Variant report

Variant	nsv428603
Chromosome Location	chr13:66517170-66677184
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:608)
CpG islands
(count:183)
Chromatin interactive
region (count:10)
LncRNA
region (count:4)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:608 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:66648258-66648447	K562	blood:	n/a	n/a
2	ARID3A	chr13:66650602-66650906	K562	blood:	n/a	n/a
3	ARID3A	chr13:66651230-66651680	K562	blood:	n/a	n/a
4	ARID3A	chr13:66643768-66644097	K562	blood:	n/a	n/a
5	ATF1	chr13:66648256-66648525	K562	blood:	n/a	n/a
6	ATF1	chr13:66643737-66644023	K562	blood:	n/a	n/a
7	ATF1	chr13:66650593-66650896	K562	blood:	n/a	n/a
8	BHLHE40	chr13:66648396-66648557	K562	blood:	n/a	n/a
9	CBX3	chr13:66643667-66644035	K562	blood:	n/a	n/a
10	CCNT2	chr13:66617039-66617239	K562	blood:	n/a	n/a
11	CCNT2	chr13:66589547-66589747	K562	blood:	n/a	n/a
12	CEBPB	chr13:66559601-66560095	MCF-7	breast:	n/a	n/a
13	CEBPB	chr13:66605714-66605963	A549	lung:	n/a	chr13:66605818-66605829
14	CEBPB	chr13:66605650-66606010	IMR90	lung:	n/a	chr13:66605818-66605829
15	CEBPB	chr13:66650603-66650906	K562	blood:	n/a	n/a
16	CEBPB	chr13:66569441-66569593	IMR90	lung:	n/a	n/a
17	CEBPB	chr13:66650577-66650900	K562	blood:	n/a	n/a
18	CEBPB	chr13:66650566-66650902	IMR90	lung:	n/a	n/a
19	CEBPB	chr13:66612357-66612666	MCF-7	breast:	n/a	n/a
20	CEBPB	chr13:66574571-66574786	HepG2	liver:	n/a	chr13:66574676-66574685 chr13:66574675-66574686 chr13:66574674-66574685
21	CEBPB	chr13:66605687-66605966	K562	blood:	n/a	chr13:66605818-66605829
22	CEBPB	chr13:66651488-66651782	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr13:66605742-66605955	H1-hESC	embryonic stem cell:	n/a	chr13:66605818-66605829
24	CEBPB	chr13:66539663-66539995	IMR90	lung:	n/a	n/a
25	CEBPB	chr13:66651507-66651735	K562	blood:	n/a	n/a
26	CEBPB	chr13:66571439-66571773	IMR90	lung:	n/a	n/a
27	CEBPB	chr13:66585133-66585269	A549	lung:	n/a	n/a
28	CEBPB	chr13:66559705-66560073	MCF-7	breast:	n/a	n/a
29	CEBPB	chr13:66605646-66606003	HepG2	liver:	n/a	chr13:66605818-66605829
30	CTCF	chr13:66635930-66635964	K562	blood:	n/a	n/a
31	CTCF	chr13:66541220-66541370	HFF-Myc	foreskin:	n/a	n/a
32	CTCF	chr13:66560000-66560150	HCT-116	colon:	n/a	n/a
33	CTCF	chr13:66541220-66541370	NHEK	skin:	n/a	n/a
34	CTCF	chr13:66541200-66541350	MCF-7	breast:	n/a	n/a
35	CTCF	chr13:66541180-66541330	HUVEC	blood vessel:	n/a	n/a
36	CTCF	chr13:66541220-66541370	BE2_C	brain:	n/a	n/a
37	CTCF	chr13:66541140-66541290	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr13:66541160-66541310	HRPEpiC	eye:	n/a	n/a
39	CTCF	chr13:66541180-66541330	AG09319	gingival:	n/a	n/a
40	CTCF	chr13:66541107-66541419	HUVEC	blood vessel:	n/a	n/a
41	CTCF	chr13:66540851-66541569	A549	lung:	n/a	n/a
42	CTCF	chr13:66559940-66560090	A549	lung:	n/a	n/a
43	CTCF	chr13:66541120-66541270	GM12873	blood:	n/a	n/a
44	CTCF	chr13:66541140-66541290	MCF-7	breast:	n/a	n/a
45	CTCF	chr13:66540964-66541442	A549	lung:	n/a	n/a
46	CTCF	chr13:66541240-66541390	WI-38	lung:	n/a	n/a
47	CTCF	chr13:66540981-66541456	HCT-116	colon:	n/a	n/a
48	CTCF	chr13:66559941-66559944	NHEK	skin:	n/a	n/a
49	CTCF	chr13:66541140-66541290	HAc	cerebellar:	n/a	n/a
50	CTCF	chr13:66541180-66541330	HEK293	kidney:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:66583686-66583736	HEEpiC	esophagus:	n/a
2	chr13:66583583-66583633	NHDF-neo	bronchial:	n/a
3	chr13:66583686-66583736	AG10803	skin:	n/a
4	chr13:66583686-66583736	NH-A	brain:	n/a
5	chr13:66607275-66607325	CMK	blood:	n/a
6	chr13:66607275-66607325	Hepatocyte	liver:	n/a
7	chr13:66583686-66583736	MCF-7	breast:	n/a
8	chr13:66583583-66583633	NH-A	brain:	n/a
9	chr13:66607275-66607325	H1-hESC	embryonic stem cell:	embryo
10	chr13:66583686-66583736	PrEC	prostate:	n/a
11	chr13:66583583-66583633	HCT-116	colon:	n/a
12	chr13:66583686-66583736	PANC-1	pancreas:	n/a
13	chr13:66583583-66583633	SAEC	small airway:	n/a
