Variant report

Variant	nsv1044535
Chromosome Location	chr10:4271872-4306421
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:502)
CpG islands
(count:61)
Chromatin interactive
region (count:15)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:502 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr10:4296957-4297180	K562	blood:	n/a	n/a
2	ATF1	chr10:4276937-4277258	K562	blood:	n/a	n/a
3	ATF1	chr10:4304785-4304985	K562	blood:	n/a	n/a
4	ATF3	chr10:4276995-4277163	K562	blood:	n/a	n/a
5	BCL3	chr10:4304705-4304906	GM12878	blood:	n/a	n/a
6	BCL3	chr10:4304633-4304899	GM12878	blood:	n/a	n/a
7	CBX3	chr10:4285844-4286362	HCT-116	colon:	n/a	n/a
8	CBX3	chr10:4302647-4303081	HCT-116	colon:	n/a	n/a
9	CBX3	chr10:4275040-4275358	HCT-116	colon:	n/a	n/a
10	CCNT2	chr10:4276995-4277195	K562	blood:	n/a	n/a
11	CEBPB	chr10:4305189-4305928	Hela-S3	cervix:	n/a	chr10:4305239-4305250
12	CEBPB	chr10:4305612-4305739	IMR90	lung:	n/a	n/a
13	CEBPB	chr10:4274097-4274100	A549	lung:	n/a	n/a
14	CEBPB	chr10:4284615-4285259	HCT-116	colon:	n/a	n/a
15	CEBPB	chr10:4282853-4283500	IMR90	lung:	n/a	n/a
16	CEBPB	chr10:4276922-4277122	HepG2	liver:	n/a	chr10:4277009-4277020
17	CEBPB	chr10:4296810-4297453	IMR90	lung:	n/a	n/a
18	CEBPB	chr10:4285751-4286264	IMR90	lung:	n/a	n/a
19	CEBPB	chr10:4296845-4297267	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr10:4276867-4277127	A549	lung:	n/a	chr10:4277009-4277020
21	CEBPB	chr10:4292740-4292819	HepG2	liver:	n/a	chr10:4292773-4292784
22	CEBPB	chr10:4276851-4277288	MCF-7	breast:	n/a	chr10:4277009-4277020
23	CEBPB	chr10:4276851-4277242	K562	blood:	n/a	chr10:4277009-4277020
24	CEBPB	chr10:4285804-4286368	HCT-116	colon:	n/a	n/a
25	CEBPB	chr10:4282886-4283178	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr10:4296947-4297179	A549	lung:	n/a	n/a
27	CEBPB	chr10:4285878-4286272	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr10:4284358-4285073	Hela-S3	cervix:	n/a	chr10:4284406-4284417
29	CEBPB	chr10:4284004-4284995	IMR90	lung:	n/a	chr10:4284406-4284417
30	CEBPB	chr10:4288948-4289680	IMR90	lung:	n/a	n/a
31	CTCF	chr10:4276980-4277130	HCT-116	colon:	n/a	n/a
32	CTCF	chr10:4288900-4289050	HCFaa	heart:	n/a	n/a
33	CTCF	chr10:4288960-4289110	AoAF	blood vessel:	n/a	n/a
34	CTCF	chr10:4276949-4277227	K562	blood:	n/a	n/a
35	CTCF	chr10:4276920-4277070	HVMF	connective:	n/a	n/a
36	CTCF	chr10:4290826-4290944	GM19238	blood:	n/a	chr10:4290882-4290903
37	CTCF	chr10:4277000-4277150	A549	lung:	n/a	n/a
38	CTCF	chr10:4284820-4284970	HCPEpiC	choroid plexus:	n/a	n/a
39	CTCF	chr10:4276940-4277090	HEK293	kidney:	n/a	n/a
40	CTCF	chr10:4276980-4277130	GM12872	blood:	n/a	n/a
41	CTCF	chr10:4284760-4284910	AG10803	skin:	n/a	n/a
42	CTCF	chr10:4288940-4289090	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr10:4277005-4277156	K562	blood:	n/a	n/a
44	CTCF	chr10:4300325-4300371	A549	lung:	n/a	n/a
45	CTCF	chr10:4277000-4277150	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr10:4277020-4277170	HPF	lung:	n/a	n/a
47	CTCF	chr10:4300340-4300490	HepG2	liver:	n/a	n/a
48	CTCF	chr10:4276980-4277130	HL-60	blood:	n/a	n/a
49	CTCF	chr10:4288940-4289090	AG10803	skin:	n/a	n/a
50	CTCF	chr10:4277029-4277094	Hela-S3	cervix:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:4296406-4296456	BJ	skin:	n/a
2	chr10:4296406-4296456	HAEpiC	amniotic membrane:	n/a
3	chr10:4296406-4296456	HMEC	breast:	n/a
4	chr10:4296406-4296456	Hepatocyte	liver:	n/a
5	chr10:4296406-4296456	HCM	heart:	n/a
6	chr10:4296406-4296456	IMR90	lung:	fetal
7	chr10:4296406-4296456	HCT-116	colon:	n/a
8	chr10:4296406-4296456	H1-hESC	embryonic stem cell:	embryo
9	chr10:4296406-4296456	HUVEC	blood vessel:	n/a
10	chr10:4296406-4296456	SK-N-SH_RA	brain:	n/a
11	chr10:4296406-4296456	HCF	heart:	n/a
12	chr10:4296406-4296456	HCPEpiC	choroid plexus:	n/a
13	chr10:4296406-4296456	GM12891	blood:	n/a
14	chr10:4296406-4296456	K562	blood:	n/a
15	chr10:4296406-4296456	NT2-D1	testis:	n/a
16	chr10:4296406-4296456	NB4	blood:	n/a
17	chr10:4296406-4296456	GM19239	blood:	n/a
18	chr10:4296406-4296456	Hela-S3	cervix:	n/a
