Variant report

Variant	nsv877369
Chromosome Location	chr3:118681771-118824418
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:861)
CpG islands
(count:1100)
Chromatin interactive
region (count:20)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:118753735-118753935	K562	blood:	n/a	n/a
2	ARID3A	chr3:118703634-118704104	K562	blood:	n/a	n/a
3	ARID3A	chr3:118734227-118734231	HepG2	liver:	n/a	n/a
4	ATF1	chr3:118739149-118739350	K562	blood:	n/a	n/a
5	ATF1	chr3:118705608-118705894	K562	blood:	n/a	n/a
6	ATF1	chr3:118703609-118703888	K562	blood:	n/a	n/a
7	ATF1	chr3:118817076-118817276	K562	blood:	n/a	n/a
8	ATF3	chr3:118703574-118703992	K562	blood:	n/a	n/a
9	BACH1	chr3:118684191-118684212	K562	blood:	n/a	n/a
10	BACH1	chr3:118753370-118754199	H1-hESC	embryonic stem cell:	n/a	n/a
11	BHLHE40	chr3:118703611-118703902	K562	blood:	n/a	chr3:118703784-118703805
12	BHLHE40	chr3:118753664-118753967	GM12878	blood:	n/a	chr3:118753861-118753877 chr3:118753762-118753778 chr3:118753864-118753880
13	BHLHE40	chr3:118753613-118754025	K562	blood:	n/a	chr3:118753861-118753877 chr3:118753762-118753778 chr3:118753864-118753880
14	BHLHE40	chr3:118688306-118688376	K562	blood:	n/a	n/a
15	CCNT2	chr3:118753087-118754043	K562	blood:	n/a	n/a
16	CCNT2	chr3:118703639-118703962	K562	blood:	n/a	n/a
17	CEBPB	chr3:118741045-118741288	HepG2	liver:	n/a	chr3:118741136-118741147
18	CEBPB	chr3:118741064-118741238	H1-hESC	embryonic stem cell:	n/a	chr3:118741136-118741147
19	CEBPB	chr3:118778947-118779140	HepG2	liver:	n/a	chr3:118779069-118779080
20	CEBPB	chr3:118708183-118708258	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr3:118737472-118737647	A549	lung:	n/a	n/a
22	CEBPB	chr3:118741075-118741275	A549	lung:	n/a	chr3:118741136-118741147
23	CEBPB	chr3:118745368-118745633	HepG2	liver:	n/a	chr3:118745489-118745500
24	CEBPB	chr3:118740984-118741309	IMR90	lung:	n/a	chr3:118741136-118741147
25	CEBPB	chr3:118741024-118741203	K562	blood:	n/a	chr3:118741136-118741147
26	CEBPB	chr3:118817555-118817690	K562	blood:	n/a	n/a
27	CEBPD	chr3:118703581-118703942	K562	blood:	n/a	n/a
28	CHD1	chr3:118752910-118753656	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD1	chr3:118753827-118753996	GM12878	blood:	n/a	n/a
30	CHD2	chr3:118753658-118753827	HepG2	liver:	n/a	chr3:118753765-118753775
31	CHD2	chr3:118753548-118753681	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr3:118753607-118753878	GM12878	blood:	n/a	chr3:118753765-118753775
33	CREB1	chr3:118753090-118753994	A549	lung:	n/a	n/a
34	CTBP2	chr3:118753482-118754214	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr3:118817536-118817759	Kidney_OC	kidney:	n/a	chr3:118817652-118817670
36	CTCF	chr3:118817560-118817710	Hela-S3	cervix:	n/a	chr3:118817652-118817670
37	CTCF	chr3:118817560-118817710	GM12801	blood:	n/a	chr3:118817652-118817670
38	CTCF	chr3:118803960-118804110	GM12874	blood:	n/a	n/a
39	CTCF	chr3:118817580-118817730	GM12865	blood:	n/a	chr3:118817652-118817670
40	CTCF	chr3:118753474-118754025	A549	lung:	n/a	n/a
41	CTCF	chr3:118753780-118753930	HCT-116	colon:	n/a	n/a
42	CTCF	chr3:118817600-118817750	NB4	blood:	n/a	chr3:118817652-118817670
43	CTCF	chr3:118817620-118817770	HRPEpiC	eye:	n/a	chr3:118817652-118817670
44	CTCF	chr3:118804020-118804170	GM12864	blood:	n/a	n/a
45	CTCF	chr3:118753720-118753870	AG04450	lung:	n/a	n/a
46	CTCF	chr3:118753760-118753910	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr3:118753621-118754064	T-47D	breast:	n/a	n/a
48	CTCF	chr3:118817500-118817650	A549	lung:	n/a	n/a
49	CTCF	chr3:118804092-118804100	GM12878	blood:	n/a	n/a
50	CTCF	chr3:118764029-118764122	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:118753738-118753788	AG10803	skin:	n/a
2	chr3:118705126-118705176	Hela-S3	cervix:	n/a
3	chr3:118753738-118753788	AG10803	skin:	n/a
4	chr3:118705126-118705176	Hela-S3	cervix:	n/a
5	chr3:118706648-118706698	SK-N-SH_RA	brain:	n/a
6	chr3:118753714-118753764	AG10803	skin:	n/a
7	chr3:118792317-118792367	HIPEpiC	eye:	n/a
8	chr3:118734756-118734806	LNCaP	prostate:	n/a
9	chr3:118792317-118792367	HCPEpiC	choroid plexus:	n/a
10	chr3:118686312-118686362	HRCEpiC	kidney:	n/a
