Variant report

Variant	nsv948636
Chromosome Location	chr3:19335802-19856585
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1491)
CpG islands
(count:916)
Chromatin interactive
region (count:33)
LncRNA
region (count:2)
Mature miRNA
region (count: 1)
miRNA target
sites (count:2)

(count:1491 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:19838885-19838997	K562	blood:	n/a	n/a
2	ARID3A	chr3:19853257-19853541	K562	blood:	n/a	n/a
3	ATF1	chr3:19409997-19410011	K562	blood:	n/a	n/a
4	ATF1	chr3:19785640-19785860	K562	blood:	n/a	n/a
5	ATF2	chr3:19686507-19687102	GM12878	blood:	n/a	n/a
6	ATF2	chr3:19640324-19640769	GM12878	blood:	n/a	n/a
7	ATF2	chr3:19403701-19404244	GM12878	blood:	n/a	n/a
8	ATF2	chr3:19580877-19582458	GM12878	blood:	n/a	n/a
9	ATF2	chr3:19601146-19601590	GM12878	blood:	n/a	n/a
10	ATF2	chr3:19601108-19601992	GM12878	blood:	n/a	n/a
11	ATF2	chr3:19686532-19687019	GM12878	blood:	n/a	n/a
12	ATF2	chr3:19581327-19581963	GM12878	blood:	n/a	n/a
13	ATF2	chr3:19640384-19640732	GM12878	blood:	n/a	n/a
14	ATF2	chr3:19584169-19584688	GM12878	blood:	n/a	n/a
15	ATF2	chr3:19426308-19426774	GM12878	blood:	n/a	n/a
16	BACH1	chr3:19752946-19753205	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr3:19853360-19853374	K562	blood:	n/a	n/a
18	BACH1	chr3:19686696-19686986	H1-hESC	embryonic stem cell:	n/a	chr3:19686699-19686713
19	BATF	chr3:19686580-19687040	GM12878	blood:	n/a	chr3:19686837-19686848
20	BATF	chr3:19811274-19811475	GM12878	blood:	n/a	n/a
21	BATF	chr3:19640369-19640789	GM12878	blood:	n/a	n/a
22	BATF	chr3:19403727-19403944	GM12878	blood:	n/a	n/a
23	BATF	chr3:19754546-19754789	GM12878	blood:	n/a	chr3:19754677-19754688
24	BATF	chr3:19581956-19582329	GM12878	blood:	n/a	chr3:19582154-19582165
25	BATF	chr3:19550247-19550451	GM12878	blood:	n/a	chr3:19550306-19550317
26	BATF	chr3:19403720-19404006	GM12878	blood:	n/a	n/a
27	BATF	chr3:19582043-19582307	GM12878	blood:	n/a	chr3:19582154-19582165
28	BATF	chr3:19640383-19640708	GM12878	blood:	n/a	n/a
29	BATF	chr3:19686760-19686968	GM12878	blood:	n/a	chr3:19686837-19686848
30	BATF	chr3:19811248-19811473	GM12878	blood:	n/a	n/a
31	BCL11A	chr3:19403738-19404052	GM12878	blood:	n/a	n/a
32	BCL11A	chr3:19638004-19638237	GM12878	blood:	n/a	n/a
33	BCL11A	chr3:19686637-19687019	GM12878	blood:	n/a	n/a
34	BCL11A	chr3:19601229-19601543	GM12878	blood:	n/a	chr3:19601271-19601280
35	BCL11A	chr3:19811218-19811466	GM12878	blood:	n/a	n/a
36	BCLAF1	chr3:19601116-19601730	GM12878	blood:	n/a	chr3:19601271-19601280
37	BCLAF1	chr3:19584622-19585088	GM12878	blood:	n/a	n/a
38	BCLAF1	chr3:19581106-19582443	GM12878	blood:	n/a	chr3:19582158-19582167 chr3:19581707-19581716 chr3:19582157-19582166
