Variant report

Variant	nsv874878
Chromosome Location	chr2:113742734-113776076
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:203)
CpG islands
(count:429)
Chromatin interactive
region (count:26)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:203 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:113757999-113758367	K562	blood:	n/a	n/a
2	ARID3A	chr2:113770058-113771640	K562	blood:	n/a	n/a
3	ARID3A	chr2:113758171-113758234	HepG2	liver:	n/a	n/a
4	ATF1	chr2:113767753-113767985	K562	blood:	n/a	n/a
5	ATF1	chr2:113770285-113770787	K562	blood:	n/a	n/a
6	ATF3	chr2:113770356-113771033	K562	blood:	n/a	n/a
7	ATF3	chr2:113770355-113770988	A549	lung:	n/a	n/a
8	BACH1	chr2:113768044-113768063	K562	blood:	n/a	n/a
9	BACH1	chr2:113770155-113770865	K562	blood:	n/a	n/a
10	BCL3	chr2:113770223-113770834	A549	lung:	n/a	n/a
11	BHLHE40	chr2:113770380-113770835	K562	blood:	n/a	n/a
12	CBX3	chr2:113758069-113758425	HCT-116	colon:	n/a	n/a
13	CBX3	chr2:113757942-113758593	K562	blood:	n/a	n/a
14	CBX3	chr2:113770089-113770990	K562	blood:	n/a	n/a
15	CBX3	chr2:113770035-113770964	K562	blood:	n/a	n/a
16	CBX3	chr2:113757844-113758512	K562	blood:	n/a	n/a
17	CCNT2	chr2:113770168-113770866	K562	blood:	n/a	n/a
18	CEBPB	chr2:113770326-113770843	K562	blood:	n/a	n/a
19	CEBPB	chr2:113751417-113751679	HepG2	liver:	n/a	n/a
20	CEBPB	chr2:113770299-113770917	K562	blood:	n/a	n/a
21	CEBPB	chr2:113770342-113770783	A549	lung:	n/a	n/a
22	CEBPD	chr2:113770222-113770940	K562	blood:	n/a	n/a
23	CEBPD	chr2:113770220-113770955	K562	blood:	n/a	n/a
24	CHD2	chr2:113770416-113770775	K562	blood:	n/a	n/a
25	CREB1	chr2:113770137-113770921	K562	blood:	n/a	n/a
26	CREB1	chr2:113751409-113751865	HepG2	liver:	n/a	n/a
27	CREB1	chr2:113751411-113751890	HepG2	liver:	n/a	n/a
28	CTCF	chr2:113750595-113750649	K562	blood:	n/a	n/a
29	CTCF	chr2:113750700-113750850	HepG2	liver:	n/a	n/a
30	CTCF	chr2:113750620-113750770	WERI-Rb-1	eye:	n/a	n/a
31	CTCF	chr2:113742508-113742803	K562	blood:	n/a	n/a
32	CUX1	chr2:113774702-113774966	K562	blood:	n/a	n/a
33	CUX1	chr2:113770106-113770828	K562	blood:	n/a	n/a
34	CUX1	chr2:113747215-113747499	K562	blood:	n/a	n/a
35	E2F6	chr2:113753033-113753149	K562	blood:	n/a	n/a
36	ELF1	chr2:113754229-113754637	GM12878	blood:	n/a	n/a
37	EP300	chr2:113770499-113770873	GM12878	blood:	n/a	n/a
38	EP300	chr2:113767735-113768025	K562	blood:	n/a	n/a
39	EP300	chr2:113775913-113775938	K562	blood:	n/a	n/a
40	EP300	chr2:113769419-113769663	K562	blood:	n/a	n/a
41	EP300	chr2:113770129-113771307	K562	blood:	n/a	n/a
42	EP300	chr2:113770394-113770766	K562	blood:	n/a	n/a
43	EP300	chr2:113770176-113770987	A549	lung:	n/a	n/a
44	EP300	chr2:113770020-113770051	GM12878	blood:	n/a	n/a
45	EP300	chr2:113770281-113770858	A549	lung:	n/a	n/a
46	EP300	chr2:113758083-113758352	K562	blood:	n/a	n/a
47	FOS	chr2:113770594-113770704	MCF10A-Er-Src	breast:	n/a	n/a
48	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
49	FOS	chr2:113770447-113770846	K562	blood:	n/a	n/a
50	FOS	chr2:113770512-113770704	MCF10A-Er-Src	breast:	n/a	n/a

(count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:113742967-113743017	AG10803	skin:	n/a
2	chr2:113762280-113762330	Jurkat	blood:	n/a
3	chr2:113742967-113743017	AG10803	skin:	n/a
4	chr2:113762280-113762330	Jurkat	blood:	n/a
5	chr2:113763093-113763143	HRPEpiC	eye:	n/a
6	chr2:113763093-113763143	HAEpiC	amniotic membrane:	n/a
7	chr2:113763326-113763376	HPAEpiC	pulmonary alveolar:	n/a
8	chr2:113763906-113763956	AG09309	skin:	n/a
9	chr2:113762795-113762845	HEK293	kidney:	embryo
10	chr2:113762280-113762330	AG09319	gingival:	n/a
11	chr2:113742967-113743017	MCF-7	breast:	n/a
12	chr2:113763906-113763956	GM12892	blood:	n/a
13	chr2:113763326-113763376	GM12891	blood:	n/a
14	chr2:113763326-113763376	SAEC	small airway:	n/a
15	chr2:113763326-113763376	NH-A	brain:	n/a
16	chr2:113763393-113763443	HIPEpiC	eye:	n/a
17	chr2:113763093-113763143	GM19239	blood:	n/a
18	chr2:113762795-113762845	SK-N-SH_RA	brain:	n/a
19	chr2:113762280-113762330	NT2-D1	testis:	n/a
20	chr2:113763393-113763443	RPTEC	kidney:	n/a
