Variant report

Variant	esv2752813
Chromosome Location	chr15:58461006-58507064
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1051)
CpG islands
(count:184)
Chromatin interactive
region (count:58)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1051 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:58474774-58475043	K562	blood:	n/a	n/a
2	ARID3A	chr15:58505087-58505435	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:58469488-58469705	K562	blood:	n/a	n/a
4	ARID3A	chr15:58481416-58481549	K562	blood:	n/a	n/a
5	ARID3A	chr15:58474813-58474931	HepG2	liver:	n/a	n/a
6	ARID3A	chr15:58495768-58496124	K562	blood:	n/a	n/a
7	ARID3A	chr15:58505066-58505527	K562	blood:	n/a	n/a
8	ARID3A	chr15:58468984-58469215	K562	blood:	n/a	n/a
9	ARID3A	chr15:58471639-58472310	K562	blood:	n/a	n/a
10	ATF1	chr15:58471551-58472328	K562	blood:	n/a	n/a
11	ATF1	chr15:58495748-58496112	K562	blood:	n/a	n/a
12	ATF3	chr15:58495720-58496028	K562	blood:	n/a	n/a
13	BACH1	chr15:58495705-58496032	K562	blood:	n/a	n/a
14	BHLHE40	chr15:58495748-58496097	K562	blood:	n/a	n/a
15	BHLHE40	chr15:58505116-58505389	K562	blood:	n/a	n/a
16	BHLHE40	chr15:58481398-58481609	K562	blood:	n/a	n/a
17	BHLHE40	chr15:58492948-58493214	K562	blood:	n/a	n/a
18	BHLHE40	chr15:58474715-58475024	K562	blood:	n/a	n/a
19	BHLHE40	chr15:58471584-58472313	K562	blood:	n/a	n/a
20	BRCA1	chr15:58474911-58475014	HepG2	liver:	n/a	n/a
21	CBX3	chr15:58474577-58475057	K562	blood:	n/a	n/a
22	CBX3	chr15:58471557-58472681	K562	blood:	n/a	n/a
23	CBX3	chr15:58481267-58481692	K562	blood:	n/a	n/a
24	CBX3	chr15:58468921-58469277	K562	blood:	n/a	n/a
25	CCNT2	chr15:58471636-58472335	K562	blood:	n/a	n/a
26	CCNT2	chr15:58469002-58469202	K562	blood:	n/a	n/a
27	CCNT2	chr15:58481241-58481441	K562	blood:	n/a	n/a
28	CCNT2	chr15:58495434-58496123	K562	blood:	n/a	n/a
29	CEBPB	chr15:58505321-58505560	HepG2	liver:	n/a	n/a
30	CEBPB	chr15:58495702-58496003	K562	blood:	n/a	n/a
31	CEBPB	chr15:58474855-58475071	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr15:58495554-58496176	IMR90	lung:	n/a	n/a
33	CEBPB	chr15:58495707-58496018	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr15:58495614-58496078	K562	blood:	n/a	n/a
35	CEBPB	chr15:58505132-58505565	A549	lung:	n/a	n/a
36	CEBPB	chr15:58471763-58472379	K562	blood:	n/a	n/a
37	CEBPB	chr15:58506232-58506470	Hela-S3	cervix:	n/a	chr15:58506368-58506379
38	CEBPB	chr15:58506199-58506499	A549	lung:	n/a	chr15:58506368-58506379
39	CEBPB	chr15:58506198-58506480	HepG2	liver:	n/a	chr15:58506368-58506379
40	CEBPB	chr15:58482858-58482945	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr15:58506207-58506542	IMR90	lung:	n/a	chr15:58506368-58506379
42	CEBPB	chr15:58495513-58496192	K562	blood:	n/a	n/a
43	CEBPB	chr15:58471862-58472269	K562	blood:	n/a	n/a
44	CEBPB	chr15:58471903-58472210	K562	blood:	n/a	n/a
45	CEBPB	chr15:58506192-58506548	K562	blood:	n/a	chr15:58506368-58506379
46	CEBPB	chr15:58506161-58506534	K562	blood:	n/a	chr15:58506368-58506379
47	CEBPD	chr15:58471765-58472434	K562	blood:	n/a	n/a
48	CEBPD	chr15:58495626-58496185	K562	blood:	n/a	n/a
49	CEBPD	chr15:58495615-58496179	K562	blood:	n/a	n/a
50	CEBPD	chr15:58471712-58472421	K562	blood:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:58474918-58474968	AG09319	gingival:	n/a
2	chr15:58474918-58474968	AG09319	gingival:	n/a
3	chr15:58496278-58496328	U87	brain:	n/a
4	chr15:58474918-58474968	NHDF-neo	bronchial:	n/a
5	chr15:58474918-58474968	IMR90	lung:	fetal
6	chr15:58474918-58474968	Caco-2	colon:	n/a
7	chr15:58474918-58474968	AG04450	lung:	fetal
8	chr15:58496278-58496328	NHDF-neo	bronchial:	n/a
9	chr15:58474918-58474968	HCT-116	colon:	n/a
10	chr15:58476720-58476770	HRCEpiC	kidney:	n/a
11	chr15:58496278-58496328	ProgFib	skin:	n/a
12	chr15:58474918-58474968	U87	brain:	n/a
13	chr15:58474918-58474968	AG10803	skin:	n/a
14	chr15:58496278-58496328	ECC-1	luminal epithelium:	n/a
15	chr15:58476720-58476770	HCM	heart:	n/a
16	chr15:58474918-58474968	HAEpiC	amniotic membrane:	n/a
17	chr15:58496278-58496328	ovcar-3	ovarian:	n/a
18	chr15:58476720-58476770	SKMC	muscle:	n/a
19	chr15:58474918-58474968	HEEpiC	esophagus:	n/a
20	chr15:58496278-58496328	HAEpiC	amniotic membrane:	n/a
21	chr15:58474918-58474968	AoSMC	blood vessel:	n/a
22	chr15:58474918-58474968	HEK293	kidney:	embryo
23	chr15:58496278-58496328	PFSK-1	brain:	n/a