11	chr3:118734756-118734806	AG10803	skin:	n/a
12	chr3:118753738-118753788	HCF	heart:	n/a
13	chr3:118754097-118754147	RPTEC	kidney:	n/a
14	chr3:118753714-118753764	GM12891	blood:	n/a
15	chr3:118753005-118753055	AG09309	skin:	n/a
16	chr3:118753005-118753055	NT2-D1	testis:	n/a
17	chr3:118753871-118753921	CMK	blood:	n/a
18	chr3:118753871-118753921	ovcar-3	ovarian:	n/a
19	chr3:118753871-118753921	HMEC	breast:	n/a
20	chr3:118753005-118753055	HCPEpiC	choroid plexus:	n/a
21	chr3:118750463-118750513	IMR90	lung:	fetal
22	chr3:118753714-118753764	BE2_C	brain:	n/a
23	chr3:118753005-118753055	H1-hESC	embryonic stem cell:	embryo
24	chr3:118757898-118757948	CMK	blood:	n/a
25	chr3:118753705-118753755	HAEpiC	amniotic membrane:	n/a
26	chr3:118753705-118753755	NH-A	brain:	n/a
27	chr3:118753660-118753710	MCF-7	breast:	n/a
28	chr3:118734756-118734806	NB4	blood:	n/a
29	chr3:118753705-118753755	AG09309	skin:	n/a
30	chr3:118686312-118686362	SK-N-MC	brain:	n/a
31	chr3:118792317-118792367	HPAEpiC	pulmonary alveolar:	n/a
32	chr3:118753707-118753757	AoSMC	blood vessel:	n/a
33	chr3:118706648-118706698	GM12891	blood:	n/a
34	chr3:118706648-118706698	CMK	blood:	n/a
35	chr3:118753705-118753755	HIPEpiC	eye:	n/a
36	chr3:118753707-118753757	AG04449	skin:	fetal
37	chr3:118686312-118686362	LNCaP	prostate:	n/a
38	chr3:118706648-118706698	AG04449	skin:	fetal
39	chr3:118754376-118754426	HEEpiC	esophagus:	n/a
40	chr3:118754097-118754147	IMR90	lung:	fetal
41	chr3:118753705-118753755	SK-N-MC	brain:	n/a
42	chr3:118750463-118750513	PFSK-1	brain:	n/a
43	chr3:118792317-118792367	HRCEpiC	kidney:	n/a
44	chr3:118734756-118734806	HIPEpiC	eye:	n/a
45	chr3:118753660-118753710	GM12892	blood:	n/a
46	chr3:118706648-118706698	HCM	heart:	n/a
47	chr3:118753705-118753755	CMK	blood:	n/a
48	chr3:118705126-118705176	PFSK-1	brain:	n/a
49	chr3:118753738-118753788	HCT-116	colon:	n/a
50	chr3:118753705-118753755	HNPCEpiC	eye:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:118600900..118602263-chr3:118817111..118818102,7	MCF-7	breast:
2	chr3:118780729..118783547-chr3:118785374..118787661,2	K562	blood:
3	chr19:34079834..34082285-chr3:118740671..118743263,2	MCF-7	breast:
4	chr3:118601857..118602685-chr3:118817256..118818095,2	MCF-7	breast:
5	chr3:118781130..118783547-chr3:118786161..118788492,2	K562	blood:
6	chr3:118600892..118601643-chr3:118803705..118804296,2	K562	blood:
7	chr3:118683148..118684956-chr3:118685063..118686921,2	K562	blood:
8	chr3:118753444..118753993-chr3:118815481..118816221,2	MCF-7	breast:
9	chr20:55795723..55796346-chr3:118817504..118818179,2	MCF-7	breast:
10	chr3:118683148..118684956-chr3:118685063..118686921,2	K562	blood:
11	chr3:118604102..118604821-chr3:118803607..118804317,2	MCF-7	breast:
12	chr3:118781130..118783547-chr3:118786161..118788492,2	K562	blood:
13	chr3:118603251..118604473-chr3:118817204..118818111,6	K562	blood:
14	chr3:118603511..118604421-chr3:118817152..118818248,5	MCF-7	breast:
15	chr3:116489803..116490556-chr3:118816385..118817077,2	K562	blood:
16	chr3:118601491..118603517-chr3:118818904..118820959,2	MCF-7	breast:
17	chr3:118603583..118604395-chr3:118755020..118755749,3	MCF-7	breast:
18	chr3:118600918..118601876-chr3:118816856..118817797,3	K562	blood:
19	chr3:118780729..118783547-chr3:118785374..118787661,2	K562	blood:
20	chr3:118603151..118604416-chr3:118816830..118818388,23	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-B4GALT4-2	chr3:118823991-118824052	NONHSAT091373

No data

Variant related genes	Relation type
IGSF11	TF binding region
IGSF11	CpG island
ENSG00000144847	chromatin interactions
ENSG00000232429	chromatin interactions

Extended variants
