Variant report

Variant	esv2761383
Chromosome Location	chr7:150553757-150560322
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr7:150557914-150558043	SK-N-SH_RA	brain:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
2	CTCF	chr7:150556066-150556144	GM19239	blood:	n/a	n/a
3	CTCF	chr7:150556024-150556177	H1-hESC	embryonic stem cell:	n/a	n/a
4	CTCF	chr7:150557840-150557990	NHDF-neo	bronchial:	n/a	chr7:150557965-150557986
5	CTCF	chr7:150557844-150558071	K562	blood:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
6	CTCF	chr7:150557920-150558070	HUVEC	blood vessel:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
7	CTCF	chr7:150557798-150558063	HepG2	liver:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
8	CTCF	chr7:150557980-150558034	MCF-7	breast:	n/a	n/a
9	CTCF	chr7:150558460-150558541	GM19239	blood:	n/a	n/a
10	CTCF	chr7:150557941-150558069	H1-hESC	embryonic stem cell:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
11	CTCF	chr7:150557948-150557984	K562	blood:	n/a	n/a
12	CTCF	chr7:150557900-150558050	SK-N-SH_RA	brain:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
13	CTCF	chr7:150557860-150558010	WERI-Rb-1	eye:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
14	CTCF	chr7:150557900-150558050	Caco-2	colon:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
15	CTCF	chr7:150557938-150558041	Kidney_OC	kidney:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
16	CTCF	chr7:150557876-150558053	HepG2	liver:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
17	CTCF	chr7:150557920-150558070	WERI-Rb-1	eye:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
18	CTCF	chr7:150557790-150558241	K562	blood:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
19	CTCF	chr7:150557924-150558056	K562	blood:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
20	CTCF	chr7:150557860-150558010	HMF	breast:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
21	CTCF	chr7:150557880-150558030	Caco-2	colon:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
22	CTCF	chr7:150555200-150555350	K562	blood:	n/a	n/a
23	CTCF	chr7:150558120-150558270	K562	blood:	n/a	n/a
24	CTCF	chr7:150557900-150558050	RPTEC	kidney:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
25	CTCF	chr7:150557920-150558070	K562	blood:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
26	CTCF	chr7:150557898-150558031	HepG2	liver:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
27	CTCF	chr7:150557945-150558092	Pancreas_OC	pancreas:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
28	CTCF	chr7:150557900-150558050	HepG2	liver:	n/a	chr7:150557973-150557991 chr7:150557965-150557986
29	CTCF	chr7:150557720-150557870	K562	blood:	n/a	n/a
30	HMGN3	chr7:150553614-150553971	K562	blood:	n/a	n/a
31	MAX	chr7:150559321-150559511	H1-hESC	embryonic stem cell:	n/a	n/a
32	MAX	chr7:150558423-150558538	NB4	blood:	n/a	n/a
33	POLR2A	chr7:150558445-150558519	MCF-7	breast:	n/a	n/a
34	RAD21	chr7:150557810-150558076	MCF-7	breast:	n/a	chr7:150557968-150557987
35	RAD21	chr7:150556055-150556131	H1-hESC	embryonic stem cell:	n/a	n/a
36	RAD21	chr7:150557792-150558111	HepG2	liver:	n/a	chr7:150557968-150557987
37	RAD21	chr7:150557862-150558038	K562	blood:	n/a	chr7:150557968-150557987
38	RAD21	chr7:150557794-150558080	H1-hESC	embryonic stem cell:	n/a	chr7:150557968-150557987
39	RAD21	chr7:150557761-150558134	HepG2	liver:	n/a	chr7:150557968-150557987
40	RAD21	chr7:150557247-150558349	SK-N-SH	brain:	n/a	chr7:150557968-150557987 chr7:150557742-150557756 chr7:150557741-150557754
41	RAD21	chr7:150557709-150558154	H1-hESC	embryonic stem cell:	n/a	chr7:150557968-150557987 chr7:150557742-150557756 chr7:150557741-150557754
42	RAD21	chr7:150555922-150556172	H1-hESC	embryonic stem cell:	n/a	n/a
43	RAD21	chr7:150557803-150558059	HepG2	liver:	n/a	chr7:150557968-150557987
44	RAD21	chr7:150557827-150558108	H1-hESC	embryonic stem cell:	n/a	chr7:150557968-150557987
45	RAD21	chr7:150557833-150558118	SK-N-SH_RA	brain:	n/a	chr7:150557968-150557987
46	RAD21	chr7:150555843-150556270	H1-hESC	embryonic stem cell:	n/a	n/a
47	RAD21	chr7:150557709-150558112	SK-N-SH_RA	brain:	n/a	chr7:150557968-150557987 chr7:150557742-150557756 chr7:150557741-150557754
48	SMC3	chr7:150557809-150558115	HepG2	liver:	n/a	n/a
49	UBTF	chr7:150554548-150554660	K562	blood:	n/a	n/a
50	ZNF384	chr7:150558892-150559044	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:150554915-150554965	AG04449	skin:	fetal
2	chr7:150554915-150554965	BJ	skin:	n/a
3	chr7:150554674-150554724	RPTEC	kidney:	n/a
4	chr7:150554915-150554965	NB4	blood:	n/a
5	chr7:150554420-150554470	PrEC	prostate:	n/a
6	chr7:150554628-150554678	SAEC	small airway:	n/a
7	chr7:150554628-150554678	CMK	blood:	n/a
8	chr7:150554674-150554724	HL-60	blood:	n/a
9	chr7:150554113-150554163	HCM	heart:	n/a
10	chr7:150558377-150558427	HRE	kidney:	n/a
11	chr7:150554915-150554965	Caco-2	colon:	n/a
12	chr7:150554420-150554470	HepG2	liver:	n/a
13	chr7:150554674-150554724	AG10803	skin:	n/a
14	chr7:150555302-150555352	HEEpiC	esophagus:	n/a
15	chr7:150554113-150554163	HAEpiC	amniotic membrane:	n/a
16	chr7:150554674-150554724	HCF	heart:	n/a
17	chr7:150554628-150554678	AG09319	gingival:	n/a
18	chr7:150554420-150554470	HRPEpiC	eye:	n/a
19	chr7:150554674-150554724	HAEpiC	amniotic membrane:	n/a
20	chr7:150554113-150554163	HUVEC	blood vessel:	n/a
21	chr7:150554420-150554470	HL-60	blood:	n/a
22	chr7:150558377-150558427	PrEC	prostate:	n/a