19	chr10:4296406-4296456	ProgFib	skin:	n/a
20	chr10:4296406-4296456	HPAEpiC	pulmonary alveolar:	n/a
21	chr10:4296406-4296456	HIPEpiC	eye:	n/a
22	chr10:4296406-4296456	HL-60	blood:	n/a
23	chr10:4296406-4296456	AG09309	skin:	n/a
24	chr10:4296406-4296456	AG10803	skin:	n/a
25	chr10:4296406-4296456	AG04450	lung:	fetal
26	chr10:4296406-4296456	GM12892	blood:	n/a
27	chr10:4296406-4296456	Caco-2	colon:	n/a
28	chr10:4296406-4296456	PrEC	prostate:	n/a
29	chr10:4296406-4296456	AG04449	skin:	fetal
30	chr10:4296406-4296456	GM06990	blood:	n/a
31	chr10:4296406-4296456	NHBE	bronchial:	n/a
32	chr10:4296406-4296456	ovcar-3	ovarian:	n/a
33	chr10:4296406-4296456	AoSMC	blood vessel:	n/a
34	chr10:4296406-4296456	T-47D	breast:	n/a
35	chr10:4296406-4296456	SK-N-MC	brain:	n/a
36	chr10:4296406-4296456	GM12878	blood:	n/a
37	chr10:4296406-4296456	SAEC	small airway:	n/a
38	chr10:4296406-4296456	SKMC	muscle:	n/a
39	chr10:4296406-4296456	SK-N-SH	brain:	n/a
40	chr10:4296406-4296456	HRE	kidney:	n/a
41	chr10:4296406-4296456	ECC-1	luminal epithelium:	n/a
42	chr10:4296406-4296456	HNPCEpiC	eye:	n/a
43	chr10:4296406-4296456	LNCaP	prostate:	n/a
44	chr10:4296406-4296456	HEK293	kidney:	embryo
45	chr10:4296406-4296456	NH-A	brain:	n/a
46	chr10:4296406-4296456	RPTEC	kidney:	n/a
47	chr10:4296406-4296456	HEEpiC	esophagus:	n/a
48	chr10:4296406-4296456	AG09319	gingival:	n/a
49	chr10:4296406-4296456	CMK	blood:	n/a
50	chr10:4296406-4296456	MCF10A-Er-Src	breast:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:4304386..4306768-chr10:4318241..4320361,3	MCF-7	breast:
2	chr10:3824875..3826995-chr10:4293449..4295482,2	MCF-7	breast:
3	chr10:4243895..4246337-chr10:4299306..4301962,2	MCF-7	breast:
4	chr10:4280040..4281988-chr10:4283638..4285219,2	MCF-7	breast:
5	chr10:3823986..3829739-chr10:4306109..4310504,8	MCF-7	breast:
6	chr10:3825342..3830573-chr10:4304925..4310190,7	MCF-7	breast:
7	chr10:4301639..4303870-chr10:4304089..4305971,2	MCF-7	breast:
8	chr10:4278158..4281099-chr10:4281519..4283245,2	MCF-7	breast:
9	chr10:4301639..4303870-chr10:4304089..4305971,2	MCF-7	breast:
10	chr10:4280040..4281988-chr10:4283638..4285219,2	MCF-7	breast:
11	chr10:4278158..4281099-chr10:4281519..4283245,2	MCF-7	breast:
12	chr10:3826852..3829310-chr10:4280995..4283154,3	MCF-7	breast:
13	chr10:3826008..3828712-chr10:4299777..4301639,2	MCF-7	breast:
14	chr10:4275653..4277576-chr10:4279450..4282362,2	K562	blood:
15	chr10:4275653..4277576-chr10:4279450..4282362,2	K562	blood:

(count:23 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KLF6-7	chr10:4285696-4285835	XLOC_008700
2	lnc-KLF6-6	chr10:4275696-4276007	l_239_chr10:4233289-4275926_adrenal
3	lnc-KLF6-7	chr10:4286015-4286104	ENSG00000233117.2
4	lnc-KLF6-7	chr10:4285142-4285301	XLOC_008700
5	lnc-KLF6-14	chr10:4284529-4284775	NONHSAT011085
6	lnc-KLF6-7	chr10:4285696-4285957	XLOC_008700
7	lnc-KLF6-6	chr10:4276015-4276038	l_239_chr10:4233289-4275926_adrenal
8	lnc-KLF6-7	chr10:4277491-4277974	NONHSAT011084
9	lnc-KLF6-7	chr10:4286015-4286104	NR_108040
10	lnc-KLF6-6	chr10:4273551-4275038	l_239_chr10:4233289-4275926_adrenal
11	lnc-KLF6-6	chr10:4275142-4275301	NONHSAT011083
12	lnc-KLF6-14	chr10:4284539-4284771	NONHSAT011086
13	lnc-KLF6-6	chr10:4275696-4275835	NONHSAT011082
14	lnc-KLF6-7	chr10:4285696-4285981	XLOC_008700
15	lnc-KLF6-6	chr10:4275696-4275981	NONHSAT011083
16	lnc-KLF6-7	chr10:4277752-4277974	XLOC_008700
17	lnc-KLF6-7	chr10:4285696-4285879	NR_108040
18	lnc-KLF6-7	chr10:4285696-4285728	NONHSAT011084
19	lnc-KLF6-6	chr10:4275042-4275301	l_239_chr10:4233289-4275926_adrenal
20	lnc-KLF6-6	chr10:4282814-4283144	XLOC_008701
21	lnc-KLF6-7	chr10:4285696-4285879	ENSG00000233117.2
22	lnc-KLF6-6	chr10:4275330-4275363	l_239_chr10:4233289-4275926_adrenal
23	lnc-KLF6-6	chr10:4273221-4273285	l_239_chr10:4233289-4275926_adrenal

No data

Variant related genes	Relation type
LINC00702	TF binding region
LINC00702	CpG island
ENSG00000067082	chromatin interactions

Extended variants
