Variant report

Variant	nsv515785
Chromosome Location	chr10:54981512-55093531
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:306)
CpG islands
(count:123)
Chromatin interactive
region (count:8)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr10:54999946-54999953	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr10:55025742-55025775	K562	blood:	n/a	n/a
3	BRCA1	chr10:55040336-55040499	GM12878	blood:	n/a	n/a
4	CEBPB	chr10:55054100-55054129	K562	blood:	n/a	n/a
5	CEBPB	chr10:55030432-55030743	HepG2	liver:	n/a	chr10:55030581-55030592
6	CEBPB	chr10:55030463-55030602	H1-hESC	embryonic stem cell:	n/a	chr10:55030581-55030592
7	CEBPB	chr10:55030423-55030723	A549	lung:	n/a	chr10:55030581-55030592
8	CEBPB	chr10:55063815-55064038	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr10:55070715-55071009	IMR90	lung:	n/a	chr10:55070859-55070872 chr10:55070861-55070870 chr10:55070861-55070870 chr10:55070861-55070870
10	CEBPB	chr10:55016346-55017038	Hela-S3	cervix:	n/a	chr10:55016409-55016420
11	CEBPB	chr10:55063709-55063996	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr10:55070800-55070915	H1-hESC	embryonic stem cell:	n/a	chr10:55070859-55070872 chr10:55070861-55070870 chr10:55070861-55070870 chr10:55070861-55070870
13	CEBPB	chr10:55063721-55064073	IMR90	lung:	n/a	n/a
14	CEBPB	chr10:55074637-55075013	IMR90	lung:	n/a	n/a
15	CEBPB	chr10:55030411-55030719	IMR90	lung:	n/a	chr10:55030581-55030592
16	CEBPB	chr10:55063756-55064049	A549	lung:	n/a	n/a
17	CEBPB	chr10:55063725-55064069	HepG2	liver:	n/a	n/a
18	CEBPB	chr10:55016353-55016995	H1-hESC	embryonic stem cell:	n/a	chr10:55016409-55016420
19	CEBPB	chr10:55030433-55030717	Hela-S3	cervix:	n/a	chr10:55030581-55030592
20	CEBPB	chr10:55077103-55077366	H1-hESC	embryonic stem cell:	n/a	chr10:55077105-55077118 chr10:55077104-55077121
21	CEBPB	chr10:55016818-55017080	HepG2	liver:	n/a	n/a
22	CTCF	chr10:55031520-55031670	HEK293	kidney:	n/a	n/a
23	CTCF	chr10:55075589-55075808	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr10:55075556-55075788	HUVEC	blood vessel:	n/a	n/a
25	CTCF	chr10:55016640-55016790	HMEC	breast:	n/a	n/a
26	CTCF	chr10:55058280-55058430	GM12866	blood:	n/a	n/a
27	CTCF	chr10:55075580-55075730	HRE	kidney:	n/a	n/a
28	CTCF	chr10:55058380-55058530	NHEK	skin:	n/a	n/a
29	CTCF	chr10:54981920-54981966	GM10248	blood:	n/a	n/a
30	CTCF	chr10:55058352-55058401	LNCaP	prostate:	n/a	n/a
31	CTCF	chr10:55080900-55081050	HRE	kidney:	n/a	n/a
32	CTCF	chr10:55058185-55058557	MCF-7	breast:	n/a	n/a
33	CTCF	chr10:55058240-55058390	SAEC	small airway:	n/a	n/a
34	CTCF	chr10:55058320-55058470	AG04449	skin:	n/a	n/a
35	CTCF	chr10:55058304-55058475	HUVEC	blood vessel:	n/a	n/a
36	CTCF	chr10:55058340-55058490	MCF-7	breast:	n/a	n/a
37	CTCF	chr10:55058320-55058470	HPAF	blood vessel:	n/a	n/a
38	CTCF	chr10:55031440-55031590	RPTEC	kidney:	n/a	n/a
39	CTCF	chr10:55081204-55081221	GM20000	blood:	n/a	n/a
40	CTCF	chr10:55075529-55075845	GM12878	blood:	n/a	n/a
41	CTCF	chr10:55075595-55075789	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr10:54983920-54984070	GM12868	blood:	n/a	n/a
43	CTCF	chr10:54986984-54987052	GM20000	blood:	n/a	n/a
44	CTCF	chr10:55075578-55075753	LNCaP	prostate:	n/a	n/a
45	CTCF	chr10:55058380-55058530	HEK293	kidney:	n/a	n/a
46	CTCF	chr10:55075600-55075750	HRE	kidney:	n/a	n/a
47	CTCF	chr10:55075600-55075750	NHEK	skin:	n/a	n/a
48	CTCF	chr10:55031420-55031570	MCF-7	breast:	n/a	n/a
49	CTCF	chr10:55075600-55075724	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr10:55058340-55058490	HEEpiC	esophagus:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:55016939-55016989	T-47D	breast:	n/a
2	chr10:55016939-55016989	T-47D	breast:	n/a
3	chr10:54984564-54984614	SK-N-SH	brain:	n/a
4	chr10:54984564-54984614	AG10803	skin:	n/a
5	chr10:54984564-54984614	SK-N-SH_RA	brain:	n/a
6	chr10:55016939-55016989	GM19239	blood:	n/a
7	chr10:55016939-55016989	NH-A	brain:	n/a
8	chr10:54984564-54984614	NHBE	bronchial:	n/a
9	chr10:54984564-54984614	HPAEpiC	pulmonary alveolar:	n/a
10	chr10:55016939-55016989	U87	brain:	n/a
11	chr10:55016939-55016989	HPAEpiC	pulmonary alveolar:	n/a
12	chr10:55016939-55016989	NT2-D1	testis:	n/a
13	chr10:54984564-54984614	LNCaP	prostate:	n/a
14	chr10:54984564-54984614	NT2-D1	testis:	n/a
15	chr10:54984564-54984614	ECC-1	luminal epithelium:	n/a
16	chr10:54984564-54984614	RPTEC	kidney:	n/a
17	chr10:55016939-55016989	SKMC	muscle:	n/a
18	chr10:55016939-55016989	HRE	kidney:	n/a
19	chr10:55016939-55016989	HepG2	liver:	n/a
20	chr10:55016939-55016989	BE2_C	brain:	n/a
21	chr10:54984564-54984614	GM12891	blood:	n/a
22	chr10:55016939-55016989	PFSK-1	brain:	n/a
23	chr10:55016939-55016989	IMR90	lung:	fetal
24	chr10:55016939-55016989	ECC-1	luminal epithelium:	n/a
25	chr10:54984564-54984614	Hela-S3	cervix:	n/a
26	chr10:54984564-54984614	AoSMC	blood vessel:	n/a
27	chr10:55016939-55016989	LNCaP	prostate:	n/a
28	chr10:55016939-55016989	AoSMC	blood vessel:	n/a
29	chr10:54984564-54984614	HRCEpiC	kidney:	n/a
30	chr10:54984564-54984614	HIPEpiC	eye:	n/a
31	chr10:54984564-54984614	PFSK-1	brain:	n/a
32	chr10:55016939-55016989	H1-hESC	embryonic stem cell:	embryo
33	chr10:55016939-55016989	K562	blood:	n/a
34	chr10:55016939-55016989	SK-N-MC	brain:	n/a
35	chr10:54984564-54984614	GM19239	blood:	n/a