24	chr15:58496278-58496328	HepG2	liver:	n/a
25	chr15:58476720-58476770	SAEC	small airway:	n/a
26	chr15:58476720-58476770	T-47D	breast:	n/a
27	chr15:58496278-58496328	SKMC	muscle:	n/a
28	chr15:58496278-58496328	AG10803	skin:	n/a
29	chr15:58496278-58496328	H1-hESC	embryonic stem cell:	embryo
30	chr15:58476720-58476770	IMR90	lung:	fetal
31	chr15:58476720-58476770	AG09309	skin:	n/a
32	chr15:58496278-58496328	RPTEC	kidney:	n/a
33	chr15:58476720-58476770	HUVEC	blood vessel:	n/a
34	chr15:58476720-58476770	U87	brain:	n/a
35	chr15:58496278-58496328	HRPEpiC	eye:	n/a
36	chr15:58476720-58476770	SK-N-MC	brain:	n/a
37	chr15:58496278-58496328	GM12891	blood:	n/a
38	chr15:58476720-58476770	K562	blood:	n/a
39	chr15:58496278-58496328	LNCaP	prostate:	n/a
40	chr15:58474918-58474968	HepG2	liver:	n/a
41	chr15:58496278-58496328	GM19239	blood:	n/a
42	chr15:58496278-58496328	HL-60	blood:	n/a
43	chr15:58476720-58476770	Caco-2	colon:	n/a
44	chr15:58476720-58476770	HPAEpiC	pulmonary alveolar:	n/a
45	chr15:58476720-58476770	NT2-D1	testis:	n/a
46	chr15:58496278-58496328	HIPEpiC	eye:	n/a
47	chr15:58474918-58474968	Hela-S3	cervix:	n/a
48	chr15:58476720-58476770	SK-N-SH	brain:	n/a
49	chr15:58474918-58474968	HRE	kidney:	n/a
50	chr15:58476720-58476770	GM12878	blood:	n/a

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:58356201..58358538-chr15:58469656..58471304,3	K562	blood:
2	chr15:58473604..58477327-chr15:58478403..58482264,4	K562	blood:
3	chr15:58346910..58349954-chr15:58473390..58475572,3	K562	blood:
4	chr15:58355281..58357769-chr15:58504795..58507676,2	K562	blood:
5	chr15:58335119..58336017-chr15:58474443..58475104,3	K562	blood:
6	chr15:58402733..58404852-chr15:58471216..58473457,2	K562	blood:
7	chr15:58481646..58483822-chr15:58485314..58486838,2	K562	blood:
8	chr15:58480797..58483752-chr15:58496881..58499713,2	K562	blood:
9	chr15:58348390..58350453-chr15:58469668..58473033,3	K562	blood:
10	chr15:58467290..58469519-chr15:58470114..58472151,2	K562	blood:
11	chr15:58362749..58363649-chr15:58474448..58475386,2	MCF-7	breast:
12	chr15:58157203..58158392-chr15:58474458..58475600,4	K562	blood:
13	chr15:58479445..58483146-chr15:58484303..58486814,3	K562	blood:
14	chr15:58355374..58360159-chr15:58469656..58474821,10	K562	blood:
15	chr15:58504905..58505726-chr15:58513648..58514433,4	MCF-7	breast:
16	chr15:58355812..58358960-chr15:58474345..58476655,3	K562	blood:
17	chr15:57615195..57617935-chr15:58470715..58472691,2	K562	blood:
18	chr15:58304704..58306626-chr15:58479372..58481388,2	K562	blood:
19	chr15:58461476..58463805-chr15:58468406..58470594,2	K562	blood:
20	chr15:58261336..58261843-chr15:58474684..58475338,2	K562	blood:
21	chr15:58471240..58473438-chr15:58477636..58480344,3	K562	blood:
22	chr15:58471240..58473438-chr15:58477636..58480344,3	K562	blood:
23	chr15:58504304..58505276-chr15:58513365..58514203,2	MCF-7	breast:
24	chr15:58505038..58505764-chr15:58519727..58520416,2	K562	blood:
25	chr15:58358218..58360333-chr15:58503772..58505301,2	K562	blood:
26	chr15:58464019..58467002-chr15:58469139..58471766,2	K562	blood:
27	chr15:58473604..58477327-chr15:58478403..58482264,4	K562	blood:
28	chr15:58158497..58159034-chr15:58474354..58475384,5	K562	blood:
29	chr15:58481646..58483822-chr15:58485314..58486838,2	K562	blood:
30	chr15:58402611..58405043-chr15:58470858..58473947,6	K562	blood:
31	chr15:58351815..58354737-chr15:58471635..58473722,2	K562	blood:
32	chr15:58461476..58463805-chr15:58468406..58470594,2	K562	blood:
33	chr15:58504810..58506580-chr15:59063444..59065345,2	K562	blood:
34	chr15:58357891..58359438-chr15:58472040..58474071,2	K562	blood:
35	chr15:58369765..58370364-chr15:58474440..58475412,7	K562	blood:
36	chr15:58480377..58482794-chr15:58490469..58493336,2	K562	blood:
37	chr15:58356916..58358526-chr15:58478594..58480634,2	K562	blood:
38	chr15:58464019..58467002-chr15:58469139..58471766,2	K562	blood:
39	chr15:58474504..58475220-chr15:58513550..58514293,3	K562	blood:
40	chr15:58505175..58505781-chr15:59784803..59785341,3	K562	blood:
41	chr15:58505288..58505802-chr15:59820824..59821742,2	K562	blood:
42	chr15:58407522..58408442-chr15:58474456..58475377,4	K562	blood:
43	chr15:58467290..58469519-chr15:58470114..58472151,2	K562	blood:
44	chr15:58358505..58359071-chr15:58474691..58475417,2	K562	blood:
45	chr15:58369556..58370249-chr15:58474458..58475050,3	MCF-7	breast:
46	chr15:58305878..58307859-chr15:58469628..58472033,2	K562	blood:
47	chr15:58369515..58370275-chr15:58474521..58475420,3	MCF-7	breast:
48	chr15:58505987..58508184-chr15:59784928..59787328,2	K562	blood:
49	chr15:58260270..58262441-chr15:58476385..58479078,2	K562	blood:
50	chr15:58011774..58013283-chr15:58488881..58491774,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AQP9-2	chr15:58492805-58493217	NONHSAT044101

No data

Variant related genes	Relation type
ENSG00000240934	TF binding region
ENSG00000240934	CpG island
ENSG00000128923	chromatin interactions
ENSG00000128918	chromatin interactions
ENSG00000259285	chromatin interactions
ENSG00000261219	chromatin interactions
ENSG00000240934	chromatin interactions

Extended variants
information (count: 2069 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:2069 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2414544	chr15:58461006-58461007	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs143046203	chr15:58461012-58461013	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs528305816	chr15:58461022-58461023	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs148191326	chr15:58461025-58461026	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs117874817	chr15:58461037-58461038	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs114068398	chr15:58461042-58461043	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs550318200	chr15:58461061-58461062	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs141691093	chr15:58461066-58461067	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs192968303	chr15:58461074-58461075	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs185049447	chr15:58461176-58461177	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs566252535	chr15:58461190-58461191	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs536005341	chr15:58461192-58461193	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs2899617	chr15:58461222-58461223	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs568471435	chr15:58461254-58461255	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs2414545	chr15:58461270-58461271	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs557075703	chr15:58461326-58461327	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs190291055	chr15:58461346-58461347	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs73426179	chr15:58461431-58461432	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs552878049	chr15:58461526-58461527	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs376671235	chr15:58461542-58461543	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs537128013	chr15:58461554-58461555	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs181742994	chr15:58461644-58461645	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs186262663	chr15:58461666-58461667	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs561785512	chr15:58461694-58461695	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs189490395	chr15:58461712-58461713	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs17821086	chr15:58461738-58461739	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs145301497	chr15:58461742-58461743	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs532982849	chr15:58461786-58461787	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs138036245	chr15:58461805-58461806	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs12905045	chr15:58461814-58461815	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs116985409	chr15:58461866-58461867	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs73426180	chr15:58461878-58461879	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs548803201	chr15:58461881-58461882	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs142528016	chr15:58461916-58461917	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs559174798	chr15:58461928-58461929	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs537139824	chr15:58461933-58461934	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs528380496	chr15:58461947-58461948	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs180789116	chr15:58461952-58461953	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs77293623	chr15:58461995-58461996	