Variant report

Variant	nsv1013513
Chromosome Location	chr2:113876914-113893482
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:258)
CpG islands
(count:428)
Chromatin interactive
region (count:23)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:258 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:113882669-113883313	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:113883762-113884126	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:113884339-113885187	HepG2	liver:	n/a	n/a
4	ATF2	chr2:113881686-113882473	GM12878	blood:	n/a	n/a
5	ATF2	chr2:113881990-113882439	GM12878	blood:	n/a	n/a
6	ATF3	chr2:113888961-113889164	K562	blood:	n/a	n/a
7	BATF	chr2:113881700-113882056	GM12878	blood:	n/a	n/a
8	BHLHE40	chr2:113893094-113893119	GM12878	blood:	n/a	n/a
9	BHLHE40	chr2:113881779-113882462	GM12878	blood:	n/a	n/a
10	BHLHE40	chr2:113882094-113882360	A549	lung:	n/a	n/a
11	BHLHE40	chr2:113882006-113882356	HepG2	liver:	n/a	n/a
12	BHLHE40	chr2:113881739-113882336	K562	blood:	n/a	n/a
13	BHLHE40	chr2:113884403-113885067	HepG2	liver:	n/a	n/a
14	BRCA1	chr2:113885012-113885189	HepG2	liver:	n/a	n/a
15	BRCA1	chr2:113884482-113884716	HepG2	liver:	n/a	n/a
16	CEBPB	chr2:113892082-113892372	HepG2	liver:	n/a	chr2:113892209-113892220 chr2:113892209-113892222
17	CEBPB	chr2:113884942-113885118	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr2:113892146-113892362	A549	lung:	n/a	chr2:113892209-113892220 chr2:113892209-113892222
19	CEBPB	chr2:113882095-113882379	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr2:113884358-113885254	HepG2	liver:	n/a	n/a
21	CEBPB	chr2:113884447-113885219	HepG2	liver:	n/a	n/a
22	CEBPB	chr2:113884471-113885154	HepG2	liver:	n/a	n/a
23	CEBPB	chr2:113882131-113882330	IMR90	lung:	n/a	n/a
24	CEBPB	chr2:113884898-113885154	K562	blood:	n/a	n/a
25	CEBPB	chr2:113892187-113892248	IMR90	lung:	n/a	chr2:113892209-113892220 chr2:113892209-113892222
26	CEBPB	chr2:113882148-113882290	HepG2	liver:	n/a	n/a
27	CEBPB	chr2:113884887-113885162	A549	lung:	n/a	n/a
28	CEBPB	chr2:113884416-113885310	HepG2	liver:	n/a	n/a
29	CEBPD	chr2:113884457-113885105	HepG2	liver:	n/a	n/a
30	CHD2	chr2:113884438-113885225	HepG2	liver:	n/a	n/a
31	CTCF	chr2:113888336-113888420	GM20000	blood:	n/a	n/a
32	CTCF	chr2:113892960-113893110	WI-38	lung:	n/a	n/a
33	CTCF	chr2:113885014-113885044	GM12878	blood:	n/a	n/a
34	CTCF	chr2:113891340-113891490	HEK293	kidney:	n/a	n/a
35	CTCF	chr2:113884940-113885090	NB4	blood:	n/a	n/a
36	CTCF	chr2:113884986-113885074	HepG2	liver:	n/a	n/a
37	CTCF	chr2:113884880-113885030	GM06990	blood:	n/a	n/a
38	CTCF	chr2:113888179-113888240	GM10248	blood:	n/a	n/a
39	CTCF	chr2:113877053-113877085	LNCaP	prostate:	n/a	n/a
40	CTCF	chr2:113888291-113888358	Pancreas_OC	pancreas:	n/a	n/a
41	EBF1	chr2:113881958-113882459	GM12878	blood:	n/a	n/a
42	EBF1	chr2:113892626-113892857	GM12878	blood:	n/a	chr2:113892717-113892728 chr2:113892718-113892727 chr2:113892716-113892729
43	EGR1	chr2:113881782-113881963	GM12878	blood:	n/a	n/a
44	ELF1	chr2:113884466-113884787	HepG2	liver:	n/a	n/a
45	ELF1	chr2:113884859-113885249	HepG2	liver:	n/a	n/a
46	EP300	chr2:113884269-113885346	HepG2	liver:	n/a	n/a
47	EP300	chr2:113884370-113885171	HepG2	liver:	n/a	n/a
48	EP300	chr2:113882587-113883411	HepG2	liver:	n/a	chr2:113883330-113883346 chr2:113883356-113883365
49	EP300	chr2:113884157-113885301	HepG2	liver:	n/a	n/a
50	EP300	chr2:113882165-113882365	GM12878	blood:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:113885838-113885888	SK-N-MC	brain:	n/a
2	chr2:113885838-113885888	SK-N-MC	brain:	n/a
3	chr2:113885116-113885166	NB4	blood:	n/a
4	chr2:113884734-113884784	HRPEpiC	eye:	n/a
5	chr2:113885116-113885166	BE2_C	brain:	n/a
6	chr2:113885116-113885166	AG09319	gingival:	n/a
7	chr2:113885277-113885327	SK-N-SH	brain:	n/a
8	chr2:113884447-113884497	HEEpiC	esophagus:	n/a
9	chr2:113884376-113884426	AG04449	skin:	fetal
10	chr2:113884376-113884426	ProgFib	skin:	n/a
11	chr2:113884376-113884426	HL-60	blood:	n/a
12	chr2:113884734-113884784	Hepatocyte	liver:	n/a
13	chr2:113884447-113884497	HCT-116	colon:	n/a
14	chr2:113885116-113885166	NHDF-neo	bronchial:	n/a
