Variant report

Variant	nsv963895
Chromosome Location	chr2:113760993-113772508
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:131)
CpG islands
(count:366)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:131 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:113770058-113771640	K562	blood:	n/a	n/a
2	ATF1	chr2:113767753-113767985	K562	blood:	n/a	n/a
3	ATF1	chr2:113770285-113770787	K562	blood:	n/a	n/a
4	ATF3	chr2:113770355-113770988	A549	lung:	n/a	n/a
5	ATF3	chr2:113770356-113771033	K562	blood:	n/a	n/a
6	BACH1	chr2:113770155-113770865	K562	blood:	n/a	n/a
7	BACH1	chr2:113768044-113768063	K562	blood:	n/a	n/a
8	BCL3	chr2:113770223-113770834	A549	lung:	n/a	n/a
9	BHLHE40	chr2:113770380-113770835	K562	blood:	n/a	n/a
10	CBX3	chr2:113770089-113770990	K562	blood:	n/a	n/a
11	CBX3	chr2:113770035-113770964	K562	blood:	n/a	n/a
12	CCNT2	chr2:113770168-113770866	K562	blood:	n/a	n/a
13	CEBPB	chr2:113770326-113770843	K562	blood:	n/a	n/a
14	CEBPB	chr2:113770299-113770917	K562	blood:	n/a	n/a
15	CEBPB	chr2:113770342-113770783	A549	lung:	n/a	n/a
16	CEBPD	chr2:113770222-113770940	K562	blood:	n/a	n/a
17	CEBPD	chr2:113770220-113770955	K562	blood:	n/a	n/a
18	CHD2	chr2:113770416-113770775	K562	blood:	n/a	n/a
19	CREB1	chr2:113770137-113770921	K562	blood:	n/a	n/a
20	CUX1	chr2:113770106-113770828	K562	blood:	n/a	n/a
21	EP300	chr2:113770281-113770858	A549	lung:	n/a	n/a
22	EP300	chr2:113770176-113770987	A549	lung:	n/a	n/a
23	EP300	chr2:113770020-113770051	GM12878	blood:	n/a	n/a
24	EP300	chr2:113770499-113770873	GM12878	blood:	n/a	n/a
25	EP300	chr2:113767735-113768025	K562	blood:	n/a	n/a
26	EP300	chr2:113770129-113771307	K562	blood:	n/a	n/a
27	EP300	chr2:113770394-113770766	K562	blood:	n/a	n/a
28	EP300	chr2:113769419-113769663	K562	blood:	n/a	n/a
29	FOS	chr2:113762730-113762822	MCF10A-Er-Src	breast:	n/a	chr2:113762769-113762777 chr2:113762770-113762777 chr2:113762769-113762778 chr2:113762767-113762779 chr2:113762768-113762777
30	FOS	chr2:113762640-113762863	MCF10A-Er-Src	breast:	n/a	chr2:113762769-113762777 chr2:113762770-113762777 chr2:113762769-113762778 chr2:113762767-113762779 chr2:113762768-113762777
31	FOS	chr2:113770594-113770704	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr2:113770512-113770704	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr2:113762740-113762896	MCF10A-Er-Src	breast:	n/a	chr2:113762769-113762777 chr2:113762770-113762777 chr2:113762769-113762778 chr2:113762767-113762779 chr2:113762768-113762777
34	FOS	chr2:113770447-113770846	K562	blood:	n/a	n/a
35	FOSL1	chr2:113770346-113770864	K562	blood:	n/a	n/a
36	FOSL1	chr2:113770431-113770761	K562	blood:	n/a	n/a
37	FOSL2	chr2:113770386-113770821	A549	lung:	n/a	n/a
38	FOSL2	chr2:113770254-113771011	A549	lung:	n/a	n/a
39	FOXA2	chr2:113770284-113770920	A549	lung:	n/a	n/a
40	FOXA2	chr2:113770271-113770836	A549	lung:	n/a	n/a
41	GATA1	chr2:113770188-113771201	PBDE	blood:	n/a	n/a
42	GATA1	chr2:113769993-113771987	K562	blood:	n/a	n/a
43	GATA2	chr2:113770278-113770874	K562	blood:	n/a	n/a
44	GATA2	chr2:113770265-113770906	K562	blood:	n/a	n/a
45	GATA2	chr2:113770351-113770832	K562	blood:	n/a	n/a
46	GATA3	chr2:113770289-113770859	MCF-7	breast:	n/a	chr2:113770569-113770577
47	GATA3	chr2:113767689-113768111	SK-N-SH	brain:	n/a	n/a
48	GATA3	chr2:113770289-113770768	A549	lung:	n/a	chr2:113770569-113770577
49	GATA3	chr2:113770122-113770883	A549	lung:	n/a	chr2:113770569-113770577
50	GATA3	chr2:113767655-113768105	SK-N-SH	brain:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:113762795-113762845	HCPEpiC	choroid plexus:	n/a
2	chr2:113763906-113763956	NHBE	bronchial:	n/a
3	chr2:113762795-113762845	PANC-1	pancreas:	n/a
4	chr2:113763093-113763143	AG09319	gingival:	n/a
5	chr2:113763906-113763956	HCT-116	colon:	n/a
6	chr2:113762795-113762845	GM06990	blood:	n/a
7	chr2:113763326-113763376	SK-N-SH_RA	brain:	n/a
8	chr2:113763906-113763956	CMK	blood:	n/a
9	chr2:113763093-113763143	HNPCEpiC	eye:	n/a