information (count: 3533 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:3533 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6795936	chr3:118681771-118681772	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs141769938	chr3:118681778-118681779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs574892604	chr3:118681837-118681838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs6786886	chr3:118681862-118681863	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs554656918	chr3:118681896-118681897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs528141043	chr3:118681902-118681903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs572804735	chr3:118681939-118681940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs181528365	chr3:118681964-118681965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs559950511	chr3:118681988-118681989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs533700541	chr3:118681996-118681997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs150595337	chr3:118681997-118681998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs138578264	chr3:118682051-118682052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs368957001	chr3:118682054-118682055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs72968624	chr3:118682061-118682062	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs547886176	chr3:118682238-118682239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs186539728	chr3:118682270-118682271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs540953247	chr3:118682271-118682272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs528544094	chr3:118682312-118682313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs201389480	chr3:118682316-118682317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs546424779	chr3:118682344-118682345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs571088563	chr3:118682365-118682366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs142829185	chr3:118682380-118682381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs118141071	chr3:118682412-118682413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs569015787	chr3:118682440-118682441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs9849182	chr3:118682478-118682479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs568005364	chr3:118682509-118682510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs191839559	chr3:118682518-118682519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs376630910	chr3:118682525-118682526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs376681765	chr3:118682553-118682554	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs572907218	chr3:118682577-118682578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs533853988	chr3:118682583-118682584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs553629549	chr3:118682585-118682586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs578214439	chr3:118682594-118682595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs116184117	chr3:118682626-118682627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs563976446	chr3:118682634-118682635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs556448058	chr3:118682635-118682636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs370006346	chr3:118682711-118682712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs374127443	chr3:118682731-118682732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs575822465	chr3:118682768-118682769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs182932634	chr3:118682816-118682817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs561110277	chr3:118682867-118682868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs185757813	chr3:118682893-118682894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs539369918	chr3:118682909-118682910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs367725317	chr3:118682929-118682930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs191450775	chr3:118682969-118682970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs532183000	chr3:118682978-118682979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs550313191	chr3:118683002-118683003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs112114703	chr3:118683013-118683014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs569154263	chr3:118683128-118683129	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs536122661	chr3:118683202-118683203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Developmental delay	22180640	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Myelofibrosis	22110671	CNVD
