Variant report

Variant	nsv876012
Chromosome Location	chr2:233899377-233996429
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3269)
CpG islands
(count:1464)
Chromatin interactive
region (count:39)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:233927900-233928950	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:233931733-233932341	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:233950010-233950414	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:233926792-233926988	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:233956207-233956812	K562	blood:	n/a	n/a
6	ARID3A	chr2:233924409-233924589	HepG2	liver:	n/a	n/a
7	ATF1	chr2:233956160-233956729	K562	blood:	n/a	n/a
8	ATF2	chr2:233945638-233946566	GM12878	blood:	n/a	n/a
9	ATF2	chr2:233943892-233944737	GM12878	blood:	n/a	n/a
10	ATF2	chr2:233925676-233926874	GM12878	blood:	n/a	n/a
11	ATF2	chr2:233945028-233945667	GM12878	blood:	n/a	n/a
12	ATF2	chr2:233924703-233925343	GM12878	blood:	n/a	n/a
13	ATF2	chr2:233918715-233919066	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr2:233946784-233947919	GM12878	blood:	n/a	n/a
15	ATF2	chr2:233949108-233949661	GM12878	blood:	n/a	n/a
16	ATF2	chr2:233964717-233966050	GM12878	blood:	n/a	n/a
17	ATF2	chr2:233949127-233949637	GM12878	blood:	n/a	n/a
18	ATF2	chr2:233916054-233916564	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr2:233945754-233947788	GM12878	blood:	n/a	n/a
20	ATF2	chr2:233935247-233935762	GM12878	blood:	n/a	n/a
21	ATF2	chr2:233951085-233952041	GM12878	blood:	n/a	n/a
22	ATF2	chr2:233989347-233989857	GM12878	blood:	n/a	n/a
23	ATF2	chr2:233951336-233952031	GM12878	blood:	n/a	n/a
24	ATF2	chr2:233964736-233965819	GM12878	blood:	n/a	n/a
25	ATF2	chr2:233944067-233944611	GM12878	blood:	n/a	n/a
26	ATF2	chr2:233932067-233932636	GM12878	blood:	n/a	n/a
27	ATF2	chr2:233927616-233928445	GM12878	blood:	n/a	n/a
28	ATF2	chr2:233926144-233926557	GM12878	blood:	n/a	n/a
29	ATF2	chr2:233940470-233941171	GM12878	blood:	n/a	n/a
30	ATF2	chr2:233935386-233935749	GM12878	blood:	n/a	n/a
31	ATF3	chr2:233956232-233956724	K562	blood:	n/a	n/a
32	BACH1	chr2:233915978-233916530	H1-hESC	embryonic stem cell:	n/a	n/a
33	BATF	chr2:233949182-233949509	GM12878	blood:	n/a	n/a
34	BATF	chr2:233949149-233949577	GM12878	blood:	n/a	n/a
35	BATF	chr2:233944090-233944513	GM12878	blood:	n/a	n/a
36	BATF	chr2:233946817-233947616	GM12878	blood:	n/a	n/a
37	BATF	chr2:233946750-233947688	GM12878	blood:	n/a	n/a
38	BATF	chr2:233965207-233965820	GM12878	blood:	n/a	n/a
39	BATF	chr2:233925703-233926127	GM12878	blood:	n/a	n/a
40	BATF	chr2:233931857-233932228	GM12878	blood:	n/a	n/a
41	BATF	chr2:233945178-233945611	GM12878	blood:	n/a	chr2:233945388-233945399
42	BATF	chr2:233951422-233951982	GM12878	blood:	n/a	n/a
43	BATF	chr2:233973577-233973832	GM12878	blood:	n/a	chr2:233973715-233973726
44	BATF	chr2:233972853-233973092	GM12878	blood:	n/a	n/a
45	BATF	chr2:233945998-233946503	GM12878	blood:	n/a	n/a
46	BATF	chr2:233973514-233973864	GM12878	blood:	n/a	chr2:233973715-233973726
47	BATF	chr2:233926198-233926566	GM12878	blood:	n/a	n/a
48	BATF	chr2:233964802-233965199	GM12878	blood:	n/a	n/a
49	BATF	chr2:233949941-233950275	GM12878	blood:	n/a	n/a
50	BATF	chr2:233945168-233945548	GM12878	blood:	n/a	chr2:233945388-233945399

(count:1464 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:233925165-233925215	CMK	blood:	n/a
2	chr2:233925275-233925325	SAEC	small airway:	n/a
3	chr2:233899331-233899381	HAEpiC	amniotic membrane:	n/a
4	chr2:233924789-233924839	MCF-7	breast:	n/a
5	chr2:233925181-233925231	GM19239	blood:	n/a
6	chr2:233925181-233925231	CMK	blood:	n/a
7	chr2:233924923-233924973	HCM	heart:	n/a
8	chr2:233925165-233925215	ProgFib	skin:	n/a
9	chr2:233925181-233925231	GM12891	blood:	n/a
10	chr2:233924852-233924902	BJ	skin:	n/a
11	chr2:233981999-233982049	SK-N-SH	brain:	n/a
12	chr2:233924852-233924902	CMK	blood:	n/a
13	chr2:233924923-233924973	NT2-D1	testis:	n/a
14	chr2:233924857-233924907	HPAEpiC	pulmonary alveolar:	n/a
15	chr2:233925923-233925973	Jurkat	blood:	n/a
16	chr2:233924801-233924851	SKMC	muscle:	n/a
17	chr2:233924789-233924839	PANC-1	pancreas:	n/a
18	chr2:233927348-233927398	GM12878	blood:	n/a
19	chr2:233981999-233982049	SK-N-MC	brain:	n/a
20	chr2:233899331-233899381	LNCaP	prostate:	n/a
21	chr2:233925275-233925325	HCPEpiC	choroid plexus:	n/a
22	chr2:233927348-233927398	HCPEpiC	choroid plexus:	n/a
23	chr2:233981885-233981935	BE2_C	brain:	n/a
24	chr2:233925165-233925215	SK-N-SH_RA	brain:	n/a