10	chr2:113763093-113763143	H1-hESC	embryonic stem cell:	embryo
11	chr2:113762795-113762845	K562	blood:	n/a
12	chr2:113763326-113763376	SAEC	small airway:	n/a
13	chr2:113763093-113763143	SK-N-SH_RA	brain:	n/a
14	chr2:113763326-113763376	MCF10A-Er-Src	breast:	n/a
15	chr2:113763326-113763376	NHDF-neo	bronchial:	n/a
16	chr2:113762795-113762845	SKMC	muscle:	n/a
17	chr2:113763326-113763376	HIPEpiC	eye:	n/a
18	chr2:113763906-113763956	Jurkat	blood:	n/a
19	chr2:113762280-113762330	HAEpiC	amniotic membrane:	n/a
20	chr2:113763393-113763443	T-47D	breast:	n/a
21	chr2:113763093-113763143	GM12891	blood:	n/a
22	chr2:113763393-113763443	ProgFib	skin:	n/a
23	chr2:113763393-113763443	HRE	kidney:	n/a
24	chr2:113762795-113762845	GM12892	blood:	n/a
25	chr2:113762795-113762845	HRPEpiC	eye:	n/a
26	chr2:113763906-113763956	MCF10A-Er-Src	breast:	n/a
27	chr2:113762280-113762330	SAEC	small airway:	n/a
28	chr2:113763393-113763443	HL-60	blood:	n/a
29	chr2:113763326-113763376	AG04449	skin:	fetal
30	chr2:113763093-113763143	HEK293	kidney:	embryo
31	chr2:113762280-113762330	HMEC	breast:	n/a
32	chr2:113763906-113763956	BE2_C	brain:	n/a
33	chr2:113763906-113763956	HIPEpiC	eye:	n/a
34	chr2:113762795-113762845	NT2-D1	testis:	n/a
35	chr2:113763326-113763376	MCF-7	breast:	n/a
36	chr2:113763326-113763376	HRCEpiC	kidney:	n/a
37	chr2:113762795-113762845	CMK	blood:	n/a
38	chr2:113762795-113762845	BE2_C	brain:	n/a
39	chr2:113763326-113763376	BE2_C	brain:	n/a
40	chr2:113763326-113763376	NH-A	brain:	n/a
41	chr2:113763326-113763376	GM19239	blood:	n/a
42	chr2:113763326-113763376	HAEpiC	amniotic membrane:	n/a
43	chr2:113763093-113763143	HCM	heart:	n/a
44	chr2:113763906-113763956	AG09309	skin:	n/a
45	chr2:113763906-113763956	HAEpiC	amniotic membrane:	n/a
46	chr2:113763093-113763143	LNCaP	prostate:	n/a
47	chr2:113762795-113762845	ECC-1	luminal epithelium:	n/a
48	chr2:113763093-113763143	Hepatocyte	liver:	n/a
49	chr2:113762795-113762845	HepG2	liver:	n/a
50	chr2:113763393-113763443	MCF10A-Er-Src	breast:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:113765610..113767817-chr2:113769200..113772024,4	K562	blood:
2	chr2:113764595..113766525-chr2:113767094..113769506,2	K562	blood:
3	chr2:113692325..113694742-chr2:113763398..113765744,2	K562	blood:
4	chr2:113760067..113761681-chr2:113763632..113765728,2	K562	blood:
5	chr2:113765610..113767817-chr2:113769200..113772024,4	K562	blood:
6	chr2:113751007..113754364-chr2:113757829..113763549,5	K562	blood:
7	chr2:113764595..113766525-chr2:113767094..113769506,2	K562	blood:
8	chr2:113760067..113761681-chr2:113763632..113765728,2	K562	blood:
9	chr2:113756435..113758227-chr2:113770315..113771981,2	K562	blood:
10	chr2:113753961..113756170-chr2:113760057..113761673,2	MCF-7	breast:
11	chr2:113772280..113775208-chr2:113776344..113777930,2	K562	blood:
12	chr2:113751007..113752612-chr2:113760021..113762623,2	K562	blood:
13	chr2:113768707..113772207-chr2:113772751..113775961,3	K562	blood:

No data

Variant related genes	Relation type
IL36A	TF binding region
IL36A	CpG island
ENSG00000232090	chromatin interactions

Extended variants
information (count: 431 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:431 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185851129	chr2:113761027-113761028	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs368850901	chr2:113761071-113761072	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs190653137	chr2:113761084-113761085	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs1026023	chr2:113761085-113761086	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs569627729	chr2:113761090-113761091	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs1026022	chr2:113761104-113761105	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs551953605	chr2:113761130-113761131	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs565863491	chr2:113761146-113761147	