39	BHLHE40	chr3:19581542-19581870	GM12878	blood:	n/a	n/a
40	BHLHE40	chr3:19403744-19404360	GM12878	blood:	n/a	n/a
41	BHLHE40	chr3:19853210-19853554	K562	blood:	n/a	n/a
42	BRCA1	chr3:19390328-19390581	H1-hESC	embryonic stem cell:	n/a	n/a
43	BRCA1	chr3:19670489-19670609	GM12878	blood:	n/a	n/a
44	CBX3	chr3:19697781-19698060	K562	blood:	n/a	n/a
45	CBX3	chr3:19660443-19660693	K562	blood:	n/a	n/a
46	CBX3	chr3:19697778-19698074	K562	blood:	n/a	n/a
47	CBX3	chr3:19853175-19853607	K562	blood:	n/a	n/a
48	CCNT2	chr3:19853301-19853822	K562	blood:	n/a	n/a
49	CCNT2	chr3:19745165-19745410	K562	blood:	n/a	n/a
50	CCNT2	chr3:19744247-19744413	K562	blood:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:19740602-19740652	HUVEC	blood vessel:	n/a
2	chr3:19740602-19740652	HUVEC	blood vessel:	n/a
3	chr3:19744061-19744111	AG10803	skin:	n/a
4	chr3:19752610-19752660	HPAEpiC	pulmonary alveolar:	n/a
5	chr3:19850542-19850592	U87	brain:	n/a
6	chr3:19440409-19440459	HRPEpiC	eye:	n/a
7	chr3:19850542-19850592	HRCEpiC	kidney:	n/a
8	chr3:19791456-19791506	PANC-1	pancreas:	n/a
9	chr3:19791304-19791354	HCF	heart:	n/a
10	chr3:19744061-19744111	Caco-2	colon:	n/a
11	chr3:19744061-19744111	HEK293	kidney:	embryo
12	chr3:19740602-19740652	BJ	skin:	n/a
13	chr3:19521725-19521775	SKMC	muscle:	n/a
14	chr3:19818187-19818237	K562	blood:	n/a
15	chr3:19740602-19740652	H1-hESC	embryonic stem cell:	embryo
16	chr3:19515924-19515974	SK-N-SH_RA	brain:	n/a
17	chr3:19791456-19791506	GM12891	blood:	n/a
18	chr3:19850542-19850592	LNCaP	prostate:	n/a
19	chr3:19673982-19674032	H1-hESC	embryonic stem cell:	embryo
20	chr3:19576826-19576876	HIPEpiC	eye:	n/a
21	chr3:19576826-19576876	ECC-1	luminal epithelium:	n/a
22	chr3:19521725-19521775	SK-N-SH_RA	brain:	n/a
23	chr3:19791356-19791406	PrEC	prostate:	n/a
24	chr3:19576826-19576876	PrEC	prostate:	n/a
25	chr3:19850542-19850592	NB4	blood:	n/a
26	chr3:19440409-19440459	SKMC	muscle:	n/a
27	chr3:19389409-19389459	GM12891	blood:	n/a
28	chr3:19515924-19515974	HL-60	blood:	n/a
29	chr3:19389409-19389459	NHBE	bronchial:	n/a
30	chr3:19791356-19791406	PANC-1	pancreas:	n/a
31	chr3:19521725-19521775	GM19239	blood:	n/a
32	chr3:19576826-19576876	SK-N-MC	brain:	n/a
33	chr3:19549017-19549067	ProgFib	skin:	n/a
34	chr3:19521725-19521775	HPAEpiC	pulmonary alveolar:	n/a
35	chr3:19818187-19818237	HRE	kidney:	n/a
36	chr3:19791356-19791406	BE2_C	brain:	n/a
37	chr3:19515924-19515974	A549	lung:	n/a
38	chr3:19740602-19740652	SK-N-MC	brain:	n/a
39	chr3:19389409-19389459	NT2-D1	testis:	n/a
40	chr3:19850542-19850592	ECC-1	luminal epithelium:	n/a
41	chr3:19673982-19674032	A549	lung:	n/a
42	chr3:19549017-19549067	PFSK-1	brain:	n/a
43	chr3:19752610-19752660	NH-A	brain:	n/a