14	chr13:66607275-66607325	HRE	kidney:	n/a
15	chr13:66583583-66583633	SK-N-SH_RA	brain:	n/a
16	chr13:66607275-66607325	SK-N-MC	brain:	n/a
17	chr13:66583583-66583633	Caco-2	colon:	n/a
18	chr13:66583583-66583633	HEK293	kidney:	embryo
19	chr13:66583686-66583736	GM12891	blood:	n/a
20	chr13:66607275-66607325	GM12892	blood:	n/a
21	chr13:66583686-66583736	HCT-116	colon:	n/a
22	chr13:66607275-66607325	HIPEpiC	eye:	n/a
23	chr13:66583583-66583633	PrEC	prostate:	n/a
24	chr13:66607275-66607325	HepG2	liver:	n/a
25	chr13:66583686-66583736	NB4	blood:	n/a
26	chr13:66583583-66583633	HEEpiC	esophagus:	n/a
27	chr13:66583686-66583736	PFSK-1	brain:	n/a
28	chr13:66607275-66607325	AG10803	skin:	n/a
29	chr13:66583686-66583736	HRCEpiC	kidney:	n/a
30	chr13:66607275-66607325	Caco-2	colon:	n/a
31	chr13:66583583-66583633	A549	lung:	n/a
32	chr13:66583583-66583633	PANC-1	pancreas:	n/a
33	chr13:66583686-66583736	U87	brain:	n/a
34	chr13:66583686-66583736	HPAEpiC	pulmonary alveolar:	n/a
35	chr13:66583686-66583736	CMK	blood:	n/a
36	chr13:66583686-66583736	BE2_C	brain:	n/a
37	chr13:66583686-66583736	NHBE	bronchial:	n/a
38	chr13:66583686-66583736	AG04449	skin:	fetal
39	chr13:66583583-66583633	IMR90	lung:	fetal
40	chr13:66583686-66583736	ProgFib	skin:	n/a
41	chr13:66583583-66583633	HUVEC	blood vessel:	n/a
42	chr13:66583686-66583736	SKMC	muscle:	n/a
43	chr13:66583583-66583633	Hela-S3	cervix:	n/a
44	chr13:66583583-66583633	GM19239	blood:	n/a
45	chr13:66583583-66583633	GM06990	blood:	n/a
46	chr13:66583583-66583633	HMEC	breast:	n/a
47	chr13:66583686-66583736	ECC-1	luminal epithelium:	n/a
48	chr13:66583583-66583633	PFSK-1	brain:	n/a
49	chr13:66583583-66583633	MCF10A-Er-Src	breast:	n/a
50	chr13:66583583-66583633	BE2_C	brain:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:66582815..66585533-chr13:66632919..66634778,2	K562	blood:
2	chr13:66557440..66557967-chr13:82054818..82055319,2	MCF-7	breast:
3	chr13:66606276..66609107-chr13:66609295..66610970,2	MCF-7	breast:
4	chr12:28240626..28241152-chr13:66662383..66662898,2	MCF-7	breast:
5	chr13:66582815..66585533-chr13:66632919..66634778,2	K562	blood:
6	chr13:66606276..66609107-chr13:66609295..66610970,2	MCF-7	breast:
7	chr13:66622814..66624893-chr13:66627297..66630041,2	K562	blood:
8	chr13:66500564..66501578-chr13:66540848..66541721,3	MCF-7	breast:
9	chr13:66230680..66231446-chr13:66540896..66541772,3	MCF-7	breast:
10	chr13:66622814..66624893-chr13:66627297..66630041,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL445989.1-10	chr13:66546596-66551943	XLOC_010415
2	lnc-AL445989.1-11	chr13:66628093-66628119	XLOC_010416
3	lnc-AL445989.1-11	chr13:66569993-66570140	XLOC_010416
4	lnc-AL445989.1-11	chr13:66569686-66569896	XLOC_010416

miRNA name	Chromosome Location	mirBase accession
hsa-miR-548x-3p	chr13:66540484-66540503	MIMAT0015081

No data

Variant related genes	Relation type
MIR548X2	TF binding region
MIR548X2	CpG island
INO80D	miRNA target sites

Extended variants
information (count: 2452 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:2452 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186329204	chr13:66517174-66517175	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs541066514	chr13:66517289-66517290	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs78076748	chr13:66517297-66517298	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs142323292	chr13:66517330-66517331	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs544058496	chr13:66517423-66517424	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs563845422	chr13:66517463-66517464	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs144613311	chr13:66517473-66517474	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs541861663	chr13:66517552-66517553	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs561624688	chr13:66517569-66517570	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs148209848	