Characteristic facial feature	22180640	CNVD
hypoplastic male genitals	22180640	CNVD
postnatal overgrowth	22180640	CNVD
lymphocytic leukemia	21291569	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Glioblastoma multiforme	22286061	CNVD

Chromatin state (count:1040 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:118675600-118684800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr3:118676800-118684000	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr3:118679000-118688200	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr3:118680000-118683800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr3:118680200-118681800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr3:118680200-118684600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr3:118680200-118684600	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr3:118680200-118684800	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr3:118680200-118686600	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr3:118680200-118686600	Weak transcription	Skeletal Muscle Female	skeletal muscle
11	chr3:118680200-118688200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr3:118680200-118688200	Weak transcription	Ovary	ovary
13	chr3:118680800-118681800	Weak transcription	Brain Anterior Caudate	brain
14	chr3:118681200-118694000	Enhancers	Brain Substantia Nigra	brain
15	chr3:118681400-118683400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr3:118681400-118683400	Enhancers	Brain Cingulate Gyrus	brain
17	chr3:118681400-118684000	Enhancers	Brain Inferior Temporal Lobe	brain
18	chr3:118681400-118690000	Enhancers	Brain Hippocampus Middle	brain
19	chr3:118681600-118682200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
20	chr3:118681600-118683400	Enhancers	Brain Angular Gyrus	brain
21	chr3:118681800-118683400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr3:118681800-118692800	Enhancers	Brain Anterior Caudate	brain
23	chr3:118682200-118685400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr3:118683400-118684400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr3:118683400-118684600	Weak transcription	Brain Cingulate Gyrus	brain
26	chr3:118683400-118685000	Weak transcription	Brain Angular Gyrus	brain
27	chr3:118683400-118696200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr3:118683800-118689000	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr3:118684000-118684200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr3:118684000-118684400	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr3:118684000-118687400	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr3:118684200-118685000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr3:118684400-118685800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr3:118684400-118690000	Enhancers	Brain Inferior Temporal Lobe	brain
35	chr3:118684600-118685400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr3:118684600-118687600	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr3:118684600-118690200	Enhancers	Brain Cingulate Gyrus	brain
38	chr3:118684800-118687600	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr3:118684800-118690200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr3:118684800-118694000	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr3:118685000-118685800	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr3:118685000-118688800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr3:118685000-118690000	Enhancers	Brain Angular Gyrus	brain
44	chr3:118685400-118686400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr3:118685400-118689400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
46	chr3:118685600-118685800	Enhancers	H1 Cell Line	embryonic stem cell
47	chr3:118685600-118685800	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr3:118685600-118685800	Enhancers	Psoas Muscle	Psoas
49	chr3:118685600-118685800	Enhancers	Right Atrium	heart
50	chr3:118685600-118685800	Enhancers	HSMMtube	muscle

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