21	chr2:113763093-113763143	H1-hESC	embryonic stem cell:	embryo
22	chr2:113762795-113762845	Jurkat	blood:	n/a
23	chr2:113763906-113763956	HEK293	kidney:	embryo
24	chr2:113763906-113763956	AG04449	skin:	fetal
25	chr2:113762280-113762330	K562	blood:	n/a
26	chr2:113762280-113762330	GM12892	blood:	n/a
27	chr2:113763093-113763143	HL-60	blood:	n/a
28	chr2:113763093-113763143	HPAEpiC	pulmonary alveolar:	n/a
29	chr2:113742967-113743017	GM19239	blood:	n/a
30	chr2:113763906-113763956	Hela-S3	cervix:	n/a
31	chr2:113763906-113763956	PrEC	prostate:	n/a
32	chr2:113763326-113763376	HMEC	breast:	n/a
33	chr2:113763093-113763143	NT2-D1	testis:	n/a
34	chr2:113762795-113762845	GM12892	blood:	n/a
35	chr2:113762795-113762845	ECC-1	luminal epithelium:	n/a
36	chr2:113762280-113762330	HEEpiC	esophagus:	n/a
37	chr2:113763093-113763143	SK-N-MC	brain:	n/a
38	chr2:113763393-113763443	HMEC	breast:	n/a
39	chr2:113762795-113762845	NHDF-neo	bronchial:	n/a
40	chr2:113763093-113763143	ECC-1	luminal epithelium:	n/a
41	chr2:113763326-113763376	HRPEpiC	eye:	n/a
42	chr2:113763326-113763376	H1-hESC	embryonic stem cell:	embryo
43	chr2:113763093-113763143	BJ	skin:	n/a
44	chr2:113742967-113743017	NB4	blood:	n/a
45	chr2:113763906-113763956	K562	blood:	n/a
46	chr2:113762280-113762330	HNPCEpiC	eye:	n/a
47	chr2:113763393-113763443	AG09319	gingival:	n/a
48	chr2:113763393-113763443	HEEpiC	esophagus:	n/a
49	chr2:113763393-113763443	U87	brain:	n/a
50	chr2:113763326-113763376	PFSK-1	brain:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:113751007..113754364-chr2:113757829..113763549,5	K562	blood:
2	chr2:113764595..113766525-chr2:113767094..113769506,2	K562	blood:
3	chr2:113753961..113756170-chr2:113760057..113761673,2	MCF-7	breast:
4	chr2:113756642..113760265-chr2:113761535..113765046,5	K562	blood:
5	chr2:113756435..113758227-chr2:113770315..113771981,2	K562	blood:
6	chr2:113765610..113767817-chr2:113769200..113772024,4	K562	blood:
7	chr2:113768707..113772207-chr2:113772751..113775961,3	K562	blood:
8	chr2:113768707..113772207-chr2:113772751..113775961,3	K562	blood:
9	chr2:113760067..113761681-chr2:113763632..113765728,2	K562	blood:
10	chr2:113741054..113743691-chr2:113744303..113746180,2	K562	blood:
11	chr2:113751007..113754364-chr2:113757829..113763549,5	K562	blood:
12	chr2:113757048..113759917-chr2:113761667..113764022,3	MCF-7	breast:
13	chr2:113760067..113761681-chr2:113763632..113765728,2	K562	blood:
14	chr2:113757191..113759734-chr2:113762497..113764783,2	K562	blood:
15	chr2:113772280..113775208-chr2:113776344..113777930,2	K562	blood:
16	chr2:113756681..113759563-chr2:113795115..113796939,2	K562	blood:
17	chr2:113692325..113694742-chr2:113763398..113765744,2	K562	blood:
18	chr2:113751007..113752612-chr2:113760021..113762623,2	K562	blood:
19	chr2:113741483..113743922-chr2:113839528..113841138,2	K562	blood:
20	chr2:113756435..113758227-chr2:113770315..113771981,2	K562	blood:
21	chr2:113764595..113766525-chr2:113767094..113769506,2	K562	blood:
22	chr2:113741054..113743691-chr2:113744303..113746180,2	K562	blood:
23	chr2:113751007..113752612-chr2:113760021..113762623,2	K562	blood:
24	chr2:113753961..113756170-chr2:113760057..113761673,2	MCF-7	breast:
25	chr2:113752348..113754639-chr2:113757517..113759380,2	MCF-7	breast:
26	chr2:113765610..113767817-chr2:113769200..113772024,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IL36A-1	chr2:113753094-113753514	NONHSAT073738

No data

Variant related genes	Relation type
IL36A	TF binding region
ENSG00000232090	TF binding region
HMGN2P23	TF binding region
IL36A	CpG island
ENSG00000232090	CpG island
HMGN2P23	CpG island
ENSG00000232090	chromatin interactions
ENSG00000136694	chromatin interactions

Extended variants