44	chr3:19740602-19740652	PANC-1	pancreas:	n/a
45	chr3:19744061-19744111	Hepatocyte	liver:	n/a
46	chr3:19818187-19818237	U87	brain:	n/a
47	chr3:19673982-19674032	HEEpiC	esophagus:	n/a
48	chr3:19740602-19740652	PrEC	prostate:	n/a
49	chr3:19744061-19744111	GM12891	blood:	n/a
50	chr3:19521725-19521775	Hela-S3	cervix:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:19390558..19391094-chr3:19584541..19585367,2	MCF-7	breast:
2	chr3:19106420..19107155-chr3:19584445..19585029,2	MCF-7	breast:
3	chr3:16317176..16319617-chr3:19576040..19578450,2	MCF-7	breast:
4	chr3:19353897..19355847-chr3:19357448..19360229,2	K562	blood:
5	chr3:19801295..19803442-chr3:19807030..19809544,2	K562	blood:
6	chr3:19829915..19832031-chr3:19834488..19836078,2	K562	blood:
7	chr3:19390113..19391205-chr3:19584358..19585952,11	MCF-7	breast:
8	chr3:19389760..19391334-chr3:19907874..19909391,17	MCF-7	breast:
9	chr10:73474420..73475033-chr3:19519900..19520713,2	MCF-7	breast:
10	chr3:19390558..19391094-chr3:19584541..19585367,2	MCF-7	breast:
11	chr3:19747542..19750159-chr3:19752091..19755330,3	MCF-7	breast:
12	chr17:57923494..57925230-chr3:19349261..19351560,2	MCF-7	breast:
13	chr3:19390113..19391205-chr3:19584358..19585952,11	MCF-7	breast:
14	chr3:19443170..19445320-chr3:19453492..19455526,2	K562	blood:
15	chr3:19105973..19107638-chr3:19390145..19391106,4	MCF-7	breast:
16	chr3:19525585..19527422-chr3:19576707..19579689,2	MCF-7	breast:
17	chr3:19801295..19803442-chr3:19807030..19809544,2	K562	blood:
18	chr3:19353897..19355847-chr3:19357448..19360229,2	K562	blood:
19	chr3:19389338..19390161-chr3:19907650..19908872,3	MCF-7	breast:
20	chr3:19747542..19750159-chr3:19752091..19755330,3	MCF-7	breast:
21	chr3:19489514..19491858-chr3:19516874..19519279,2	K562	blood:
22	chr3:19829915..19832031-chr3:19834488..19836078,2	K562	blood:
23	chr3:19679630..19681949-chr3:19683459..19685004,2	K562	blood:
24	chr2:105766716..105768972-chr3:19479211..19481306,2	MCF-7	breast:
25	chr3:19679630..19681949-chr3:19683459..19685004,2	K562	blood:
26	chr3:19106403..19107061-chr3:19390358..19391130,2	MCF-7	breast:
27	chr3:19390433..19391079-chr3:19907967..19908843,4	MCF-7	breast:
28	chr3:19489514..19491858-chr3:19516874..19519279,2	K562	blood:
29	chr3:19443170..19445320-chr3:19453492..19455526,2	K562	blood:
30	chr1:62901559..62902065-chr3:19594424..19594924,2	Hela-S3	cervix:
31	chr3:19525585..19527422-chr3:19576707..19579689,2	MCF-7	breast:
32	chr3:19745768..19748356-chr3:19750935..19754447,3	K562	blood:
33	chr3:19745768..19748356-chr3:19750935..19754447,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EFHB-1	chr3:19729726-19729972	XLOC_003064
2	lnc-EFHB-1	chr3:19717560-19717598	XLOC_003064

