Variant report

Variant	nsv889130
Chromosome Location	chr7:123875796-124010036
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	ATF1	chr7:123953326-123953442	K562	blood:	n/a	n/a
2	ATF1	chr7:123950919-123951365	K562	blood:	n/a	n/a
3	ATF1	chr7:123886598-123886729	K562	blood:	n/a	n/a
4	ATF1	chr7:123909888-123910120	K562	blood:	n/a	n/a
5	ATF1	chr7:123903518-123903832	K562	blood:	n/a	n/a
6	ATF2	chr7:123903345-123903808	GM12878	blood:	n/a	n/a
7	ATF2	chr7:123897573-123898594	GM12878	blood:	n/a	n/a
8	ATF3	chr7:123903532-123903773	GM12878	blood:	n/a	n/a
9	ATF3	chr7:123903568-123903806	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr7:123903479-123903869	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr7:124009494-124009604	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr7:123903526-123903804	GM12878	blood:	n/a	n/a
13	BATF	chr7:123897707-123898119	GM12878	blood:	n/a	chr7:123897898-123897908 chr7:123897902-123897912 chr7:123897901-123897912
14	BATF	chr7:123885644-123885946	GM12878	blood:	n/a	chr7:123885771-123885782
15	BATF	chr7:123885688-123885883	GM12878	blood:	n/a	chr7:123885771-123885782
16	BATF	chr7:123903522-123903804	GM12878	blood:	n/a	n/a
17	BCL11A	chr7:123885636-123885907	GM12878	blood:	n/a	n/a
18	BCLAF1	chr7:123897642-123898236	GM12878	blood:	n/a	chr7:123898197-123898206 chr7:123897901-123897910
19	BHLHE40	chr7:123885646-123885828	GM12878	blood:	n/a	n/a
20	BHLHE40	chr7:123903573-123903692	GM12878	blood:	n/a	n/a
21	BRCA1	chr7:123915746-123915818	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr7:123903581-123903839	K562	blood:	n/a	chr7:123903693-123903704
23	CEBPB	chr7:124009369-124009705	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr7:123903490-123903892	IMR90	lung:	n/a	chr7:123903693-123903704
25	CEBPB	chr7:123950862-123951209	IMR90	lung:	n/a	n/a
26	CEBPB	chr7:123879901-123880133	A549	lung:	n/a	chr7:123879983-123879994
27	CEBPB	chr7:123903628-123903761	K562	blood:	n/a	chr7:123903693-123903704
28	CEBPB	chr7:123903512-123903887	Hela-S3	cervix:	n/a	chr7:123903693-123903704
29	CEBPB	chr7:123882670-123882986	IMR90	lung:	n/a	chr7:123882811-123882820 chr7:123882811-123882820 chr7:123882811-123882820 chr7:123882811-123882822 chr7:123882809-123882822 chr7:123882809-123882822 chr7:123882811-123882820 chr7:123882809-123882820
30	CEBPB	chr7:123915569-123915830	HepG2	liver:	n/a	chr7:123915698-123915709 chr7:123915698-123915711
31	CEBPB	chr7:123950885-123951358	HCT-116	colon:	n/a	n/a
32	CEBPB	chr7:123950894-123951209	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr7:123882730-123882837	HepG2	liver:	n/a	chr7:123882811-123882820 chr7:123882811-123882820 chr7:123882811-123882820 chr7:123882811-123882822 chr7:123882809-123882822 chr7:123882809-123882822 chr7:123882811-123882820 chr7:123882809-123882820
34	CEBPB	chr7:123882776-123882944	K562	blood:	n/a	chr7:123882811-123882820 chr7:123882811-123882820 chr7:123882811-123882820 chr7:123882811-123882822 chr7:123882809-123882822 chr7:123882809-123882822 chr7:123882811-123882820 chr7:123882809-123882820
35	CEBPB	chr7:124009431-124009635	MCF-7	breast:	n/a	n/a
36	CEBPB	chr7:123903391-123903997	GM12878	blood:	n/a	chr7:123903693-123903704
37	CEBPB	chr7:123950918-123951174	HepG2	liver:	n/a	n/a
38	CEBPB	chr7:123884916-123885153	IMR90	lung:	n/a	n/a
39	CEBPB	chr7:123903529-123903831	A549	lung:	n/a	chr7:123903693-123903704
40	CEBPB	chr7:123882722-123882910	A549	lung:	n/a	chr7:123882811-123882820 chr7:123882811-123882820 chr7:123882811-123882820 chr7:123882811-123882822 chr7:123882809-123882822 chr7:123882809-123882822 chr7:123882811-123882820 chr7:123882809-123882820
41	CEBPB	chr7:124006073-124006379	HepG2	liver:	n/a	n/a
42	CEBPB	chr7:123903472-123904002	HCT-116	colon:	n/a	chr7:123903693-123903704
43	CEBPB	chr7:123903360-123903944	H1-hESC	embryonic stem cell:	n/a	chr7:123903693-123903704
44	CEBPB	chr7:123879945-123880044	HepG2	liver:	n/a	chr7:123879983-123879994
45	CEBPB	chr7:123977376-123977659	HepG2	liver:	n/a	n/a
46	CEBPB	chr7:123903524-123903881	HepG2	liver:	n/a	chr7:123903693-123903704
47	CEBPB	chr7:123903383-123903885	HCT-116	colon:	n/a	chr7:123903693-123903704
48	CEBPB	chr7:123915528-123915868	H1-hESC	embryonic stem cell:	n/a	chr7:123915698-123915709 chr7:123915698-123915711
49	CEBPB	chr7:123901777-123902073	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr7:124000893-124001093	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:123978181-123978231	HAEpiC	amniotic membrane:	n/a