chr13:66517577-66517578	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs546972157	chr13:66517586-66517587	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs570692321	chr13:66517599-66517600	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs191124055	chr13:66517613-66517614	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs533026790	chr13:66517697-66517698	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs9529002	chr13:66517758-66517759	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs141204505	chr13:66517787-66517788	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs535583073	chr13:66517843-66517844	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs183506226	chr13:66517872-66517873	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs549825861	chr13:66517873-66517874	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs12870165	chr13:66517926-66517927	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs186034965	chr13:66517940-66517941	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs190797957	chr13:66517941-66517942	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs117542913	chr13:66517942-66517943	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs578255617	chr13:66518004-66518005	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs183262917	chr13:66518096-66518097	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs557591395	chr13:66518165-66518166	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs139333139	chr13:66518175-66518176	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs574220858	chr13:66518184-66518185	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs542842922	chr13:66518191-66518192	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs565731796	chr13:66518237-66518238	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs187989457	chr13:66518297-66518298	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs561853696	chr13:66518308-66518309	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs572023843	chr13:66518321-66518322	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs17252214	chr13:66518340-66518341	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs563701571	chr13:66518401-66518402	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs192552715	chr13:66518444-66518445	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs370764608	chr13:66518478-66518479	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs537339013	chr13:66518499-66518500	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs539571743	chr13:66518584-66518585	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs529129293	chr13:66518587-66518588	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs182627548	chr13:66518632-66518633	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs556992562	chr13:66518676-66518677	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs1224196	chr13:66518743-66518744	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs142612571	chr13:66518785-66518786	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs150757394	chr13:66518812-66518813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs551814790	chr13:66518920-66518921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs571620991	chr13:66518933-66518934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs576359324	chr13:66518944-66518945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs118034599	chr13:66518954-66518955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs557726258	chr13:66518961-66518962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	17245344	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Merkel cell carcinoma	19020549	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21858162	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Colorectal cancer	16774939	CNVD
