Placenta	Placenta
44	chr2:127824800-127830000	Genic enhancers	Brain Dorsolateral Prefrontal Cortex	brain
45	chr2:127824800-127830400	Genic enhancers	Brain Angular Gyrus	brain
46	chr2:127825000-127826000	Genic enhancers	Stomach Smooth Muscle	stomach
47	chr2:127825000-127826000	Enhancers	A549	lung
48	chr2:127825000-127826200	Enhancers	Right Ventricle	heart
49	chr2:127825000-127827000	Genic enhancers	Gastric	stomach
50	chr2:127825000-127830400	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links