information (count: 1603 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1603 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10437533	chr10:4271872-4271873	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs147163389	chr10:4271910-4271911	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs542052342	chr10:4271953-4271954	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs144653537	chr10:4271955-4271956	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs372284574	chr10:4271956-4271957	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs10437534	chr10:4271996-4271997	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs575489891	chr10:4272003-4272004	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs116226892	chr10:4272020-4272021	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs374899276	chr10:4272029-4272030	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs542513415	chr10:4272062-4272063	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs561335193	chr10:4272068-4272069	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs531604616	chr10:4272091-4272092	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs115087351	chr10:4272100-4272101	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs565217286	chr10:4272120-4272121	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs369329777	chr10:4272140-4272141	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs532781170	chr10:4272172-4272173	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs377693694	chr10:4272187-4272188	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs11380834	chr10:4272199-4272200	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs548032812	chr10:4272225-4272226	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs566244148	chr10:4272255-4272256	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs530427118	chr10:4272260-4272261	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs7907379	chr10:4272271-4272272	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567303133	chr10:4272279-4272280	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs546075599	chr10:4272305-4272306	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs189345823	chr10:4272332-4272333	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs556259857	chr10:4272341-4272342	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs570990331	chr10:4272354-4272355	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs180887048	chr10:4272375-4272376	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs553558635	chr10:4272376-4272377	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs571859261	chr10:4272380-4272381	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs542954696	chr10:4272397-4272398	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs554557649	chr10:4272407-4272408	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs576416212	chr10:4272409-4272410	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs371287274	chr10:4272462-4272463	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs140355158	chr10:4272516-4272517	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs532670408	chr10:4272524-4272525	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs541497758	chr10:4272526-4272527	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs142167352	chr10:4272527-4272528	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs530315924	chr10:4272528-4272529	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs548907873	chr10:4272590-4272591	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs79005304	chr10:4272591-4272592	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs34639009	chr10:4272600-4272601	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs570238875	chr10:4272609-4272610	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs116725046	chr10:4272686-4272687	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs549524679	chr10:4272759-4272760	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs66764883	chr10:4272793-4272794	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs149199255	chr10:4272795-4272796	