Adenoid cystic carcinoma	17372589	CNVD
abnormal development	18461090	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Prostate cancer	16461572	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Intellectual disability	21811512	CNVD
Colorectal cancer	21645411	CNVD
Melanoma	20877625	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	20967226	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:106 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:66514600-66517400	Weak transcription	Colon Smooth Muscle	Colon
2	chr13:66515200-66517400	Weak transcription	Fetal Heart	heart
3	chr13:66515800-66517800	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr13:66516800-66517800	Enhancers	HUVEC	blood vessel
5	chr13:66516800-66518200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr13:66516800-66531000	Weak transcription	Left Ventricle	heart
7	chr13:66517000-66518400	Enhancers	Muscle Satellite Cultured Cells	--
8	chr13:66517200-66518000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr13:66517200-66518000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr13:66517200-66518600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr13:66517400-66518000	Enhancers	Osteobl	bone
12	chr13:66517400-66518200	Enhancers	Colon Smooth Muscle	Colon
13	chr13:66517400-66518200	Enhancers	Fetal Heart	heart
14	chr13:66517800-66518200	Flanking Active TSS	HUVEC	blood vessel
15	chr13:66517800-66518800	Enhancers	Pancreatic Islets	Pancreatic Islet
16	chr13:66518200-66518800	Enhancers	HUVEC	blood vessel
17	chr13:66520600-66520800	Enhancers	HUVEC	blood vessel
18	chr13:66531000-66531400	Enhancers	Left Ventricle	heart
19	chr13:66533000-66533800	Enhancers	HMEC	breast
20	chr13:66533200-66537400	Weak transcription	Aorta	Aorta
21	chr13:66533800-66538600	Weak transcription	HMEC	breast
22	chr13:66537400-66537600	ZNF genes & repeats	Aorta	Aorta
23	chr13:66537600-66538000	Weak transcription	Aorta	Aorta
24	chr13:66538600-66539000	Enhancers	HMEC	breast
25	chr13:66538800-66539200	Enhancers	Muscle Satellite Cultured Cells	--
26	chr13:66538800-66539800	Enhancers	NHDF-Ad	bronchial
27	chr13:66538800-66540600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr13:66539600-66540200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr13:66540200-66541200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr13:66540600-66541000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr13:66541000-66541800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr13:66541200-66542000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr13:66545000-66545600	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr13:66545000-66546000	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr13:66545000-66546000	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr13:66545000-66546000	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr13:66545200-66546000	Enhancers	H1 Cell Line	embryonic stem cell
38	chr13:66545400-66545800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr13:66545400-66546000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr13:66545400-66546000	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr13:66545600-66546000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr13:66546400-66547000	Enhancers	Aorta	Aorta
43	chr13:66551800-66552000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr13:66559600-66559800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr13:66562400-66562600	Enhancers	Left Ventricle	heart
46	chr13:66566400-66566800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr13:66575000-66575600	Enhancers	Pancreatic Islets	Pancreatic Islet
48	chr13:66575200-66575600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr13:66584800-66587400	Active TSS	K562	blood
50	chr13:66605800-66608600	Enhancers	HUES48 Cell Line	embryonic stem cell

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