Variant report

Variant	esv1843078
Chromosome Location	chr7:119909603-119934006
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	ATF2	chr7:119912203-119912591	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr7:119912779-119913276	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCLAF1	chr7:119918301-119918776	GM12878	blood:	n/a	chr7:119918522-119918531
4	BCLAF1	chr7:119913502-119914065	GM12878	blood:	n/a	chr7:119913875-119913884 chr7:119913876-119913889 chr7:119913874-119913887
5	BCLAF1	chr7:119912172-119912660	GM12878	blood:	n/a	n/a
6	BHLHE40	chr7:119912233-119913350	GM12878	blood:	n/a	chr7:119913040-119913061
7	BHLHE40	chr7:119912367-119912571	K562	blood:	n/a	n/a
8	BHLHE40	chr7:119913618-119914060	GM12878	blood:	n/a	chr7:119913861-119913877 chr7:119913873-119913889 chr7:119913871-119913887
9	CEBPB	chr7:119913691-119913858	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr7:119910847-119911085	HepG2	liver:	n/a	chr7:119910975-119910986 chr7:119910929-119910940
11	CHD1	chr7:119913734-119913738	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD1	chr7:119913583-119914018	GM12878	blood:	n/a	n/a
13	CHD1	chr7:119912396-119913017	GM12878	blood:	n/a	n/a
14	CHD1	chr7:119912462-119912946	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD2	chr7:119912251-119912498	GM12878	blood:	n/a	n/a
16	CHD2	chr7:119913516-119914058	H1-hESC	embryonic stem cell:	n/a	chr7:119913567-119913577
17	CHD2	chr7:119912991-119913183	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr7:119913032-119914009	GM12878	blood:	n/a	chr7:119913567-119913577
19	CHD2	chr7:119912286-119912637	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTBP2	chr7:119912499-119913239	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTBP2	chr7:119913543-119914327	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr7:119912623-119912630	Gliobla	brain:	n/a	n/a
23	CTCF	chr7:119912280-119912430	GM12870	blood:	n/a	chr7:119912406-119912427 chr7:119912412-119912428 chr7:119912416-119912424 chr7:119912411-119912429
24	CTCF	chr7:119912329-119912559	GM12892	blood:	n/a	chr7:119912406-119912427 chr7:119912412-119912428 chr7:119912416-119912424 chr7:119912411-119912429
25	CTCF	chr7:119912380-119912530	RPTEC	kidney:	n/a	chr7:119912406-119912427 chr7:119912412-119912428 chr7:119912416-119912424 chr7:119912411-119912429
26	CTCF	chr7:119912320-119912470	AG04450	lung:	n/a	chr7:119912406-119912427 chr7:119912412-119912428 chr7:119912416-119912424 chr7:119912411-119912429
27	CTCF	chr7:119913240-119913390	HBMEC	blood vessel:	n/a	n/a
28	CTCF	chr7:119912357-119912518	MCF-7	breast:	n/a	chr7:119912406-119912427 chr7:119912412-119912428 chr7:119912416-119912424 chr7:119912411-119912429
29	CTCF	chr7:119912317-119912563	GM19238	blood:	n/a	chr7:119912406-119912427 chr7:119912412-119912428 chr7:119912416-119912424 chr7:119912411-119912429
30	CTCF	chr7:119912300-119912450	HRPEpiC	eye:	n/a	chr7:119912406-119912427 chr7:119912412-119912428 chr7:119912416-119912424 chr7:119912411-119912429
31	CTCF	chr7:119912600-119912750	GM12872	blood:	n/a	n/a
32	CTCF	chr7:119913220-119913370	GM12873	blood:	n/a	n/a
33	CTCF	chr7:119912380-119912530	HAc	cerebellar:	n/a	chr7:119912406-119912427 chr7:119912412-119912428 chr7:119912416-119912424 chr7:119912411-119912429
34	CTCF	chr7:119912320-119912470	GM12873	blood:	n/a	chr7:119912406-119912427 chr7:119912412-119912428 chr7:119912416-119912424 chr7:119912411-119912429
35	CTCF	chr7:119914370-119914455	GM19240	blood:	n/a	chr7:119914413-119914421
36	CTCF	chr7:119912340-119912490	HEK293	kidney:	n/a	chr7:119912406-119912427 chr7:119912412-119912428 chr7:119912416-119912424 chr7:119912411-119912429
37	CTCF	chr7:119912200-119912672	IMR90	lung:	n/a	chr7:119912406-119912427 chr7:119912412-119912428 chr7:119912416-119912424 chr7:119912411-119912429
38	CTCF	chr7:119912940-119913090	GM12864	blood:	n/a	n/a
39	CTCF	chr7:119913953-119914084	GM19238	blood:	n/a	n/a
40	CTCF	chr7:119912297-119912544	GM19239	blood:	n/a	chr7:119912406-119912427 chr7:119912412-119912428 chr7:119912416-119912424 chr7:119912411-119912429
41	CTCF	chr7:119912177-119912687	K562	blood:	n/a	chr7:119912406-119912427 chr7:119912412-119912428 chr7:119912416-119912424 chr7:119912411-119912429