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs72138289	chr10:4272796-4272797	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs57448447	chr10:4272798-4272799	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs369004209	chr10:4272822-4272823	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Cancer	21129771	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	17363583	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	21611746	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:726 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:4257400-4282400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr10:4269400-4277400	Weak transcription	Aorta	Aorta
3	chr10:4271000-4272200	Enhancers	HMEC	breast
4	chr10:4271200-4272400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr10:4271400-4272200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr10:4271400-4272600	Enhancers	NHEK	skin
7	chr10:4271400-4273200	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr10:4271800-4272800	Enhancers	Colon Smooth Muscle	Colon
9	chr10:4271800-4273000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr10:4272400-4283200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr10:4272800-4275200	Weak transcription	Colon Smooth Muscle	Colon
12	chr10:4274600-4274800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
13	chr10:4275000-4275200	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
14	chr10:4275000-4277600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
15	chr10:4275200-4275400	ZNF genes & repeats	Colon Smooth Muscle	Colon
16	chr10:4275200-4282800	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr10:4275800-4276000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr10:4276000-4292200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr10:4276200-4278400	Enhancers	Primary T cells fromperipheralblood	blood
20	chr10:4276200-4279000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr10:4276200-4281400	Weak transcription	NHDF-Ad	bronchial
22	chr10:4276400-4281400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr10:4276600-4284000	Weak transcription	Left Ventricle	heart
24	chr10:4276800-4278200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
25	chr10:4276800-4278400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
26	chr10:4277400-4277800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
27	chr10:4277400-4278000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
28	chr10:4277400-4278000	Strong transcription	Aorta	Aorta
29	chr10:4277600-4278000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
30	chr10:4277600-4278400	Enhancers	Primary T killer memory cells from peripheral blood	blood
31	chr10:4278000-4280200	Weak transcription	Aorta	Aorta
32	chr10:4278400-4282800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr10:4279000-4279200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr10:4279200-4283200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr10:4280200-4280400	Enhancers	Placenta Amnion	Placenta Amnion
36	chr10:4280200-4280600	ZNF genes & repeats	Aorta	Aorta
37	chr10:4280200-4282400	Weak transcription	NH-A	brain
38	chr10:4280400-4280600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr10:4280400-4280600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr10:4280400-4280600	Enhancers	Right Atrium	heart
41	chr10:4280400-4281200	Enhancers	Stomach Smooth Muscle	stomach
42	chr10:4280600-4281200	Genic enhancers	Aorta	Aorta
43	chr10:4280600-4282400	Weak transcription	Placenta Amnion	Placenta Amnion
44	chr10:4280600-4282800	Weak transcription	Right Atrium	heart
45	chr10:4280600-4283200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr10:4281200-4282200	Weak transcription	Aorta	Aorta
47	chr10:4281200-4282800	Weak transcription	Stomach Smooth Muscle	stomach
48	chr10:4281400-4281600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr10:4281400-4282800	Enhancers	NHDF-Ad	bronchial
50	chr10:4281600-4282000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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