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs79031289	chr2:113761150-113761151	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs28938795	chr2:113761159-113761160	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs77049789	chr2:113761177-113761178	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs537067362	chr2:113761179-113761180	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs531332229	chr2:113761187-113761188	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs377678837	chr2:113761194-113761195	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs556963433	chr2:113761212-113761213	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs577621659	chr2:113761215-113761216	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs548494515	chr2:113761298-113761299	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs144990659	chr2:113761312-113761313	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs28993968	chr2:113761316-113761317	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs546472778	chr2:113761335-113761336	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs28938796	chr2:113761342-113761343	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs573379133	chr2:113761398-113761399	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs6732775	chr2:113761428-113761429	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs147699809	chr2:113761452-113761453	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs1020404	chr2:113761473-113761474	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs544206626	chr2:113761509-113761510	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs371229665	chr2:113761544-113761545	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs532319715	chr2:113761583-113761584	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs552986134	chr2:113761605-113761606	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs534185441	chr2:113761687-113761688	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs548069666	chr2:113761790-113761791	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs149152676	chr2:113761808-113761809	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs142278259	chr2:113761832-113761833	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs540840344	chr2:113761857-113761858	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs183800735	chr2:113761860-113761861	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs187577526	chr2:113761882-113761883	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs13382878	chr2:113761931-113761932	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs537102050	chr2:113762135-113762136	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs556999676	chr2:113762150-113762151	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs192026145	chr2:113762152-113762153	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs540178760	chr2:113762160-113762161	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs553615554	chr2:113762188-113762189	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs573387837	chr2:113762219-113762220	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs28993969	chr2:113762224-113762225	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs555638060	chr2:113762269-113762270	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs12620293	chr2:113762279-113762280	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs573117987	chr2:113762280-113762281	Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs559105399	chr2:113762281-113762282	Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs28938797	chr2:113762292-113762293	Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs72827826	chr2:113762295-113762296	Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

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	17483303	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