42	CTCF	chr7:119912340-119912490	AoAF	blood vessel:	n/a	chr7:119912406-119912427 chr7:119912412-119912428 chr7:119912416-119912424 chr7:119912411-119912429
43	CTCF	chr7:119913740-119913890	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr7:119912340-119912490	GM12874	blood:	n/a	chr7:119912406-119912427 chr7:119912412-119912428 chr7:119912416-119912424 chr7:119912411-119912429
45	CTCF	chr7:119912372-119912505	GM12891	blood:	n/a	chr7:119912406-119912427 chr7:119912412-119912428 chr7:119912416-119912424 chr7:119912411-119912429
46	CTCF	chr7:119914360-119914451	GM19238	blood:	n/a	chr7:119914413-119914421
47	CTCF	chr7:119912360-119912510	GM12878	blood:	n/a	chr7:119912406-119912427 chr7:119912412-119912428 chr7:119912416-119912424 chr7:119912411-119912429
48	CTCF	chr7:119912440-119912590	HAc	cerebellar:	n/a	n/a
49	CTCF	chr7:119912320-119912470	GM12872	blood:	n/a	chr7:119912406-119912427 chr7:119912412-119912428 chr7:119912416-119912424 chr7:119912411-119912429
50	CTCF	chr7:119912300-119912450	GM12872	blood:	n/a	chr7:119912406-119912427 chr7:119912412-119912428 chr7:119912416-119912424 chr7:119912411-119912429

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:119912693-119912743	HMEC	breast:	n/a
2	chr7:119912693-119912743	HMEC	breast:	n/a
3	chr7:119914282-119914332	GM19239	blood:	n/a
4	chr7:119915979-119916029	K562	blood:	n/a
5	chr7:119914778-119914828	SKMC	muscle:	n/a
6	chr7:119913683-119913733	H1-hESC	embryonic stem cell:	embryo
7	chr7:119912874-119912924	SK-N-SH	brain:	n/a
8	chr7:119914778-119914828	SK-N-MC	brain:	n/a
9	chr7:119914778-119914828	AG09309	skin:	n/a
10	chr7:119913683-119913733	MCF-7	breast:	n/a
11	chr7:119915258-119915308	AG09309	skin:	n/a
12	chr7:119913771-119913821	HCF	heart:	n/a
13	chr7:119915979-119916029	AG09319	gingival:	n/a
14	chr7:119914578-119914628	AG09319	gingival:	n/a
15	chr7:119914778-119914828	AG04450	lung:	fetal
16	chr7:119912636-119912686	T-47D	breast:	n/a
17	chr7:119914778-119914828	SK-N-SH_RA	brain:	n/a
18	chr7:119915076-119915126	NHBE	bronchial:	n/a
19	chr7:119912636-119912686	ovcar-3	ovarian:	n/a
20	chr7:119915979-119916029	HMEC	breast:	n/a
21	chr7:119912900-119912950	AG04449	skin:	fetal
22	chr7:119912636-119912686	GM19239	blood:	n/a
23	chr7:119914578-119914628	NHDF-neo	bronchial:	n/a
24	chr7:119915979-119916029	H1-hESC	embryonic stem cell:	embryo
25	chr7:119914778-119914828	HRPEpiC	eye:	n/a
26	chr7:119913771-119913821	HepG2	liver:	n/a
27	chr7:119912636-119912686	PFSK-1	brain:	n/a
28	chr7:119913368-119913418	HCM	heart:	n/a
29	chr7:119912900-119912950	HCPEpiC	choroid plexus:	n/a
30	chr7:119912636-119912686	MCF10A-Er-Src	breast:	n/a
31	chr7:119913771-119913821	Hepatocyte	liver:	n/a
32	chr7:119913771-119913821	HCPEpiC	choroid plexus:	n/a
33	chr7:119912636-119912686	HRCEpiC	kidney:	n/a
34	chr7:119912874-119912924	PFSK-1	brain:	n/a
35	chr7:119915979-119916029	Caco-2	colon:	n/a
36	chr7:119913771-119913821	BE2_C	brain:	n/a
37	chr7:119912723-119912773	PFSK-1	brain:	n/a
38	chr7:119914778-119914828	HCPEpiC	choroid plexus:	n/a
39	chr7:119914282-119914332	GM06990	blood:	n/a
40	chr7:119915979-119916029	BE2_C	brain:	n/a
41	chr7:119912693-119912743	MCF-7	breast:	n/a
42	chr7:119914282-119914332	GM12892	blood:	n/a
43	chr7:119912723-119912773	NHDF-neo	bronchial:	n/a
44	chr7:119915484-119915534	AG04449	skin:	fetal
45	chr7:119914778-119914828	ovcar-3	ovarian:	n/a
46	chr7:119912900-119912950	HEK293	kidney:	embryo
47	chr7:119912874-119912924	SKMC	muscle:	n/a
48	chr7:119912874-119912924	AoSMC	blood vessel:	n/a
49	chr7:119912636-119912686	ECC-1	luminal epithelium:	n/a
50	chr7:119912636-119912686	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:119915799..119917690-chr7:119919772..119921442,2	K562	blood:
2	chr7:119915799..119917690-chr7:119919772..119921442,2	K562	blood:
3	chr7:119881073..119883750-chr7:119914172..119916717,3	K562	blood:
4	chr7:119923379..119926159-chr7:119930108..119932380,2	K562	blood:
5	chr7:119918513..119920126-chr7:119921372..119923072,2	K562	blood:
6	chr7:119575228..119576234-chr7:119911967..119912836,4	MCF-7	breast:
7	chr7:119918513..119920126-chr7:119921372..119923072,2	K562	blood:
8	chr7:119923379..119926159-chr7:119930108..119932380,2	K562	blood:

Variant related genes	Relation type
KCND2	TF binding region
KCND2	CpG island

Extended variants
information (count: 785 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:785 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543275092	chr7:119909615-119909616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs182423174	chr7:119909624-119909625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs574338794	chr7:119909723-119909724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs528858182	chr7:119909785-119909786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs79924201	chr7:119909797-119909798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs79412543	chr7:119909798-119909799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs2402524	chr7:119909872-119909873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs539868389	chr7:119909903-119909904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs76282920	chr7:119909923-119909924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs372023051	chr7:119909981-119909982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs559383549	chr7:119910000-119910001	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs528204119	chr7:119910015-119910016	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs59666338	chr7:119910037-119910038	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs186857060	chr7:119910042-119910043	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs532273799	chr7:119910073-119910074	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs375629029	chr7:119910091-119910092	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs368471944	chr7:119910100-119910101	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs531978551	chr7:119910101-119910102	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs199770139	chr7:119910159-119910160	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs548589851	chr7:119910160-119910161	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs10279729	chr7:119910207-119910208	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs192858568	chr7:119910225-119910226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs112247000	chr7:119910249-119910250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs184783671	chr7:119910270-119910271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs539942987	chr7:119910287-119910288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs10224017	chr7:119910318-119910319	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs188511469	chr7:119910374-119910375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs568950592	chr7:119910389-119910390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs554266138	chr7:119910392-119910393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs192989024	chr7:119910435-119910436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs372109194	chr7:119910445-119910446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs184706031	chr7:119910506-119910507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs574696587	chr7:119910563-119910564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs78519013	chr7:119910567-119910568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs553358394	chr7:119910577-119910578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs576479681	chr7:119910696-119910697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs545490501	chr7:119910723-119910724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs547319793	chr7:119910737-119910738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs536635436	chr7:119910755-119910756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs562643199	chr7:119910852-119910853	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs78661048	chr7:119910973-119910974	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs542436940	chr7:119910976-119910977	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs555429267	chr7:119910984-119910985	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs562212222	chr7:119910988-119910989	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs574089002	chr7:119911081-119911082	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs528001108	chr7:119911112-119911113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs114947131	chr7:119911125-119911126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs564470302	chr7:119911146-119911147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs73429951	chr7:119911147-119911148	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs553434574	chr7:119911273-119911274	Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Myelofibrosis	22110671	CNVD