36	chr10:54984564-54984614	HAEpiC	amniotic membrane:	n/a
37	chr10:55016939-55016989	HCPEpiC	choroid plexus:	n/a
38	chr10:55016939-55016989	NHDF-neo	bronchial:	n/a
39	chr10:54984564-54984614	HL-60	blood:	n/a
40	chr10:54984564-54984614	A549	lung:	n/a
41	chr10:54984564-54984614	HCM	heart:	n/a
42	chr10:54984564-54984614	CMK	blood:	n/a
43	chr10:55016939-55016989	GM12891	blood:	n/a
44	chr10:55016939-55016989	Jurkat	blood:	n/a
45	chr10:55016939-55016989	AG09309	skin:	n/a
46	chr10:55016939-55016989	Hepatocyte	liver:	n/a
47	chr10:54984564-54984614	SAEC	small airway:	n/a
48	chr10:54984564-54984614	HepG2	liver:	n/a
49	chr10:55016939-55016989	CMK	blood:	n/a
50	chr10:54984564-54984614	U87	brain:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:55015124..55017354-chr10:55018929..55021209,2	K562	blood:
2	chr10:55028156..55030475-chr10:55032367..55034713,2	K562	blood:
3	chr10:55010159..55011051-chr10:101190203..101191138,2	Hela-S3	cervix:
4	chr10:55028156..55030475-chr10:55032367..55034713,2	K562	blood:
5	chr10:55015124..55017354-chr10:55018929..55021209,2	K562	blood:
6	chr10:55057963..55058535-chr10:55568196..55569129,2	MCF-7	breast:
7	chr10:55028397..55030475-chr10:55031728..55034713,2	K562	blood:
8	chr10:55028397..55030475-chr10:55031728..55034713,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCDH15-1	chr10:55070752-55070825	XLOC_008827
2	lnc-PCDH15-1	chr10:55050832-55051354	XLOC_008827

No data

Variant related genes	Relation type
ENSG00000226296	TF binding region
ENSG00000226296	CpG island
ENSG00000224934	chromatin interactions
ENSG00000120053	chromatin interactions

Extended variants
information (count: 3217 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:3217 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1903933	chr10:54981512-54981513	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs547729257	chr10:54981563-54981564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs559629939	chr10:54981565-54981566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs528288828	chr10:54981589-54981590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs150795337	chr10:54981603-54981604	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs571372945	chr10:54981637-54981638	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs139055228	chr10:54981647-54981648	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs369998992	chr10:54981649-54981650	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs1903932	chr10:54981652-54981653	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs567128259	chr10:54981674-54981675	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs536986739	chr10:54981740-54981741	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs114379059	chr10:54981833-54981834	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs187615663	chr10:54981841-54981842	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs1903931	chr10:54981860-54981861	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs368202784	chr10:54981872-54981873	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs558693271	chr10:54981878-54981879	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs575357644	chr10:54981884-54981885	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs544359139	chr10:54981900-54981901	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs113216198	chr10:54981901-54981902	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs375649680	chr10:54981902-54981903	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs574734519	chr10:54981923-54981924	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs542958698	chr10:54981938-54981939	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs189090353	chr10:54981945-54981946	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs528351968	chr10:54982006-54982007	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs373337744	chr10:54982014-54982015	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs565043762	chr10:54982031-54982032	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs529983716	chr10:54982032-54982033	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs376764345	chr10:54982035-54982036	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs181021053	chr10:54982049-54982050	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs375460560	chr10:54982050-54982051	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs11003465	chr10:54982056-54982057	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs12415405	chr10:54982072-54982073	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs567294692	chr10:54982105-54982106	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs529660677	chr10:54982157-54982158	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs529132185	chr10:54982171-54982172	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs566840053	chr10:54982177-54982178	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs538919113	chr10:54982179-54982180	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs11003466	chr10:54982181-54982182	Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs569338764	chr10:54982199-54982200	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs569041077	chr10:54982244-54982245	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs537963831	