23	chr7:150554915-150554965	GM12878	blood:	n/a
24	chr7:150554674-150554724	PFSK-1	brain:	n/a
25	chr7:150558377-150558427	GM19239	blood:	n/a
26	chr7:150554674-150554724	ProgFib	skin:	n/a
27	chr7:150555302-150555352	SK-N-SH	brain:	n/a
28	chr7:150554628-150554678	AG04449	skin:	fetal
29	chr7:150554420-150554470	PANC-1	pancreas:	n/a
30	chr7:150558377-150558427	H1-hESC	embryonic stem cell:	embryo
31	chr7:150558377-150558427	BJ	skin:	n/a
32	chr7:150558377-150558427	AG09319	gingival:	n/a
33	chr7:150558377-150558427	HEK293	kidney:	embryo
34	chr7:150558377-150558427	GM12891	blood:	n/a
35	chr7:150554915-150554965	CMK	blood:	n/a
36	chr7:150554420-150554470	NT2-D1	testis:	n/a
37	chr7:150554420-150554470	K562	blood:	n/a
38	chr7:150554628-150554678	HIPEpiC	eye:	n/a
39	chr7:150554420-150554470	CMK	blood:	n/a
40	chr7:150554113-150554163	HepG2	liver:	n/a
41	chr7:150554628-150554678	NHDF-neo	bronchial:	n/a
42	chr7:150554113-150554163	AG09309	skin:	n/a
43	chr7:150554915-150554965	LNCaP	prostate:	n/a
44	chr7:150554915-150554965	PANC-1	pancreas:	n/a
45	chr7:150558377-150558427	IMR90	lung:	fetal
46	chr7:150554628-150554678	NT2-D1	testis:	n/a
47	chr7:150558377-150558427	GM06990	blood:	n/a
48	chr7:150554420-150554470	ProgFib	skin:	n/a
49	chr7:150554113-150554163	GM12878	blood:	n/a
50	chr7:150554628-150554678	ECC-1	luminal epithelium:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:150550808..150555015-chr7:150558384..150561943,5	K562	blood:
2	chr7:150521643..150523890-chr7:150556049..150558134,2	K562	blood:
3	chr7:150550808..150555015-chr7:150558384..150561943,5	K562	blood:
4	chr7:150550808..150553153-chr7:150558456..150560989,3	K562	blood:
5	chr7:150556165..150558158-chr7:150561303..150563873,2	K562	blood:

Variant related genes	Relation type
AOC1	TF binding region
AOC1	CpG island
ENSG00000002726	chromatin interactions

Extended variants
information (count: 383 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:383 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552872356	chr7:150553762-150553763	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs200206369	chr7:150553831-150553832	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs375216693	chr7:150553833-150553834	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs368493191	chr7:150553838-150553839	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs572549369	chr7:150553842-150553843	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs144106544	chr7:150553850-150553851	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs79934982	chr7:150553851-150553852	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs577618065	chr7:150553856-150553857	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs368923061	chr7:150553858-150553859	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs373164869	chr7:150553888-150553889	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs375159199	chr7:150553894-150553895	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs181034632	chr7:150553934-150553935	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs369516482	chr7:150553960-150553961	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs148613441	chr7:150553974-150553975	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs377655626	chr7:150553977-150553978	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs548803192	chr7:150553995-150553996	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs371090794	chr7:150554035-150554036	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs34502771	chr7:150554037-150554038	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs374455969	chr7:150554048-150554049	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs142034862	chr7:150554112-150554113	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs201603660	chr7:150554114-150554115	Weak transcription Enhancers Strong transcription Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
22	rs374401802	chr7:150554126-150554127	Weak transcription Enhancers Strong transcription Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
23	rs367977707	chr7:150554132-150554133	Weak transcription Enhancers Strong transcription Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
24	rs370771602	chr7:150554147-150554148	Weak transcription Enhancers Strong transcription Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
25	rs374107588	chr7:150554149-150554150	Weak transcription Enhancers Strong transcription Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
26	rs200206446	chr7:150554151-150554152	Weak transcription Enhancers Strong transcription Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
27	rs371999016	chr7:150554157-150554158	Weak transcription Enhancers Strong transcription Bivalent Enhancer	CpG island	1 gene(s)	Overlapped CNVs	n/a
