Variant report

Variant	nsv999789
Chromosome Location	chr2:36355625-36549716
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:36392370-36392619	HepG2	liver:	n/a	n/a
2	ATF2	chr2:36374728-36375202	GM12878	blood:	n/a	n/a
3	ATF2	chr2:36473245-36473881	GM12878	blood:	n/a	n/a
4	ATF2	chr2:36497853-36498342	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr2:36473354-36473889	GM12878	blood:	n/a	n/a
6	BACH1	chr2:36545626-36545719	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr2:36417402-36417520	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr2:36473528-36473788	GM12878	blood:	n/a	n/a
9	BATF	chr2:36474136-36474343	GM12878	blood:	n/a	chr2:36474255-36474266
10	BATF	chr2:36467483-36467862	GM12878	blood:	n/a	n/a
11	BATF	chr2:36374889-36375165	GM12878	blood:	n/a	n/a
12	BATF	chr2:36374886-36375226	GM12878	blood:	n/a	n/a
13	BCL11A	chr2:36374942-36375184	GM12878	blood:	n/a	chr2:36374970-36374979
14	BCL11A	chr2:36497933-36498242	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCL11A	chr2:36506762-36507002	H1-hESC	embryonic stem cell:	n/a	n/a
16	BCL11A	chr2:36473409-36473790	GM12878	blood:	n/a	chr2:36473585-36473594
17	BCL3	chr2:36473447-36473808	GM12878	blood:	n/a	chr2:36473585-36473594
18	BCLAF1	chr2:36467548-36468268	GM12878	blood:	n/a	n/a
19	BCLAF1	chr2:36473380-36473879	GM12878	blood:	n/a	chr2:36473585-36473594
20	BHLHE40	chr2:36411001-36411307	HepG2	liver:	n/a	n/a
21	BRCA1	chr2:36473771-36473792	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr2:36546010-36546093	HepG2	liver:	n/a	n/a
23	CEBPB	chr2:36434759-36434959	IMR90	lung:	n/a	chr2:36434830-36434841
24	CEBPB	chr2:36449701-36449936	K562	blood:	n/a	chr2:36449811-36449820 chr2:36449811-36449820 chr2:36449810-36449821 chr2:36449809-36449822 chr2:36449811-36449820 chr2:36449809-36449822
25	CEBPB	chr2:36473340-36473968	GM12878	blood:	n/a	n/a
26	CEBPB	chr2:36436903-36436987	HepG2	liver:	n/a	n/a
27	CEBPB	chr2:36395338-36395598	Hela-S3	cervix:	n/a	chr2:36395482-36395495 chr2:36395482-36395493 chr2:36395482-36395495 chr2:36395484-36395495 chr2:36395479-36395496
28	CEBPB	chr2:36514655-36514886	H1-hESC	embryonic stem cell:	n/a	chr2:36514780-36514791
29	CEBPB	chr2:36449673-36449993	H1-hESC	embryonic stem cell:	n/a	chr2:36449811-36449820 chr2:36449811-36449820 chr2:36449810-36449821 chr2:36449809-36449822 chr2:36449811-36449820 chr2:36449809-36449822
30	CEBPB	chr2:36420124-36420491	ECC-1	luminal epithelium:	n/a	chr2:36420312-36420325
31	CEBPB	chr2:36506728-36507022	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr2:36395475-36395510	IMR90	lung:	n/a	chr2:36395482-36395495 chr2:36395482-36395493 chr2:36395482-36395495 chr2:36395484-36395495 chr2:36395479-36395496
33	CEBPB	chr2:36374848-36374960	HepG2	liver:	n/a	chr2:36374901-36374912 chr2:36374900-36374911
34	CEBPB	chr2:36380814-36381038	IMR90	lung:	n/a	chr2:36380974-36380985
35	CEBPB	chr2:36375217-36375486	HepG2	liver:	n/a	n/a
36	CEBPB	chr2:36379312-36379579	HepG2	liver:	n/a	chr2:36379457-36379468
37	CEBPB	chr2:36437519-36437741	A549	lung:	n/a	chr2:36437627-36437638
38	CEBPB	chr2:36420172-36420519	ECC-1	luminal epithelium:	n/a	chr2:36420312-36420325
39	CEBPB	chr2:36449665-36449982	A549	lung:	n/a	chr2:36449811-36449820 chr2:36449811-36449820 chr2:36449810-36449821 chr2:36449809-36449822 chr2:36449811-36449820 chr2:36449809-36449822
40	CEBPB	chr2:36521592-36521787	A549	lung:	n/a	n/a
41	CEBPB	chr2:36395379-36395613	A549	lung:	n/a	chr2:36395482-36395495 chr2:36395482-36395493 chr2:36395482-36395495 chr2:36395484-36395495 chr2:36395479-36395496
42	CEBPB	chr2:36375197-36375400	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr2:36549402-36549551	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr2:36374793-36375473	Hela-S3	cervix:	n/a	chr2:36374901-36374912 chr2:36374900-36374911
45	CEBPB	chr2:36375180-36375486	A549	lung:	n/a	n/a
46	CEBPB	chr2:36437530-36437813	HepG2	liver:	n/a	chr2:36437627-36437638