Renal cell carcinoma	18194544	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:359 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:119904200-119912000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr7:119908200-119910600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr7:119908200-119911400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr7:119910000-119910200	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr7:119910400-119912000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr7:119910600-119910800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr7:119910800-119911000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr7:119910800-119911200	Enhancers	Brain Anterior Caudate	brain
9	chr7:119911000-119911200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr7:119911200-119912200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr7:119911400-119911600	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr7:119911400-119911600	Bivalent/Poised TSS	Brain Angular Gyrus	brain
13	chr7:119911400-119912000	Enhancers	Fetal Brain Male	brain
14	chr7:119911400-119912200	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr7:119911400-119912200	Enhancers	Fetal Brain Female	brain
16	chr7:119911400-119912400	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr7:119911400-119914800	Active TSS	Brain Anterior Caudate	brain
18	chr7:119911600-119912000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr7:119911600-119912000	Enhancers	GM12878-XiMat	blood
20	chr7:119911600-119914400	Active TSS	Brain Angular Gyrus	brain
21	chr7:119912000-119912400	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr7:119912000-119912400	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr7:119912000-119912400	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr7:119912000-119912400	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
25	chr7:119912000-119914000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
26	chr7:119912000-119914400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
27	chr7:119912000-119914600	Active TSS	Brain Inferior Temporal Lobe	brain
28	chr7:119912000-119914600	Active TSS	Fetal Brain Male	brain
29	chr7:119912000-119914600	Active TSS	GM12878-XiMat	blood
30	chr7:119912000-119914800	Active TSS	Brain Substantia Nigra	brain
31	chr7:119912200-119912400	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr7:119912200-119912400	Enhancers	H1 Cell Line	embryonic stem cell
33	chr7:119912200-119912400	Enhancers	H9 Cell Line	embryonic stem cell
34	chr7:119912200-119912400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr7:119912200-119912400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
36	chr7:119912200-119912400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr7:119912200-119912400	Active TSS	Adipose Nuclei	Adipose
38	chr7:119912200-119912400	Bivalent Enhancer	HMEC	breast
39	chr7:119912200-119912400	Enhancers	Osteobl	bone
40	chr7:119912200-119912600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr7:119912200-119912600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr7:119912200-119912600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr7:119912200-119912800	Active TSS	Brain Germinal Matrix	brain
44	chr7:119912200-119914000	Active TSS	Fetal Brain Female	brain
45	chr7:119912200-119914000	Bivalent/Poised TSS	Fetal Lung	lung
46	chr7:119912200-119914200	Active TSS	Fetal Kidney	kidney
47	chr7:119912200-119914400	Active TSS	Brain Hippocampus Middle	brain
48	chr7:119912200-119914600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr7:119912200-119914600	Active TSS	Ovary	ovary
50	chr7:119912200-119914800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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