28	rs199733722	chr7:150554171-150554172	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs370764836	chr7:150554172-150554173	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs567581169	chr7:150554215-150554216	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs375856623	chr7:150554218-150554219	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs536155406	chr7:150554233-150554234	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs201353384	chr7:150554255-150554256	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs546811350	chr7:150554257-150554258	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs116444806	chr7:150554261-150554262	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs376957182	chr7:150554285-150554286	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs200653281	chr7:150554299-150554300	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs369508978	chr7:150554309-150554310	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs200778786	chr7:150554310-150554311	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs377701882	chr7:150554314-150554315	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs370158924	chr7:150554356-150554357	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs372468603	chr7:150554368-150554369	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs201727886	chr7:150554394-150554395	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs370340838	chr7:150554396-150554397	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs151141813	chr7:150554401-150554402	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs543446294	chr7:150554421-150554422	Weak transcription Enhancers Strong transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs532287637	chr7:150554433-150554434	Weak transcription Enhancers Strong transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs375861624	chr7:150554434-150554435	Weak transcription Enhancers Strong transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs45568935	chr7:150554452-150554453	Weak transcription Enhancers Strong transcription	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs376059379	chr7:150554459-150554460	Weak transcription Enhancers Strong transcription	CpG island	1 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
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:68 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150539600-150553800	Weak transcription	Liver	Liver
2	chr7:150543200-150557600	Weak transcription	Right Atrium	heart
3	chr7:150549800-150557400	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr7:150549800-150558400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr7:150550000-150557400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr7:150550400-150553800	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr7:150550600-150555000	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr7:150551400-150554400	Weak transcription	Colonic Mucosa	Colon
9	chr7:150551800-150553800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr7:150552200-150553800	Enhancers	HMEC	breast
11	chr7:150552400-150553800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr7:150552800-150553800	Weak transcription	Fetal Intestine Large	intestine
13	chr7:150553200-150558800	Strong transcription	Fetal Intestine Small	intestine
14	chr7:150553400-150554200	Bivalent Enhancer	Placenta	Placenta
15	chr7:150553600-150553800	Flanking Active TSS	Spleen	Spleen
16	chr7:150553600-150554000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr7:150553600-150558800	Strong transcription	Rectal Mucosa Donor 31	rectum
18	chr7:150553600-150559400	Strong transcription	Duodenum Mucosa	Duodenum
19	chr7:150553800-150555200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr7:150553800-150555400	Strong transcription	Liver	Liver
21	chr7:150553800-150556400	Strong transcription	Sigmoid Colon	Sigmoid Colon
22	chr7:150553800-150557400	Weak transcription	Spleen	Spleen
23	chr7:150553800-150558600	Strong transcription	Fetal Intestine Large	intestine
24	chr7:150554000-150556200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr7:150554400-150554800	Strong transcription	Colonic Mucosa	Colon
26	chr7:150554800-150555800	Weak transcription	Colonic Mucosa	Colon
27	chr7:150555000-150561400	Strong transcription	Rectal Mucosa Donor 29	rectum
28	chr7:150555200-150556200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr7:150555400-150556000	Bivalent Enhancer	Placenta	Placenta
30	chr7:150555400-150564000	Weak transcription	Liver	Liver
31	chr7:150555800-150556200	Strong transcription	Colonic Mucosa	Colon
32	chr7:150556200-150557400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr7:150556200-150557600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr7:150556200-150557600	Weak transcription	Colonic Mucosa	Colon
35	chr7:150556400-150557800	Weak transcription	Sigmoid Colon	Sigmoid Colon
36	chr7:150557400-150557800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr7:150557400-150557800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr7:150557400-150558200	ZNF genes & repeats	Spleen	Spleen
39	chr7:150557400-150558400	Enhancers	H1 Cell Line	embryonic stem cell
40	chr7:150557400-150559800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr7:150557600-150557800	Bivalent Enhancer	Placenta	Placenta
42	chr7:150557600-150557800	Strong transcription	Right Atrium	heart
43	chr7:150557600-150558200	Strong transcription	Colonic Mucosa	Colon
44	chr7:150557600-150558200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
45	chr7:150557600-150558400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr7:150557800-150558600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr7:150557800-150559600	Strong transcription	Sigmoid Colon	Sigmoid Colon
48	chr7:150557800-150563000	Weak transcription	Right Atrium	heart
49	chr7:150558200-150558400	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr7:150558200-150562800	Weak transcription	Colonic Mucosa	Colon

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