47	CEBPB	chr2:36434705-36434959	A549	lung:	n/a	chr2:36434830-36434841
48	CEBPB	chr2:36419090-36419285	HepG2	liver:	n/a	n/a
49	CEBPB	chr2:36514534-36514969	IMR90	lung:	n/a	chr2:36514780-36514791
50	CEBPB	chr2:36548842-36549024	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:36441749-36441799	T-47D	breast:	n/a
2	chr2:36467699-36467749	ovcar-3	ovarian:	n/a
3	chr2:36467699-36467749	PFSK-1	brain:	n/a
4	chr2:36441749-36441799	SK-N-SH	brain:	n/a
5	chr2:36467699-36467749	GM12891	blood:	n/a
6	chr2:36467699-36467749	NT2-D1	testis:	n/a
7	chr2:36406592-36406642	HCPEpiC	choroid plexus:	n/a
8	chr2:36467699-36467749	HNPCEpiC	eye:	n/a
9	chr2:36467699-36467749	SK-N-MC	brain:	n/a
10	chr2:36406592-36406642	PFSK-1	brain:	n/a
11	chr2:36467699-36467749	HepG2	liver:	n/a
12	chr2:36406592-36406642	NT2-D1	testis:	n/a
13	chr2:36406592-36406642	IMR90	lung:	fetal
14	chr2:36406592-36406642	PANC-1	pancreas:	n/a
15	chr2:36467699-36467749	HEEpiC	esophagus:	n/a
16	chr2:36441749-36441799	HepG2	liver:	n/a
17	chr2:36406592-36406642	BE2_C	brain:	n/a
18	chr2:36441749-36441799	A549	lung:	n/a
19	chr2:36441749-36441799	SK-N-SH_RA	brain:	n/a
20	chr2:36441749-36441799	HRCEpiC	kidney:	n/a
21	chr2:36467699-36467749	HPAEpiC	pulmonary alveolar:	n/a
22	chr2:36467699-36467749	HRE	kidney:	n/a
23	chr2:36467699-36467749	HIPEpiC	eye:	n/a
24	chr2:36406592-36406642	NH-A	brain:	n/a
25	chr2:36441749-36441799	HRE	kidney:	n/a
26	chr2:36441749-36441799	NHDF-neo	bronchial:	n/a
27	chr2:36441749-36441799	CMK	blood:	n/a
28	chr2:36467699-36467749	GM06990	blood:	n/a
29	chr2:36467699-36467749	Hela-S3	cervix:	n/a
30	chr2:36467699-36467749	GM12878	blood:	n/a
31	chr2:36406592-36406642	GM12878	blood:	n/a
32	chr2:36406592-36406642	SAEC	small airway:	n/a
33	chr2:36467699-36467749	NB4	blood:	n/a
34	chr2:36406592-36406642	GM12892	blood:	n/a
35	chr2:36406592-36406642	T-47D	breast:	n/a
36	chr2:36467699-36467749	IMR90	lung:	fetal
37	chr2:36406592-36406642	GM06990	blood:	n/a
38	chr2:36467699-36467749	AG04450	lung:	fetal
39	chr2:36406592-36406642	RPTEC	kidney:	n/a
40	chr2:36467699-36467749	CMK	blood:	n/a
41	chr2:36406592-36406642	Hela-S3	cervix:	n/a
42	chr2:36441749-36441799	Caco-2	colon:	n/a
43	chr2:36441749-36441799	SAEC	small airway:	n/a
44	chr2:36467699-36467749	SAEC	small airway:	n/a
45	chr2:36467699-36467749	SK-N-SH_RA	brain:	n/a
46	chr2:36441749-36441799	SKMC	muscle:	n/a
47	chr2:36467699-36467749	SKMC	muscle:	n/a
48	chr2:36406592-36406642	HEEpiC	esophagus:	n/a
49	chr2:36467699-36467749	HL-60	blood:	n/a
50	chr2:36467699-36467749	AG04449	skin:	fetal

No.	Distal block	Cell Line	Cell type
1	chr2:36375898..36378508-chr2:36382841..36384658,2	K562	blood:
2	chr2:36511790..36513367-chr2:36515871..36517386,2	MCF-7	breast:
3	chr2:36511790..36513367-chr2:36515871..36517386,2	MCF-7	breast:
4	chr2:36198079..36198752-chr2:36549195..36549978,3	MCF-7	breast:
5	chr2:36426823..36429485-chr2:36432838..36434351,2	MCF-7	breast:
6	chr2:36426823..36429485-chr2:36432838..36434351,2	MCF-7	breast:
7	chr2:36375898..36378508-chr2:36382841..36384658,2	K562	blood:
8	chr2:36463029..36465414-chr20:47894852..47896594,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC007401.2.1-5	chr2:36526531-36526973	NONHSAT070076

Variant related genes	Relation type
ENSG00000233752	TF binding region
ENSG00000233752	CpG island
ENSG00000177410	chromatin interactions
ENSG00000124201	chromatin interactions
ENSG00000209042	chromatin interactions

Extended variants
information (count: 6123 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:6123 , 50 per page) page: 1 2 3 4 5 6 7 ... 123