2	chr7:123992223-123992273	GM12891	blood:	n/a
3	chr7:123978181-123978231	HIPEpiC	eye:	n/a
4	chr7:123916407-123916457	NB4	blood:	n/a
5	chr7:123916407-123916457	HCPEpiC	choroid plexus:	n/a
6	chr7:123916407-123916457	HepG2	liver:	n/a
7	chr7:123992223-123992273	HRE	kidney:	n/a
8	chr7:123978181-123978231	AoSMC	blood vessel:	n/a
9	chr7:123916407-123916457	HL-60	blood:	n/a
10	chr7:123916407-123916457	AG09309	skin:	n/a
11	chr7:123978181-123978231	SK-N-MC	brain:	n/a
12	chr7:123916407-123916457	AoSMC	blood vessel:	n/a
13	chr7:123903317-123903367	NB4	blood:	n/a
14	chr7:123903317-123903367	AG09309	skin:	n/a
15	chr7:123916407-123916457	ECC-1	luminal epithelium:	n/a
16	chr7:123916407-123916457	Hela-S3	cervix:	n/a
17	chr7:123916407-123916457	HIPEpiC	eye:	n/a
18	chr7:123916407-123916457	Hepatocyte	liver:	n/a
19	chr7:123978181-123978231	RPTEC	kidney:	n/a
20	chr7:123916407-123916457	GM12878	blood:	n/a
21	chr7:123903317-123903367	A549	lung:	n/a
22	chr7:123992223-123992273	HRCEpiC	kidney:	n/a
23	chr7:123903317-123903367	MCF10A-Er-Src	breast:	n/a
24	chr7:123903317-123903367	HIPEpiC	eye:	n/a
25	chr7:123992223-123992273	HPAEpiC	pulmonary alveolar:	n/a
26	chr7:123978181-123978231	HMEC	breast:	n/a
27	chr7:123978181-123978231	A549	lung:	n/a
28	chr7:123916407-123916457	BE2_C	brain:	n/a
29	chr7:123903317-123903367	Hepatocyte	liver:	n/a
30	chr7:123903317-123903367	SK-N-MC	brain:	n/a
31	chr7:123992223-123992273	GM19239	blood:	n/a
32	chr7:123916407-123916457	RPTEC	kidney:	n/a
33	chr7:123992223-123992273	NH-A	brain:	n/a
34	chr7:123978181-123978231	HRE	kidney:	n/a
35	chr7:123903317-123903367	HCT-116	colon:	n/a
36	chr7:123992223-123992273	GM12892	blood:	n/a
37	chr7:123978181-123978231	AG04449	skin:	fetal
38	chr7:123978181-123978231	Hepatocyte	liver:	n/a
39	chr7:123978181-123978231	NB4	blood:	n/a
40	chr7:123978181-123978231	HRCEpiC	kidney:	n/a
41	chr7:123978181-123978231	HPAEpiC	pulmonary alveolar:	n/a
42	chr7:123992223-123992273	HRPEpiC	eye:	n/a
43	chr7:123978181-123978231	GM19239	blood:	n/a
44	chr7:123992223-123992273	RPTEC	kidney:	n/a
45	chr7:123978181-123978231	MCF-7	breast:	n/a
46	chr7:123903317-123903367	SK-N-SH_RA	brain:	n/a
47	chr7:123978181-123978231	BJ	skin:	n/a
48	chr7:123916407-123916457	HCM	heart:	n/a
49	chr7:123978181-123978231	ECC-1	luminal epithelium:	n/a
50	chr7:123978181-123978231	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr7:123892945..123894583-chr7:123896590..123898487,2	K562	blood:
2	chr7:123919958..123922914-chr7:123935794..123937294,2	K562	blood:
3	chr7:123996206..123998785-chr8:77412686..77415296,2	MCF-7	breast:
4	chr7:123915423..123917674-chr7:123921407..123924592,3	K562	blood:
5	chr7:123938093..123940517-chr7:124074999..124077404,2	K562	blood:
6	chr7:123915423..123917674-chr7:123921407..123924592,3	K562	blood:
7	chr7:123919958..123922914-chr7:123935794..123937294,2	K562	blood:
8	chr7:123887405..123889302-chr7:123890495..123893294,2	K562	blood:
9	chr7:123887405..123889302-chr7:123890495..123893294,2	K562	blood:
10	chr3:64234460..64234993-chr7:123973379..123973879,2	MCF-7	breast:
11	chr7:123892945..123894583-chr7:123896590..123898487,2	K562	blood:
12	chr7:123973378..123975261-chr7:123975911..123978785,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPAM1-3	chr7:124000163-124000252	ENSG00000242593.1
2	lnc-TMEM229A-2	chr7:123977434-123977554	XLOC_006591
3	lnc-TMEM229A-1	chr7:123927269-123927344	NONHSAT123078
4	lnc-TMEM229A-2	chr7:123977434-123977554	XLOC_006591
5	lnc-TMEM229A-1	chr7:123914775-123915052	NONHSAT123078
6	lnc-TMEM229A-1	chr7:123928853-123928879	NONHSAT123078
7	lnc-TMEM229A-1	chr7:123927269-123927598	XLOC_006590
8	lnc-TMEM229A-2	chr7:123982515-123982615	NR_110180
9	lnc-TMEM229A-2	chr7:123989883-123989914	XLOC_006591
10	lnc-TMEM229A-2	chr7:123982515-123982615	XLOC_006591
11	lnc-TMEM229A-1	chr7:123914775-123915052	NONHSAT123077
12	lnc-TMEM229A-1	chr7:123928853-123928911	NONHSAT123077
13	lnc-SPAM1-3	chr7:123974348-123974485	XLOC_006228
14	lnc-TMEM229A-2	chr7:123989883-123989978	XLOC_006591
15	lnc-TMEM229A-2	chr7:123991905-123992154	XLOC_006591
16	lnc-SPAM1-3	chr7:123993205-123993469	XLOC_006228
17	lnc-TMEM229A-1	chr7:123914733-123915052	XLOC_006590
18	lnc-TMEM229A-2	chr7:123982515-123982615	XLOC_006591
19	lnc-TMEM229A-2	chr7:123989883-123989978	NR_110180