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Ocular motor apraxia	21572526	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Idiopathic chronic pancreatitis	21549014	CNVD
Mental retardation	21549014	CNVD
Maculopathy	20981449	CNVD
Nephronophthisis	22470819	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
Acute lymphoblastic leukemia	18458336	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	17699850	CNVD
Ovarian cancer	17699850	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:113759200-113765000	Weak transcription	Primary T cells from cord blood	blood
2	chr2:113763200-113764400	Active TSS	Esophagus	oesophagus
3	chr2:113763600-113763800	Enhancers	Gastric	stomach
4	chr2:113764400-113766800	Weak transcription	Esophagus	oesophagus
5	chr2:113764800-113765600	Active TSS	Gastric	stomach
6	chr2:113765000-113765600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
7	chr2:113765000-113765800	Enhancers	Primary T cells from cord blood	blood
8	chr2:113765200-113765800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
9	chr2:113765400-113765800	Enhancers	Fetal Thymus	thymus
10	chr2:113765600-113773000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr2:113765600-113797400	Weak transcription	Gastric	stomach
12	chr2:113765800-113767200	Weak transcription	Primary T cells from cord blood	blood
13	chr2:113765800-113767200	Weak transcription	Fetal Thymus	thymus
14	chr2:113765800-113773000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr2:113767000-113768000	Enhancers	Thymus	Thymus
16	chr2:113767200-113767400	Enhancers	Primary T cells from cord blood	blood
17	chr2:113767200-113767400	Enhancers	A549	lung
18	chr2:113767200-113768200	Enhancers	Fetal Thymus	thymus
19	chr2:113767200-113768600	Enhancers	Placenta Amnion	Placenta Amnion
20	chr2:113767400-113768000	Weak transcription	Primary T cells from cord blood	blood
21	chr2:113767400-113770200	Weak transcription	A549	lung
22	chr2:113767600-113767800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr2:113767600-113768200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr2:113767600-113768200	Enhancers	HMEC	breast
25	chr2:113767600-113770400	Enhancers	K562	blood
26	chr2:113767800-113768200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr2:113767800-113768200	Enhancers	Osteobl	bone
28	chr2:113768000-113768200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr2:113768000-113768800	Enhancers	Primary T cells from cord blood	blood
30	chr2:113768000-113769200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr2:113768200-113770000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr2:113768200-113770200	Weak transcription	Osteobl	bone
33	chr2:113768200-113770400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr2:113768200-113773400	Weak transcription	Fetal Thymus	thymus
35	chr2:113768800-113771400	Weak transcription	Primary T cells from cord blood	blood
36	chr2:113769200-113771400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr2:113770000-113771000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr2:113770000-113771200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr2:113770200-113770600	Flanking Active TSS	A549	lung
40	chr2:113770200-113770600	Enhancers	Osteobl	bone
41	chr2:113770200-113771000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr2:113770200-113771000	Enhancers	Stomach Mucosa	stomach
43	chr2:113770400-113770800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr2:113770400-113770800	Flanking Active TSS	K562	blood
45	chr2:113770400-113771200	Enhancers	NHEK	skin
46	chr2:113770600-113771800	Enhancers	A549	lung
47	chr2:113770800-113771200	Active TSS	K562	blood
48	chr2:113771200-113771400	Flanking Active TSS	K562	blood
49	chr2:113771400-113772000	Enhancers	K562	blood
50	chr2:113771400-113773800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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