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4791	chr3:19356399-19356416	MIMAT0019963

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	KCNH8	hsa-miR-143-3p	chr3:19576050-19576073
2	KCNH8	hsa-miR-143-3p	chr3:19576066-19576072

Variant related genes	Relation type
KCNH8	TF binding region
MIR4791	TF binding region
KCNH8	CpG island
MIR4791	CpG island
ENSG00000201524	chromatin interactions
ENSG00000270739	chromatin interactions
ENSG00000162607	chromatin interactions
ESYT1	miRNA target sites

Extended variants
information (count: 13039 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:13039 , 50 per page) page: 1 2 3 4 5 6 7 ... 261

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7636919	chr3:19335802-19335803	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs537579161	chr3:19335805-19335806	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs566373313	chr3:19335812-19335813	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs557713708	chr3:19335813-19335814	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs533545633	chr3:19335822-19335823	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs59575962	chr3:19335843-19335844	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs567001819	chr3:19335868-19335869	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs183594752	chr3:19335903-19335904	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs555860642	chr3:19335914-19335915	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs577258257	chr3:19335917-19335918	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs372472988	chr3:19335950-19335951	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs117786977	chr3:19335991-19335992	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs188259134	chr3:19336012-19336013	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs533552075	chr3:19336021-19336022	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs560305146	chr3:19336134-19336135	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs553771108	chr3:19336172-19336173	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs191611221	chr3:19336201-19336202	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs542632440	chr3:19336250-19336251	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs79484790	chr3:19336288-19336289	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs576522565	chr3:19336292-19336293	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs377194320	chr3:19336293-19336294	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs553601635	chr3:19336330-19336331	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs369387033	chr3:19336353-19336354	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs12485415	chr3:19336360-19336361	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs542770814	chr3:19336373-19336374	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs371293978	chr3:19336386-19336387	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs115960884	chr3:19336387-19336388	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs562573814	chr3:19336415-19336416	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs563507891	chr3:19336416-19336417	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs576456684	chr3:19336504-19336505	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs545215211	chr3:19336527-19336528	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs530453788	chr3:19336533-19336534	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs548556186	chr3:19336580-19336581	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs76219837	chr3:19336583-19336584	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs531209389	chr3:19336687-19336688	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs549424337	chr3:19336701-19336702	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs571359376	chr3:19336741-19336742	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs199529316	chr3:19336751-19336752	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs184944965	chr3:19336769-19336770	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs139044736	chr3:19336774-19336775	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs564404278	chr3:19336821-19336822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs7639970	chr3:19336826-19336827	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs571059958	chr3:19336876-19336877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs554786703	chr3:19336880-19336881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs577106430	chr3:19336882-19336883	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs554926712	chr3:19336949-19336950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs372497413	chr3:19336961-19336962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs543850903	chr3:19336993-19336994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs149865823	chr3:19336994-19336995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs577315459	chr3:19336997-19336998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Developmental delay	21147756	CNVD
Uveal melanoma	20484589	CNVD
Autism	20531469	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	22495311	CNVD

Chromatin state (count:861 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:19329600-19351400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr3:19333400-19336400	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr3:19333400-19336400	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr3:19333400-19336600	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr3:19334000-19336400	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr3:19334800-19336200	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr3:19334800-19336800	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr3:19335400-19336800	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr3:19335600-19337200	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr3:19336200-19336400	Enhancers	H9 Cell Line	embryonic stem cell
11	chr3:19343000-19343600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr3:19343000-19343800	Enhancers	H9 Cell Line	embryonic stem cell
13	chr3:19343000-19343800	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr3:19343000-19344000	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr3:19343000-19344200	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr3:19343000-19344200	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr3:19343200-19343800	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr3:19343400-19343600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr3:19343400-19344000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
20	chr3:19343400-19344000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr3:19343600-19358200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr3:19344000-19350000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr3:19350000-19350200	Active TSS	Breast Myoepithelial Primary Cells	Breast
24	chr3:19350000-19350400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
25	chr3:19350200-19350400	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
26	chr3:19351400-19352400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr3:19352400-19365000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr3:19358000-19358400	Enhancers	Brain Substantia Nigra	brain
29	chr3:19358200-19358400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr3:19358200-19358600	Enhancers	Brain Angular Gyrus	brain
31	chr3:19358200-19358600	Enhancers	Brain Inferior Temporal Lobe	brain
32	chr3:19358200-19358800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr3:19365000-19367400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr3:19367400-19383600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr3:19370000-19370600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr3:19373800-19374000	Enhancers	Brain Inferior Temporal Lobe	brain
37	chr3:19374000-19378400	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr3:19375400-19375800	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr3:19375400-19375800	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr3:19375400-19375800	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr3:19375400-19375800	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr3:19375400-19375800	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr3:19375400-19376200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr3:19375600-19376000	Enhancers	H1 Cell Line	embryonic stem cell
45	chr3:19375600-19376000	Enhancers	H9 Cell Line	embryonic stem cell
46	chr3:19375600-19376000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr3:19375600-19376000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr3:19378200-19378400	Enhancers	Brain Germinal Matrix	brain
49	chr3:19378400-19378800	Enhancers	Brain Inferior Temporal Lobe	brain
50	chr3:19378400-19379200	Enhancers	Brain Cingulate Gyrus	brain

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