25	chr2:233924857-233924907	HMEC	breast:	n/a
26	chr2:233928423-233928473	HCM	heart:	n/a
27	chr2:233925923-233925973	NH-A	brain:	n/a
28	chr2:233925275-233925325	AoSMC	blood vessel:	n/a
29	chr2:233924713-233924763	AG04449	skin:	fetal
30	chr2:233981788-233981838	NT2-D1	testis:	n/a
31	chr2:233924923-233924973	K562	blood:	n/a
32	chr2:233925923-233925973	IMR90	lung:	fetal
33	chr2:233981788-233981838	GM12892	blood:	n/a
34	chr2:233924801-233924851	SAEC	small airway:	n/a
35	chr2:233981885-233981935	HRPEpiC	eye:	n/a
36	chr2:233925001-233925051	GM12892	blood:	n/a
37	chr2:233925001-233925051	SAEC	small airway:	n/a
38	chr2:233921350-233921400	HEEpiC	esophagus:	n/a
39	chr2:233995465-233995515	HepG2	liver:	n/a
40	chr2:233924852-233924902	K562	blood:	n/a
41	chr2:233916534-233916584	SK-N-SH	brain:	n/a
42	chr2:233995465-233995515	GM12892	blood:	n/a
43	chr2:233925165-233925215	HEEpiC	esophagus:	n/a
44	chr2:233981885-233981935	SK-N-MC	brain:	n/a
45	chr2:233925030-233925080	H1-hESC	embryonic stem cell:	embryo
46	chr2:233924713-233924763	Jurkat	blood:	n/a
47	chr2:233916534-233916584	BJ	skin:	n/a
48	chr2:233899331-233899381	BE2_C	brain:	n/a
49	chr2:233923814-233923864	HUVEC	blood vessel:	n/a
50	chr2:233995465-233995515	A549	lung:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:233932142..233934708-chr2:233937958..233939667,2	K562	blood:
2	chr2:233956193..233959319-chr2:233960178..233964137,4	K562	blood:
3	chr2:233963128..233963777-chr2:234139167..234140126,2	MCF-7	breast:
4	chr2:233912317..233915187-chr2:233920888..233923160,2	K562	blood:
5	chr2:233954509..233957315-chr2:233965664..233967845,2	K562	blood:
6	chr2:233925658..233927822-chr2:233939006..233941097,2	K562	blood:
7	chr2:233970725..233973158-chr2:233974725..233977216,2	MCF-7	breast:
8	chr2:233954328..233956677-chr2:234159445..234161801,2	K562	blood:
9	chr2:233956570..233959566-chr2:233972598..233974662,2	K562	blood:
10	chr2:233955910..233958032-chr2:233958068..233959632,2	K562	blood:
11	chr2:233922323..233923950-chr2:233931960..233934343,2	K562	blood:
12	chr2:233912317..233915187-chr2:233920888..233923160,2	K562	blood:
13	chr2:233923368..233925539-chr2:233928371..233930307,2	K562	blood:
14	chr2:233947227..233949457-chr2:233951983..233954748,2	K562	blood:
15	chr12:77157176..77158389-chr2:233924667..233925187,4	MCF-7	breast:
16	chr2:233914078..233917204-chr2:233917220..233919359,3	MCF-7	breast:
17	chr2:233939365..233942307-chr2:233943913..233949317,5	K562	blood:
18	chr2:233932142..233934708-chr2:233937958..233939667,2	K562	blood:
19	chr2:233914078..233917204-chr2:233917220..233919359,3	MCF-7	breast:
20	chr2:233947227..233949457-chr2:233951983..233954748,2	K562	blood:
21	chr2:233956193..233959319-chr2:233960178..233964137,4	K562	blood:
22	chr2:233994958..233996944-chr2:234001777..234003720,2	K562	blood:
23	chr2:233923263..233925665-chr2:233926706..233928390,2	MCF-7	breast:
24	chr2:233970725..233973158-chr2:233974725..233977216,2	MCF-7	breast:
25	chr2:233963415..233964042-chr2:234159910..234160577,2	MCF-7	breast:
26	chr2:233846888..233847417-chr2:233918381..233919115,2	MCF-7	breast:
27	chr2:233922323..233923950-chr2:233931960..233934343,2	K562	blood:
28	chr2:233982993..233985955-chr2:233987671..233989373,2	K562	blood:
29	chr2:233902627..233904530-chr2:233906961..233909218,2	MCF-7	breast:
30	chr2:233922580..233924412-chr2:233924753..233926303,2	K562	blood:
31	chr2:233938376..233942307-chr2:233943562..233948106,4	K562	blood:
32	chr2:233717958..233718532-chr2:233918679..233919191,2	MCF-7	breast:
33	chr2:233955910..233958032-chr2:233958068..233959632,2	K562	blood:
34	chr2:233902627..233904530-chr2:233906961..233909218,2	MCF-7	breast:
35	chr2:233956570..233959566-chr2:233972598..233974662,2	K562	blood:
36	chr2:233986249..233988176-chr2:233990390..233992004,2	MCF-7	breast:
37	chr16:14580552..14582142-chr2:233993589..233995498,2	MCF-7	breast:
38	chr2:233954509..233957315-chr2:233965664..233967845,2	K562	blood:
39	chr2:233919381..233921351-chr2:233923407..233926039,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NGEF-1	chr2:233980561-233980735	NONHSAT077458
2	lnc-NGEF-1	chr2:233981701-233982377	NONHSAT077458

No data

Variant related genes	Relation type
INPP5D	TF binding region
INPP5D	CpG island
ENSG00000186908	chromatin interactions
ENSG00000085978	chromatin interactions
ENSG00000168918	chromatin interactions

Extended variants