20	lnc-SPAM1-3	chr7:123992870-123992905	ENSG00000242593.1
21	lnc-TMEM229A-2	chr7:123977434-123977554	NR_110180
22	lnc-TMEM229A-2	chr7:123991905-123992150	NR_110180
23	lnc-SPAM1-3	chr7:123992870-123992905	XLOC_006228

Variant related genes	Relation type
ENSG00000242593	TF binding region
ENSG00000243574	TF binding region
ENSG00000241324	TF binding region
ENSG00000242593	CpG island
ENSG00000243574	CpG island
ENSG00000241324	CpG island
ENSG00000242593	chromatin interactions
C6orf168	miRNA target sites

Extended variants
information (count: 2514 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:2514 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532308927	chr7:123884611-123884612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs542999227	chr7:123884649-123884650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs13311094	chr7:123884686-123884687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs546038218	chr7:123884691-123884692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs13311440	chr7:123884696-123884697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs13311095	chr7:123884702-123884703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs117432961	chr7:123884710-123884711	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs186617993	chr7:123884735-123884736	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs547863358	chr7:123884749-123884750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs568088422	chr7:123884752-123884753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs527391988	chr7:123884772-123884773	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs547422428	chr7:123884773-123884774	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs570222601	chr7:123884774-123884775	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs538812252	chr7:123884777-123884778	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs558746512	chr7:123884797-123884798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs569184026	chr7:123884813-123884814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs572138981	chr7:123884815-123884816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs190445034	chr7:123884863-123884864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs377136096	chr7:123884906-123884907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs563178091	chr7:123884907-123884908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs13311260	chr7:123884932-123884933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs182990176	chr7:123884949-123884950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs13311215	chr7:123884959-123884960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs4731160	chr7:123884974-123884975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs13311606	chr7:123884984-123884985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs190271193	chr7:123884987-123884988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs562708108	chr7:123885002-123885003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs140713339	chr7:123885020-123885021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs143310675	chr7:123885047-123885048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs561838469	chr7:123885056-123885057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs13311268	chr7:123885058-123885059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs542906368	chr7:123885064-123885065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs531557365	chr7:123885106-123885107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs28437476	chr7:123885116-123885117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs57746866	chr7:123885126-123885127	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs563809201	chr7:123885221-123885222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs148556708	chr7:123885226-123885227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs187881428	chr7:123885233-123885234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs554654737	chr7:123885250-123885251	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs538151743	chr7:123885260-123885261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs13311467	chr7:123885293-123885294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs548814124	chr7:123885300-123885301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs568678458	