Variant report

Variant	esv3361397
Chromosome Location	chr7:150747444-150749992
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:134)
CpG islands
(count:244)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:134 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr7:150748078-150748452	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr7:150748136-150748501	HepG2	liver:	n/a	n/a
3	BHLHE40	chr7:150748195-150748506	GM12878	blood:	n/a	n/a
4	BRCA1	chr7:150748277-150748480	H1-hESC	embryonic stem cell:	n/a	n/a
5	CCNT2	chr7:150748316-150748487	K562	blood:	n/a	n/a
6	CEBPB	chr7:150748171-150748609	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr7:150748176-150748676	IMR90	lung:	n/a	n/a
8	CHD1	chr7:150748020-150748657	IMR90	lung:	n/a	n/a
9	CHD2	chr7:150748131-150748541	H1-hESC	embryonic stem cell:	n/a	n/a
10	CREB1	chr7:150747965-150748603	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr7:150748220-150748370	SAEC	small airway:	n/a	n/a
12	E2F6	chr7:150748010-150748603	H1-hESC	embryonic stem cell:	n/a	chr7:150748216-150748225
13	E2F6	chr7:150747835-150748619	H1-hESC	embryonic stem cell:	n/a	chr7:150748216-150748225
14	ELF1	chr7:150748172-150748495	K562	blood:	n/a	chr7:150748212-150748224
15	ELF1	chr7:150748090-150748573	GM12878	blood:	n/a	chr7:150748212-150748224
16	EP300	chr7:150748154-150748467	H1-hESC	embryonic stem cell:	n/a	n/a
17	GABPA	chr7:150747986-150748565	H1-hESC	embryonic stem cell:	n/a	chr7:150748219-150748228 chr7:150748068-150748077
18	GABPA	chr7:150748058-150748591	H1-hESC	embryonic stem cell:	n/a	chr7:150748219-150748228 chr7:150748068-150748077
19	GTF2F1	chr7:150748277-150748477	H1-hESC	embryonic stem cell:	n/a	n/a
20	HMGN3	chr7:150748134-150748556	K562	blood:	n/a	n/a
21	JUND	chr7:150748245-150748473	H1-hESC	embryonic stem cell:	n/a	chr7:150748416-150748425 chr7:150748420-150748429
22	JUND	chr7:150748140-150748450	H1-hESC	embryonic stem cell:	n/a	chr7:150748416-150748425 chr7:150748420-150748429
23	MAFK	chr7:150749991-150750170	HepG2	liver:	n/a	chr7:150750118-150750132 chr7:150750115-150750130 chr7:150750115-150750131 chr7:150750119-150750130 chr7:150750120-150750131 chr7:150750120-150750131
24	MAX	chr7:150747885-150748585	H1-hESC	embryonic stem cell:	n/a	n/a
25	MAX	chr7:150747970-150748589	ECC-1	luminal epithelium:	n/a	n/a
26	MAX	chr7:150748123-150748556	HepG2	liver:	n/a	n/a
27	MAX	chr7:150748125-150748560	NB4	blood:	n/a	n/a
28	MAX	chr7:150748246-150748416	HepG2	liver:	n/a	n/a
29	MAX	chr7:150747977-150748599	ECC-1	luminal epithelium:	n/a	n/a
30	MAX	chr7:150748110-150748515	HUVEC	blood vessel:	n/a	n/a
31	MAX	chr7:150747933-150748569	H1-hESC	embryonic stem cell:	n/a	n/a
32	MAX	chr7:150748109-150748505	H1-hESC	embryonic stem cell:	n/a	n/a
33	MAZ	chr7:150748053-150748775	IMR90	lung:	n/a	n/a
34	MXI1	chr7:150748251-150748379	GM12878	blood:	n/a	n/a
35	MXI1	chr7:150748100-150748517	H1-hESC	embryonic stem cell:	n/a	n/a
36	MXI1	chr7:150748186-150748461	HepG2	liver:	n/a	n/a
37	MXI1	chr7:150747336-150748663	IMR90	lung:	n/a	n/a
38	MYC	chr7:150748148-150748470	MCF10A-Er-Src	breast:	n/a	n/a
39	MYC	chr7:150748132-150748542	NB4	blood:	n/a	n/a
40	MYC	chr7:150748112-150748523	H1-hESC	embryonic stem cell:	n/a	n/a