15	chr2:113885277-113885327	HepG2	liver:	n/a
16	chr2:113885116-113885166	MCF10A-Er-Src	breast:	n/a
17	chr2:113884376-113884426	SAEC	small airway:	n/a
18	chr2:113884447-113884497	HMEC	breast:	n/a
19	chr2:113884447-113884497	AG10803	skin:	n/a
20	chr2:113885838-113885888	AoSMC	blood vessel:	n/a
21	chr2:113885116-113885166	SK-N-MC	brain:	n/a
22	chr2:113885116-113885166	HRE	kidney:	n/a
23	chr2:113885116-113885166	AoSMC	blood vessel:	n/a
24	chr2:113885277-113885327	SK-N-SH_RA	brain:	n/a
25	chr2:113884734-113884784	HepG2	liver:	n/a
26	chr2:113884376-113884426	Hepatocyte	liver:	n/a
27	chr2:113885838-113885888	AG09319	gingival:	n/a
28	chr2:113885116-113885166	LNCaP	prostate:	n/a
29	chr2:113884376-113884426	AG09309	skin:	n/a
30	chr2:113885838-113885888	H1-hESC	embryonic stem cell:	embryo
31	chr2:113884734-113884784	T-47D	breast:	n/a
32	chr2:113885277-113885327	MCF10A-Er-Src	breast:	n/a
33	chr2:113891507-113891557	HEK293	kidney:	embryo
34	chr2:113884734-113884784	K562	blood:	n/a
35	chr2:113891507-113891557	HepG2	liver:	n/a
36	chr2:113884734-113884784	MCF-7	breast:	n/a
37	chr2:113885116-113885166	IMR90	lung:	fetal
38	chr2:113891507-113891557	BE2_C	brain:	n/a
39	chr2:113885277-113885327	HIPEpiC	eye:	n/a
40	chr2:113884447-113884497	GM12878	blood:	n/a
41	chr2:113885838-113885888	GM12891	blood:	n/a
42	chr2:113884376-113884426	U87	brain:	n/a
43	chr2:113884447-113884497	HRE	kidney:	n/a
44	chr2:113884376-113884426	ovcar-3	ovarian:	n/a
45	chr2:113884447-113884497	PrEC	prostate:	n/a
46	chr2:113884734-113884784	GM06990	blood:	n/a
47	chr2:113884376-113884426	BJ	skin:	n/a
48	chr2:113885277-113885327	SAEC	small airway:	n/a
49	chr2:113885116-113885166	HMEC	breast:	n/a
50	chr2:113884734-113884784	AG04449	skin:	fetal

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:113874258..113877773-chr2:113883397..113886122,3	MCF-7	breast:
2	chr2:113888649..113891490-chr2:113893231..113895464,3	MCF-7	breast:
3	chr2:113882796..113885709-chr2:113913605..113916421,2	MCF-7	breast:
4	chr2:113876674..113878851-chr2:113881622..113884408,2	K562	blood:
5	chr2:113874258..113877773-chr2:113883397..113886122,3	MCF-7	breast:
6	chr2:113888649..113891490-chr2:113893231..113895464,3	MCF-7	breast:
7	chr2:113873018..113874918-chr2:113881727..113884531,2	MCF-7	breast:
8	chr2:113890813..113893082-chr2:113894067..113895922,2	MCF-7	breast:
9	chr2:113892912..113896093-chr2:113955457..113958866,4	MCF-7	breast:
10	chr2:113840365..113842107-chr2:113890479..113892989,2	MCF-7	breast:
11	chr2:113875025..113876736-chr2:113878416..113881099,2	MCF-7	breast:
12	chr2:113890768..113892944-chr2:113913806..113916135,2	MCF-7	breast:
13	chr2:113876674..113878851-chr2:113881622..113884408,2	K562	blood:
14	chr2:113881539..113883723-chr2:113885379..113887857,3	K562	blood:
15	chr2:113880075..113882309-chr2:113914138..113916361,2	MCF-7	breast:
16	chr2:113840523..113843293-chr2:113890844..113893174,3	MCF-7	breast:
17	chr2:113874395..113876014-chr2:113879125..113882509,3	K562	blood:
18	chr2:113835706..113838400-chr2:113880453..113883939,3	MCF-7	breast:
19	chr2:113885182..113887115-chr2:113914110..113915669,2	MCF-7	breast:
20	chr2:113881539..113883723-chr2:113885379..113887857,3	K562	blood:
21	chr2:113881134..113884097-chr2:113960459..113963321,2	K562	blood:
22	chr2:113840473..113842575-chr2:113882514..113884830,2	MCF-7	breast:
23	chr2:113863108..113865660-chr2:113875310..113877504,3	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PSD4-5	chr2:113885153-113885317	NONHSAT073745
2	lnc-PSD4-5	chr2:113887153-113887559	NONHSAT073745
3	lnc-PSD4-5	chr2:113885266-113885317	NONHSAT073743
4	lnc-PSD4-5	chr2:113887153-113887698	NONHSAT073743

No data

Variant related genes	Relation type
IL1RN	TF binding region
IL1RN	CpG island
ENSG00000125637	chromatin interactions
ENSG00000136689	chromatin interactions

Extended variants