information (count: 4318 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:4318 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2233394	chr2:233899377-233899378	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs538708272	chr2:233899418-233899419	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs2233395	chr2:233899425-233899426	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs145543414	chr2:233899450-233899451	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs373489874	chr2:233899472-233899473	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs147907558	chr2:233899475-233899476	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs201608379	chr2:233899504-233899505	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs376870710	chr2:233899510-233899511	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs568801613	chr2:233899519-233899520	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs147030809	chr2:233899554-233899555	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs376559802	chr2:233899562-233899563	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs370611873	chr2:233899564-233899565	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs200637515	chr2:233899583-233899584	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs184293814	chr2:233899606-233899607	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs188986922	chr2:233899615-233899616	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs201036365	chr2:233899641-233899642	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs192338539	chr2:233899677-233899678	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs201865338	chr2:233899701-233899702	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs368916060	chr2:233899718-233899719	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs553987242	chr2:233899735-233899736	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs576985852	chr2:233899743-233899744	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs373144878	chr2:233899745-233899746	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs546242414	chr2:233899757-233899758	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs111805552	chr2:233899809-233899810	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs562849003	chr2:233899817-233899818	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs140325391	chr2:233899828-233899829	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs541852804	chr2:233899846-233899847	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs561788409	chr2:233899849-233899850	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs527966444	chr2:233899851-233899852	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs547715598	chr2:233899856-233899857	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs570687185	chr2:233899882-233899883	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs2233396	chr2:233899883-233899884	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs533378010	chr2:233899886-233899887	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs552210840	chr2:233899914-233899915	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs568863567	chr2:233899931-233899932	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs73107150	chr2:233899932-233899933	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs547627227	chr2:233899947-233899948	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs568089102	chr2:233900011-233900012	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs534051283	chr2:233900017-233900018	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs145229159	chr2:233900033-233900034	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs554123776	chr2:233900072-233900073	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs11695991	chr2:233900089-233900090	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs545680152	chr2:233900091-233900092	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs556368082	chr2:233900132-233900133	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs149170580	chr2:233900148-233900149	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs111970318	chr2:233900163-233900164	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs561727091	chr2:233900191-233900192	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs572132353	chr2:233900220-233900221	ZNF genes & repeats Genic enhancers Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs541294512	chr2:233900224-233900225	ZNF genes & repeats Genic enhancers Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs564635317	chr2:233900236-233900237	ZNF genes & repeats Genic enhancers Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	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