41	MYC	chr7:150748175-150748459	HUVEC	blood vessel:	n/a	n/a
42	NFIC	chr7:150748052-150748557	ECC-1	luminal epithelium:	n/a	n/a
43	NRF1	chr7:150748255-150748477	H1-hESC	embryonic stem cell:	n/a	n/a
44	POLR2A	chr7:150748078-150748147	K562	blood:	n/a	n/a
45	POLR2A	chr7:150748036-150748473	HUVEC	blood vessel:	n/a	n/a
46	POLR2A	chr7:150749897-150749905	K562	blood:	n/a	n/a
47	POLR2A	chr7:150749110-150749141	K562	blood:	n/a	n/a
48	POLR2A	chr7:150748304-150748408	Hela-S3	cervix:	n/a	n/a
49	POLR2A	chr7:150748078-150748518	ECC-1	luminal epithelium:	n/a	n/a
50	POLR2A	chr7:150748464-150748623	ProgFib	skin:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:150748069-150748119	HUVEC	blood vessel:	n/a
2	chr7:150749758-150749808	CMK	blood:	n/a
3	chr7:150749758-150749808	NT2-D1	testis:	n/a
4	chr7:150748518-150748568	AoSMC	blood vessel:	n/a
5	chr7:150748518-150748568	HCT-116	colon:	n/a
6	chr7:150748069-150748119	A549	lung:	n/a
7	chr7:150749758-150749808	U87	brain:	n/a
8	chr7:150749758-150749808	MCF10A-Er-Src	breast:	n/a
9	chr7:150748284-150748334	AG09319	gingival:	n/a
10	chr7:150748518-150748568	BJ	skin:	n/a
11	chr7:150748069-150748119	HAEpiC	amniotic membrane:	n/a
12	chr7:150749758-150749808	K562	blood:	n/a
13	chr7:150748069-150748119	Hepatocyte	liver:	n/a
14	chr7:150748284-150748334	BJ	skin:	n/a
15	chr7:150749758-150749808	AG10803	skin:	n/a
16	chr7:150748518-150748568	PrEC	prostate:	n/a
17	chr7:150748069-150748119	AG09319	gingival:	n/a
18	chr7:150748284-150748334	PFSK-1	brain:	n/a
19	chr7:150749758-150749808	ProgFib	skin:	n/a
20	chr7:150749758-150749808	H1-hESC	embryonic stem cell:	embryo
21	chr7:150748518-150748568	Caco-2	colon:	n/a
22	chr7:150748284-150748334	HCPEpiC	choroid plexus:	n/a
23	chr7:150748518-150748568	AG04449	skin:	fetal
24	chr7:150749758-150749808	Caco-2	colon:	n/a
25	chr7:150749758-150749808	SKMC	muscle:	n/a
26	chr7:150748284-150748334	Jurkat	blood:	n/a
27	chr7:150749758-150749808	BJ	skin:	n/a
28	chr7:150748518-150748568	AG09309	skin:	n/a
29	chr7:150748284-150748334	SAEC	small airway:	n/a
30	chr7:150749758-150749808	HRPEpiC	eye:	n/a
31	chr7:150748284-150748334	HPAEpiC	pulmonary alveolar:	n/a
32	chr7:150748284-150748334	HAEpiC	amniotic membrane:	n/a
33	chr7:150748518-150748568	IMR90	lung:	fetal
34	chr7:150748518-150748568	GM19239	blood:	n/a
35	chr7:150748284-150748334	GM06990	blood:	n/a
36	chr7:150748069-150748119	AG04450	lung:	fetal
37	chr7:150748284-150748334	IMR90	lung:	fetal
38	chr7:150748069-150748119	ECC-1	luminal epithelium:	n/a
39	chr7:150748284-150748334	AG04450	lung:	fetal
40	chr7:150749758-150749808	NH-A	brain:	n/a
41	chr7:150748518-150748568	GM12891	blood:	n/a
42	chr7:150748284-150748334	ProgFib	skin:	n/a
43	chr7:150748069-150748119	PrEC	prostate:	n/a
44	chr7:150749758-150749808	NHBE	bronchial:	n/a
45	chr7:150748518-150748568	HEK293	kidney:	embryo
46	chr7:150748069-150748119	AG09309	skin:	n/a
47	chr7:150748518-150748568	SAEC	small airway:	n/a
48	chr7:150748518-150748568	HCM	heart:	n/a
49	chr7:150748069-150748119	PANC-1	pancreas:	n/a
50	chr7:150748518-150748568	GM12878	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:150064606..150067565-chr7:150746513..150748694,2	MCF-7	breast:

No data

Variant related genes	Relation type
SLC4A2	TF binding region
ASIC3	TF binding region
SLC4A2	CpG island
ASIC3	CpG island
ENSG00000196456	chromatin interactions
ENSG00000214022	chromatin interactions

Extended variants
information (count: 156 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:156 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549586118	chr7:150747478-150747479	Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs193119056	chr7:150747518-150747519	Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs200595590	chr7:150747541-150747542	Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs200274938	chr7:150747548-150747549	Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs369604091	chr7:150747562-150747563	Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs555164678	chr7:150747570-150747571	Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs575137638	chr7:150747590-150747591	Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs116038852	chr7:150747594-150747595	Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs374362547	chr7:150747595-150747596	Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs201153989	chr7:150747599-150747600	Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs114063044	chr7:150747604-150747605	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs149333074	chr7:150747623-150747624	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs377738600	chr7:150747633-150747634	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs536801721	chr7:150747643-150747644	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs62001897	chr7:150747650-150747651	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs148467100	chr7:150747659-150747660	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs368757639	chr7:150747712-150747713	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs373363411	chr7:150747740-150747741	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs376492437	chr7:150747745-150747746	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs2288645	chr7:150747746-150747747	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs547880253	chr7:150747762-150747763	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs561550514	chr7:150747775-150747776	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs527543284	chr7:150747781-150747782	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs184252418	chr7:150747783-150747784	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs564090081	chr7:150747785-150747786	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs532748577	chr7:150747806-150747807	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs549763020	chr7:150747807-150747808	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs569621626	chr7:150747813-150747814	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs535538081	chr7:150747816-150747817	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs548452200	chr7:150747817-150747818	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs144330560	chr7:150747826-150747827	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs200466021	chr7:150747837-150747838	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs377265988	chr7:150747840-150747841	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs554483671	chr7:150747868-150747869	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs577646273	chr7:150747890-150747891	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs114024820	chr7:150747896-150747897	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs147577517	chr7:150747903-150747904	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs112149514	chr7:150747916-150747917	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs200386051	chr7:150747934-150747935	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs11977275	chr7:150747937-150747938	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs201646704	chr7:150747948-150747949	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs3217353	chr7:150747949-150747950	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs140593742	chr7:150747970-150747971	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs369864194	chr7:150747977-150747978	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs374565191	chr7:150747997-150747998	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs571908824	chr7:150748004-150748005	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs377388928	chr7:150748025-150748026	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs370429790	chr7:150748034-150748035	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs373238463	chr7:150748046-150748047	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs540858696	chr7:150748047-150748048	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	16864856	CNVD
Autism	20808228	CNVD
Breast cancer	21509527	CNVD
Ovarian cancer	21720365	CNVD
Heart disease	21282601	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Liver carcinoma	19366792	CNVD
Long-qt syndrome	17576883	CNVD
Bradycardia syndrome	17576883	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Ovarian cancer	21781307	CNVD
Adrenocortical carcinoma	18281524	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:286 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150734000-150748000	Weak transcription	Primary B cells from peripheral blood	blood
2	chr7:150734600-150747800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr7:150736400-150748000	Weak transcription	Psoas Muscle	Psoas
4	chr7:150736800-150753800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr7:150737800-150748200	Weak transcription	Primary hematopoietic stem cells	blood
6	chr7:150738600-150749600	Weak transcription	K562	blood
7	chr7:150739600-150750000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr7:150740200-150753800	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr7:150741400-150748000	Weak transcription	Left Ventricle	heart
10	chr7:150741400-150749400	Weak transcription	Brain Substantia Nigra	brain
11	chr7:150741600-150751200	Weak transcription	Primary B cells from cord blood	blood
12	chr7:150742600-150748000	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr7:150742600-150754400	Weak transcription	Aorta	Aorta
14	chr7:150742800-150750200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
15	chr7:150743000-150748000	Weak transcription	Primary T helper cells fromperipheralblood	blood
16	chr7:150743200-150747800	Weak transcription	Dnd41	blood
17	chr7:150743200-150748000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
18	chr7:150743200-150748800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chr7:150743400-150748000	Weak transcription	Esophagus	oesophagus
20	chr7:150743400-150748000	Weak transcription	Gastric	stomach
21	chr7:150743800-150747800	Weak transcription	Lung	lung
22	chr7:150743800-150748000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr7:150743800-150748000	Weak transcription	Pancreas	Pancrea
24	chr7:150743800-150748000	Weak transcription	Right Ventricle	heart
25	chr7:150743800-150749200	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr7:150743800-150753800	Weak transcription	Liver	Liver
27	chr7:150744000-150748200	Weak transcription	Brain Hippocampus Middle	brain
28	chr7:150744000-150748800	Weak transcription	Primary T cells from cord blood	blood
29	chr7:150744200-150748800	Weak transcription	Brain Angular Gyrus	brain
30	chr7:150744400-150748200	Weak transcription	Fetal Heart	heart
31	chr7:150744400-150751200	Weak transcription	Brain Cingulate Gyrus	brain
32	chr7:150744400-150754000	Weak transcription	A549	lung
33	chr7:150744600-150748000	Weak transcription	HMEC	breast
34	chr7:150744800-150747800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr7:150744800-150748000	Weak transcription	Brain Anterior Caudate	brain
36	chr7:150744800-150748000	Weak transcription	Ovary	ovary
37	chr7:150744800-150754200	Weak transcription	Right Atrium	heart
38	chr7:150745200-150748000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
39	chr7:150745200-150754000	Weak transcription	HSMMtube	muscle
40	chr7:150745200-150754200	Weak transcription	NHDF-Ad	bronchial
41	chr7:150746000-150754000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr7:150746400-150748000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr7:150746600-150749200	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr7:150747000-150747600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr7:150747000-150747600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr7:150747200-150747600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr7:150747200-150749600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
48	chr7:150747400-150747600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr7:150747600-150747800	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr7:150747600-150747800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell

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