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188540014	chr2:36355635-36355636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs575147862	chr2:36355755-36355756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs371231633	chr2:36355770-36355771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs371153895	chr2:36355788-36355789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs536260013	chr2:36355816-36355817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs554242775	chr2:36355839-36355840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs113042053	chr2:36355868-36355869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs539932971	chr2:36355880-36355881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs565114464	chr2:36355882-36355883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs576958465	chr2:36355934-36355935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs544139778	chr2:36355970-36355971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs562451858	chr2:36356003-36356004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs529891149	chr2:36356007-36356008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs548198944	chr2:36356019-36356020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs560271184	chr2:36356026-36356027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs1397446	chr2:36356031-36356032	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs1881781	chr2:36356038-36356039	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs528822897	chr2:36356085-36356086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs113543341	chr2:36356087-36356088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs192883434	chr2:36356123-36356124	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs17018273	chr2:36356190-36356191	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs544214800	chr2:36356227-36356228	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs74847748	chr2:36356231-36356232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs533931760	chr2:36356251-36356252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs558357630	chr2:36356302-36356303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs576487762	chr2:36356373-36356374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs544004418	chr2:36356376-36356377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs184893152	chr2:36356395-36356396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs188355711	chr2:36356441-36356442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs150001915	chr2:36356468-36356469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs191119329	chr2:36356477-36356478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs183627708	chr2:36356482-36356483	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs36112196	chr2:36356528-36356529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs370982580	chr2:36356532-36356533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs114113908	chr2:36356539-36356540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs375127158	chr2:36356540-36356541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs368032935	chr2:36356543-36356544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs189310006	chr2:36356544-36356545	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs370237784	chr2:36356577-36356578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs373771902	chr2:36356585-36356586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs561088652	chr2:36356587-36356588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs368839923	chr2:36356606-36356607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs551111199	chr2:36356642-36356643	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs34752859	chr2:36356648-36356649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs568652260	chr2:36356659-36356660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs529639656	chr2:36356687-36356688	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs372363076	chr2:36356701-36356702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs547767823	chr2:36356703-36356704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs569246198	chr2:36356721-36356722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs576151586	chr2:36356742-36356743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Breast cancer	21364760	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	18927303	CNVD