information (count: 1143 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:1143 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7584409	chr2:113742734-113742735	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs75448924	chr2:113742746-113742747	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs77810983	chr2:113742843-113742844	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs556348420	chr2:113742959-113742960	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs576182352	chr2:113742966-113742967	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs116028383	chr2:113743091-113743092	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs200838854	chr2:113743109-113743110	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs571915555	chr2:113743154-113743155	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs558998968	chr2:113743155-113743156	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs572380413	chr2:113743195-113743196	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs541390889	chr2:113743232-113743233	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561236139	chr2:113743242-113743243	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs182139707	chr2:113743297-113743298	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs34066489	chr2:113743347-113743348	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs564781975	chr2:113743350-113743351	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs80189220	chr2:113743352-113743353	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs531531579	chr2:113743377-113743378	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs186820765	chr2:113743452-113743453	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs551229092	chr2:113743456-113743457	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs571305273	chr2:113743458-113743459	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs527317247	chr2:113743572-113743573	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs28954070	chr2:113743573-113743574	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs140692572	chr2:113743588-113743589	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs191618119	chr2:113743691-113743692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs182828012	chr2:113743733-113743734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs569954424	chr2:113743740-113743741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs373065564	chr2:113743754-113743755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs150458721	chr2:113743762-113743763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs572522130	chr2:113743778-113743779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs534778097	chr2:113743808-113743809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs138266414	chr2:113743813-113743814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs531372572	chr2:113743869-113743870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs574840711	chr2:113743938-113743939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs28954071	chr2:113743970-113743971	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs557498756	chr2:113744013-113744014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs28954072	chr2:113744015-113744016	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs577665931	chr2:113744035-113744036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs74355704	chr2:113744156-113744157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs143277454	chr2:113744167-113744168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs545166534	chr2:113744168-113744169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs28954073	chr2:113744319-113744320	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs5833477	chr2:113744383-113744384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs116364298	chr2:113744413-113744414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs547042310	chr2:113744470-113744471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs560595583	chr2:113744498-113744499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs529630993	chr2:113744624-113744625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs550094341	chr2:113744666-113744667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs188610842	chr2:113744678-113744679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs538932882	chr2:113744769-113744770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552751072	chr2:113744883-113744884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD

Chromatin state (count:149 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:113736000-113747400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:113742000-113743800	Enhancers	Primary T killer memory cells from peripheral blood	blood
3	chr2:113742000-113744000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
4	chr2:113742200-113743800	Enhancers	Fetal Thymus	thymus
5	chr2:113742200-113744000	Enhancers	Primary T helper naive cells from peripheral blood	blood
6	chr2:113742200-113744000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
7	chr2:113742200-113744000	Enhancers	Primary T helper cells fromperipheralblood	blood
8	chr2:113742200-113744200	Enhancers	Primary T cells from cord blood	blood
9	chr2:113742400-113743600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr2:113742400-113743600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
11	chr2:113742400-113743800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
12	chr2:113742400-113744000	Enhancers	Primary T cells fromperipheralblood	blood
13	chr2:113742400-113744000	Enhancers	Primary T helper cells PMA-I stimulated	--
14	chr2:113742400-113744200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
15	chr2:113742600-113743200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
16	chr2:113742600-113743800	Enhancers	Thymus	Thymus
17	chr2:113742600-113744000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
18	chr2:113747400-113747600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr2:113747600-113747800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr2:113750600-113750800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
21	chr2:113750600-113751000	Enhancers	Primary T cells fromperipheralblood	blood
22	chr2:113750600-113754400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
23	chr2:113750800-113751200	Weak transcription	Liver	Liver
24	chr2:113750800-113751400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
25	chr2:113751000-113752000	Weak transcription	Primary T cells fromperipheralblood	blood
26	chr2:113751200-113752200	Enhancers	HepG2	liver
27	chr2:113751200-113753200	Enhancers	Primary T helper naive cells from peripheral blood	blood
28	chr2:113751200-113755600	Enhancers	Primary T helper cells fromperipheralblood	blood
29	chr2:113751400-113752000	Enhancers	Liver	Liver
30	chr2:113751400-113753000	Enhancers	Primary T helper cells PMA-I stimulated	--
31	chr2:113751400-113755600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
32	chr2:113751600-113753200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
33	chr2:113751800-113752400	Enhancers	Stomach Mucosa	stomach
34	chr2:113751800-113755600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
35	chr2:113752000-113753200	Enhancers	Primary T killer memory cells from peripheral blood	blood
36	chr2:113752000-113754400	Enhancers	Primary T cells from cord blood	blood
37	chr2:113752000-113755600	Enhancers	Primary T cells fromperipheralblood	blood
38	chr2:113752200-113753000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
39	chr2:113752400-113753000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr2:113752800-113753000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
41	chr2:113753000-113753200	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
42	chr2:113753000-113753200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
43	chr2:113753000-113753200	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr2:113753000-113753400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
45	chr2:113753000-113753800	Enhancers	K562	blood
46	chr2:113753000-113754400	Enhancers	Fetal Thymus	thymus
47	chr2:113753000-113755200	Enhancers	Dnd41	blood
48	chr2:113753200-113753400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
49	chr2:113753200-113753400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
50	chr2:113753200-113753400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links