information (count: 787 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:787 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143892994	chr2:113876953-113876954	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs4251983	chr2:113877019-113877020	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs2592346	chr2:113877023-113877024	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs571833838	chr2:113877026-113877027	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs534110071	chr2:113877032-113877033	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs75777405	chr2:113877091-113877092	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs139820346	chr2:113877128-113877129	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs566116256	chr2:113877143-113877144	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs551693526	chr2:113877169-113877170	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs193257295	chr2:113877198-113877199	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs4251984	chr2:113877226-113877227	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs556601754	chr2:113877259-113877260	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs576461849	chr2:113877279-113877280	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs143133759	chr2:113877318-113877319	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs182196722	chr2:113877342-113877343	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs555716220	chr2:113877382-113877383	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs146394349	chr2:113877389-113877390	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs4251985	chr2:113877413-113877414	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs79738955	chr2:113877418-113877419	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs371610116	chr2:113877474-113877475	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs186803334	chr2:113877481-113877482	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs45607539	chr2:113877482-113877483	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs928940	chr2:113877495-113877496	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs111233549	chr2:113877509-113877510	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs4251986	chr2:113877538-113877539	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs4251987	chr2:113877545-113877546	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs370057381	chr2:113877650-113877651	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs137932510	chr2:113877652-113877653	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs144607130	chr2:113877688-113877689	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs369994270	chr2:113877690-113877691	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs149439584	chr2:113877691-113877692	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs552080227	chr2:113877693-113877694	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs201934089	chr2:113877695-113877696	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs201759499	chr2:113877702-113877703	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs373740711	chr2:113877705-113877706	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs878972	chr2:113877713-113877714	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs370592421	chr2:113877724-113877725	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs56079611	chr2:113877730-113877731	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs547672505	chr2:113877773-113877774	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs567815115	chr2:113877789-113877790	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs536751320	chr2:113877799-113877800	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs191625422	chr2:113877802-113877803	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs45597637	chr2:113877832-113877833	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs116712258	chr2:113877838-113877839	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs539010814	chr2:113877881-113877882	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs558065852	chr2:113877891-113877892	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs55941815	chr2:113877898-113877899	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs35564162	chr2:113877902-113877903	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs4251988	chr2:113877917-113877918	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs530827396	chr2:113877918-113877919	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Colorectal cancer	16912164	CNVD