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs73426183	chr15:58462023-58462024	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs111455733	chr15:58462025-58462026	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs571465117	chr15:58462029-58462030	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs138665893	chr15:58462038-58462039	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs149320873	chr15:58462064-58462065	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs3784248	chr15:58462074-58462075	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs147736449	chr15:58462093-58462094	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs377219758	chr15:58462103-58462104	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs186207581	chr15:58462118-58462119	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs144703149	chr15:58462138-58462139	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs139820747	chr15:58462231-58462232	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:272 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:58441000-58463800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr15:58451200-58481000	Strong transcription	Primary neutrophils fromperipheralblood	blood
3	chr15:58454800-58471400	Weak transcription	Spleen	Spleen
4	chr15:58457800-58461200	Enhancers	HepG2	liver
5	chr15:58458400-58463400	Weak transcription	Fetal Muscle Leg	muscle
6	chr15:58458400-58477800	Strong transcription	Liver	Liver
7	chr15:58459800-58461800	Strong transcription	Monocytes-CD14+_RO01746	blood
8	chr15:58460000-58461400	Weak transcription	K562	blood
9	chr15:58461400-58462400	Enhancers	K562	blood
10	chr15:58461600-58461800	Enhancers	Pancreas	Pancrea
11	chr15:58461800-58464000	Weak transcription	Monocytes-CD14+_RO01746	blood
12	chr15:58461800-58473000	Weak transcription	Pancreas	Pancrea
13	chr15:58462400-58467600	Weak transcription	K562	blood
14	chr15:58463400-58464000	Enhancers	Fetal Muscle Leg	muscle
15	chr15:58463600-58464200	Enhancers	HSMM	muscle
16	chr15:58463800-58464000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr15:58464000-58464600	Enhancers	HSMMtube	muscle
18	chr15:58464000-58468400	Strong transcription	Monocytes-CD14+_RO01746	blood
19	chr15:58464400-58464800	Enhancers	Fetal Lung	lung
20	chr15:58465400-58465600	Weak transcription	Primary monocytes fromperipheralblood	blood
21	chr15:58465600-58467400	Strong transcription	Primary monocytes fromperipheralblood	blood
22	chr15:58467400-58474600	Weak transcription	Primary monocytes fromperipheralblood	blood
23	chr15:58467600-58469800	Enhancers	K562	blood
24	chr15:58468400-58470800	Weak transcription	Monocytes-CD14+_RO01746	blood
25	chr15:58469800-58470800	Weak transcription	K562	blood
26	chr15:58470600-58471800	Enhancers	HUVEC	blood vessel
27	chr15:58470800-58471200	Enhancers	K562	blood
28	chr15:58470800-58473200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr15:58470800-58473800	Strong transcription	Monocytes-CD14+_RO01746	blood
30	chr15:58471000-58471800	Enhancers	NHEK	skin
31	chr15:58471000-58473200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr15:58471000-58473200	Enhancers	HMEC	breast
33	chr15:58471200-58472600	Flanking Active TSS	K562	blood
34	chr15:58471200-58473000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr15:58471400-58471600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr15:58471400-58471600	Enhancers	Right Atrium	heart
37	chr15:58471400-58472400	Enhancers	Left Ventricle	heart
38	chr15:58471400-58472400	Genic enhancers	Spleen	Spleen
39	chr15:58471400-58472600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr15:58471600-58472600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr15:58471600-58481200	Weak transcription	Right Atrium	heart
42	chr15:58471800-58472000	Flanking Active TSS	NHEK	skin
43	chr15:58471800-58472200	Enhancers	Fetal Heart	heart
44	chr15:58471800-58472200	Enhancers	HSMM	muscle
45	chr15:58471800-58472200	Enhancers	NH-A	brain
46	chr15:58471800-58472400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr15:58471800-58472600	Flanking Active TSS	HUVEC	blood vessel
48	chr15:58471800-58472600	Enhancers	NHDF-Ad	bronchial
49	chr15:58471800-58472800	Enhancers	Muscle Satellite Cultured Cells	--
50	chr15:58471800-58473000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links