chr10:54982266-54982267	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs78620231	chr10:54982282-54982283	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs61862162	chr10:54982291-54982292	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs138939758	chr10:54982340-54982341	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs554765570	chr10:54982354-54982355	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs574825998	chr10:54982395-54982396	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs149453575	chr10:54982470-54982471	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs554172650	chr10:54982551-54982552	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs573195593	chr10:54982552-54982553	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs111561972	chr10:54982564-54982565	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Obesity	21956041	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Intellectual disability	21948486	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16272173	CNVD
Metanephric adenoma	20802469	CNVD
Autism	20841430	CNVD
Mental retardation	17124404	CNVD
Epilepsy	20923578	CNVD
Prostate cancer	16573809	CNVD
Schizophrenia	19329560	CNVD
Heart failure	18772530	CNVD
Heart failure	18854381	CNVD
Hyperglycemia	19060297	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Glioblastoma multiforme	22286061	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Usher syndrome	20538994	CNVD
Glioblastoma multiforme	17002787	CNVD
Colorectal cancer	16774939	CNVD
Autism	20858243	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:190 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:54966400-54981600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr10:54981600-54983200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr10:54981600-54983200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
4	chr10:54982000-54984000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr10:54982200-54982400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
6	chr10:54983000-54983200	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr10:54983000-54983400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
8	chr10:54983200-54984200	Enhancers	Fetal Muscle Leg	muscle
9	chr10:54983200-54984400	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr10:54983200-54984600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr10:54983200-54984600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr10:54983200-54984800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr10:54983400-54984000	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr10:54983400-54984200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr10:54983400-54984800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr10:54983400-54985600	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr10:54983400-54985600	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr10:54983600-54984000	Enhancers	H9 Cell Line	embryonic stem cell
19	chr10:54983600-54984200	Enhancers	H1 Cell Line	embryonic stem cell
20	chr10:54983600-54984200	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr10:54983600-54984200	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr10:54983600-54984200	Enhancers	Fetal Lung	lung
23	chr10:54983600-54985600	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr10:54983800-54984200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr10:54983800-54984200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr10:54984000-54984400	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr10:54984000-54984600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr10:54984200-54984400	Enhancers	Fetal Stomach	stomach
29	chr10:54984200-54985200	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr10:54984200-54985200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr10:54984200-54985400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr10:54984400-54985600	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr10:54984600-54984800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr10:54984600-54984800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr10:54984600-54985200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr10:54985200-54985400	Enhancers	H1 Cell Line	embryonic stem cell
37	chr10:54985200-54985600	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr10:54985200-55005200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr10:54985400-54985600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr10:54991600-54991800	Enhancers	Fetal Heart	heart
41	chr10:54991800-54992200	Flanking Active TSS	Fetal Heart	heart
42	chr10:54992200-54994000	Enhancers	Fetal Heart	heart
43	chr10:54993200-54994000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr10:54993400-54993800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr10:54993600-54994000	Enhancers	Fetal Lung	lung
46	chr10:54993600-54994600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr10:54996400-54996800	Enhancers	Fetal Intestine Small	intestine
48	chr10:54996600-54997400	Enhancers	Rectal Mucosa Donor 31	rectum
49	chr10:55003200-55004000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr10:55005200-55006200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links