Ischaemic stroke	16980335	CNVD
Acute myeloid leukemia	18000384	CNVD
Nephronophthisis	17901113	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:299 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:113874200-113877200	Enhancers	Primary hematopoietic stem cells short term culture	blood
2	chr2:113874400-113877000	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr2:113874600-113877600	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr2:113874600-113878400	Weak transcription	GM12878-XiMat	blood
5	chr2:113874800-113878800	Weak transcription	Primary T helper cells fromperipheralblood	blood
6	chr2:113875000-113877000	Weak transcription	Small Intestine	intestine
7	chr2:113875000-113878600	Active TSS	Esophagus	oesophagus
8	chr2:113875400-113887400	Weak transcription	Spleen	Spleen
9	chr2:113875600-113878400	Weak transcription	Primary B cells from peripheral blood	blood
10	chr2:113875600-113881000	Weak transcription	Primary hematopoietic stem cells	blood
11	chr2:113875800-113877600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr2:113875800-113880800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr2:113875800-113881000	Weak transcription	Lung	lung
14	chr2:113876000-113877000	Weak transcription	Stomach Mucosa	stomach
15	chr2:113876000-113887400	Weak transcription	Gastric	stomach
16	chr2:113876000-113896200	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr2:113876200-113877200	Enhancers	HMEC	breast
18	chr2:113876200-113881400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr2:113876400-113877600	Flanking Active TSS	NHEK	skin
20	chr2:113876600-113877000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr2:113876600-113877200	Flanking Active TSS	Duodenum Mucosa	Duodenum
22	chr2:113876600-113877600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr2:113876600-113885000	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr2:113876800-113878600	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr2:113877000-113877200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr2:113877000-113877200	Enhancers	Sigmoid Colon	Sigmoid Colon
27	chr2:113877000-113877400	Enhancers	Small Intestine	intestine
28	chr2:113877000-113877600	Enhancers	Stomach Mucosa	stomach
29	chr2:113877200-113877800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr2:113877200-113877800	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr2:113877200-113880800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr2:113877200-113881600	Weak transcription	HMEC	breast
33	chr2:113877600-113877800	Enhancers	NHEK	skin
34	chr2:113877600-113878200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr2:113877600-113878800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr2:113877600-113879000	Weak transcription	Primary neutrophils fromperipheralblood	blood
37	chr2:113877600-113881600	Weak transcription	Stomach Mucosa	stomach
38	chr2:113877800-113878400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr2:113877800-113878800	Weak transcription	NHEK	skin
40	chr2:113878200-113878400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr2:113878400-113878600	Enhancers	Primary B cells from peripheral blood	blood
42	chr2:113878400-113878600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr2:113878400-113879000	Enhancers	GM12878-XiMat	blood
44	chr2:113878400-113879400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr2:113878600-113879000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
46	chr2:113878600-113879200	Weak transcription	Esophagus	oesophagus
47	chr2:113878600-113880200	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr2:113878800-113879000	Enhancers	Primary T helper cells fromperipheralblood	blood
49	chr2:113878800-113879400	Enhancers	Primary B cells from cord blood	blood
50	chr2:113878800-113879600	Enhancers	NHEK	skin

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