Hereditary gingival fibromatosis	19633868	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
Autism	22495309	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:538 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:36354000-36356800	Enhancers	Fetal Brain Male	brain
2	chr2:36354400-36356200	Enhancers	Brain Germinal Matrix	brain
3	chr2:36354800-36356200	Enhancers	Fetal Brain Female	brain
4	chr2:36355200-36357400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr2:36355400-36355800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr2:36355800-36356000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr2:36356000-36357600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr2:36356200-36357200	Weak transcription	Fetal Brain Female	brain
9	chr2:36356200-36357600	Weak transcription	Brain Germinal Matrix	brain
10	chr2:36357400-36357600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr2:36357400-36357600	Enhancers	Fetal Brain Female	brain
12	chr2:36357600-36357800	Enhancers	Brain Germinal Matrix	brain
13	chr2:36357600-36358000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr2:36357600-36360800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr2:36358000-36360200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr2:36360200-36365600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr2:36360800-36365600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr2:36364400-36365200	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr2:36364400-36365200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr2:36364600-36365000	Enhancers	Primary T helper naive cells from peripheral blood	blood
21	chr2:36364600-36365200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
22	chr2:36364600-36365200	Enhancers	Primary T helper cells PMA-I stimulated	--
23	chr2:36364600-36365200	Enhancers	Primary T helper cells fromperipheralblood	blood
24	chr2:36364600-36365200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
25	chr2:36364600-36365400	Enhancers	Primary T cells from cord blood	blood
26	chr2:36364600-36365400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
27	chr2:36364800-36365200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
28	chr2:36364800-36365200	Enhancers	Primary T killer memory cells from peripheral blood	blood
29	chr2:36364800-36365200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr2:36364800-36365200	Enhancers	Thymus	Thymus
31	chr2:36364800-36366000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
32	chr2:36365600-36365800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr2:36365600-36367200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr2:36365800-36366400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr2:36366200-36366800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr2:36366400-36367600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr2:36366600-36367000	Enhancers	Fetal Kidney	kidney
38	chr2:36367000-36367400	Active TSS	Fetal Kidney	kidney
39	chr2:36367200-36367600	Enhancers	Fetal Lung	lung
40	chr2:36367200-36367800	Enhancers	Fetal Stomach	stomach
41	chr2:36373000-36373200	Enhancers	Pancreas	Pancrea
42	chr2:36373000-36374000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
43	chr2:36373200-36375200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
44	chr2:36373800-36374600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
45	chr2:36374000-36374400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
46	chr2:36374200-36374600	Enhancers	GM12878-XiMat	blood
47	chr2:36374600-36375000	Enhancers	Adipose Nuclei	Adipose
48	chr2:36374600-36375000	Flanking Active TSS	GM12878-XiMat	blood
49	chr2:36375000-36375400	Enhancers	GM12878-XiMat	blood
50	chr2:36376400-36376800	Active TSS	Brain Inferior Temporal Lobe	brain

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