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cervical cancer	21062161	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chordoma	18071362	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	22429812	CNVD
Bladder cancer	21909424	CNVD
Renal cell carcinoma	21668985	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
prenatal diagnosis	22389664	CNVD
Myelofibrosis	22110671	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Mental retardation	20152051	CNVD
Cancer	21183584	CNVD
Albright''s disease	22277900	CNVD
Brachydactyly-Mental Retardation Syndrome	22470819	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Colorectal cancer	19359472	CNVD
Autism	18414403	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2765 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:233864400-233902800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr2:233888400-233900200	Weak transcription	Esophagus	oesophagus
3	chr2:233891600-233900200	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr2:233897200-233899400	Enhancers	HMEC	breast
5	chr2:233897400-233899400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr2:233897600-233900200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr2:233898200-233899400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr2:233899000-233899400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr2:233899000-233901800	Weak transcription	Osteobl	bone
10	chr2:233899200-233900200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr2:233899400-233900200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr2:233899400-233901800	Weak transcription	HMEC	breast
13	chr2:233900200-233900600	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr2:233900200-233900800	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
15	chr2:233900200-233900800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr2:233900200-233900800	Enhancers	Pancreas	Pancrea
17	chr2:233900200-233901000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr2:233900200-233901000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr2:233900200-233901000	ZNF genes & repeats	Esophagus	oesophagus
20	chr2:233900200-233901000	ZNF genes & repeats	Fetal Kidney	kidney
21	chr2:233900200-233901000	Active TSS	Fetal Lung	lung
22	chr2:233900400-233900600	Enhancers	Spleen	Spleen
23	chr2:233900600-233900800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr2:233900800-233901000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr2:233900800-233909400	Weak transcription	Spleen	Spleen
26	chr2:233901000-233901200	Weak transcription	Esophagus	oesophagus
27	chr2:233901000-233901800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr2:233901000-233901800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr2:233901200-233901400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr2:233901200-233901400	Enhancers	Esophagus	oesophagus
31	chr2:233901800-233902200	Enhancers	HMEC	breast
32	chr2:233902000-233902200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr2:233902000-233902200	Enhancers	Osteobl	bone
34	chr2:233903800-233904800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr2:233904000-233904600	Bivalent Enhancer	HepG2	liver
36	chr2:233905000-233905200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr2:233906600-233907000	Enhancers	Monocytes-CD14+_RO01746	blood
38	chr2:233906800-233907000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
39	chr2:233906800-233907000	Enhancers	Right Atrium	heart
40	chr2:233907000-233907400	Enhancers	Left Ventricle	heart
41	chr2:233907000-233909200	Weak transcription	Right Atrium	heart
42	chr2:233907200-233907400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
43	chr2:233908200-233908800	Enhancers	Liver	Liver
44	chr2:233908200-233908800	Bivalent Enhancer	HepG2	liver
45	chr2:233909200-233909400	Enhancers	Right Atrium	heart
46	chr2:233909400-233915800	Weak transcription	Right Atrium	heart
47	chr2:233912000-233912200	Bivalent Enhancer	Right Ventricle	heart
48	chr2:233912200-233912600	Enhancers	Esophagus	oesophagus
49	chr2:233912400-233915000	Enhancers	Placenta Amnion	Placenta Amnion
50	chr2:233912600-233913600	Weak transcription	Esophagus	oesophagus

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