chr7:123885338-123885339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs560003283	chr7:123885359-123885360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs534173098	chr7:123885371-123885372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs554238246	chr7:123885419-123885420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs577401500	chr7:123885424-123885425	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs193044805	chr7:123885428-123885429	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs556389736	chr7:123885433-123885434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs576257921	chr7:123885435-123885436	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Epilepsy	21635232	CNVD
Squamous cell cancer	20885788	CNVD
Myelofibrosis	22110671	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:176 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:123884600-123884800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr7:123884600-123887200	Enhancers	HMEC	breast
3	chr7:123884800-123885400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr7:123884800-123887200	Enhancers	NHEK	skin
5	chr7:123885400-123887200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr7:123885600-123886600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr7:123885600-123887200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr7:123885800-123887200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr7:123886000-123886200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr7:123886200-123886600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr7:123886200-123886800	Enhancers	NH-A	brain
12	chr7:123886200-123887000	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr7:123886200-123887000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr7:123886200-123887000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr7:123886200-123887000	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr7:123886200-123887200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr7:123886400-123886600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr7:123886400-123886800	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr7:123886400-123886800	Enhancers	HepG2	liver
20	chr7:123886400-123887000	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr7:123886400-123887000	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr7:123886400-123887000	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr7:123886600-123887000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr7:123886600-123887200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr7:123887000-123887600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr7:123887200-123903600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr7:123887600-123889000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr7:123889000-123890800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr7:123890200-123890600	Enhancers	Fetal Lung	lung
30	chr7:123890200-123891400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr7:123890200-123892200	Enhancers	Fetal Heart	heart
32	chr7:123890600-123891600	Weak transcription	Fetal Lung	lung
33	chr7:123891400-123903200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr7:123891600-123892600	Enhancers	Fetal Lung	lung
35	chr7:123892200-123894400	Weak transcription	Fetal Heart	heart
36	chr7:123892600-123893200	Weak transcription	Fetal Lung	lung
37	chr7:123893200-123896000	Enhancers	Fetal Lung	lung
38	chr7:123894400-123894800	Enhancers	Fetal Stomach	stomach
39	chr7:123894400-123897400	Enhancers	Fetal Heart	heart
40	chr7:123894600-123895600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr7:123894800-123899600	Weak transcription	Fetal Stomach	stomach
42	chr7:123895000-123896400	Enhancers	Fetal Brain Male	brain
43	chr7:123896600-123896800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr7:123896800-123902000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr7:123897400-123897800	Flanking Active TSS	Fetal Heart	heart
46	chr7:123897400-123898200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr7:123897400-123898200	Enhancers	Hela-S3	cervix
48	chr7:123897800-123900600	Enhancers	Fetal Heart	heart
49	chr7:123898000-123898200	Enhancers	H9 Cell Line	embryonic stem cell
50	chr7:123898200-123907200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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