Variant report

Variant	nsv889089
Chromosome Location	chr7:117865940-117921267
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	chr7:117899979-117900108	K562	blood:	n/a	n/a
2	ATF1	chr7:117874383-117874398	K562	blood:	n/a	n/a
3	BATF	chr7:117885444-117885730	GM12878	blood:	n/a	chr7:117885558-117885569
4	BATF	chr7:117885454-117885744	GM12878	blood:	n/a	chr7:117885558-117885569
5	BHLHE40	chr7:117885421-117885756	GM12878	blood:	n/a	n/a
6	BHLHE40	chr7:117878791-117879013	GM12878	blood:	n/a	n/a
7	CEBPB	chr7:117917281-117917569	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr7:117878297-117878579	A549	lung:	n/a	n/a
9	CEBPB	chr7:117875591-117875703	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD2	chr7:117879141-117879172	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr7:117891060-117891210	GM12869	blood:	n/a	chr7:117891128-117891146 chr7:117891133-117891141 chr7:117891129-117891145 chr7:117891123-117891144
12	CTCF	chr7:117885120-117885270	SK-N-SH_RA	brain:	n/a	n/a
13	CTCF	chr7:117899300-117899450	RPTEC	kidney:	n/a	chr7:117899340-117899356
14	CTCF	chr7:117891160-117891310	RPTEC	kidney:	n/a	n/a
15	CTCF	chr7:117891053-117891239	LNCaP	prostate:	n/a	chr7:117891128-117891146 chr7:117891133-117891141 chr7:117891129-117891145 chr7:117891123-117891144
16	CTCF	chr7:117891130-117891141	GM13977	blood:	n/a	chr7:117891133-117891141
17	CTCF	chr7:117891100-117891250	HPF	lung:	n/a	chr7:117891128-117891146 chr7:117891133-117891141 chr7:117891129-117891145 chr7:117891123-117891144
18	CTCF	chr7:117891080-117891189	Kidney_OC	kidney:	n/a	chr7:117891128-117891146 chr7:117891133-117891141 chr7:117891129-117891145 chr7:117891123-117891144
19	CTCF	chr7:117891080-117891230	AG09319	gingival:	n/a	chr7:117891128-117891146 chr7:117891133-117891141 chr7:117891129-117891145 chr7:117891123-117891144
20	CTCF	chr7:117899180-117899408	A549	lung:	n/a	chr7:117899340-117899356
21	CTCF	chr7:117899302-117899406	Lung_OC	lung:	n/a	chr7:117899340-117899356
22	CTCF	chr7:117891040-117891190	Hela-S3	cervix:	n/a	chr7:117891128-117891146 chr7:117891133-117891141 chr7:117891129-117891145 chr7:117891123-117891144
23	CTCF	chr7:117891020-117891170	AG09319	gingival:	n/a	chr7:117891128-117891146 chr7:117891133-117891141 chr7:117891129-117891145 chr7:117891123-117891144
24	CTCF	chr7:117891018-117891246	SK-N-SH_RA	brain:	n/a	chr7:117891128-117891146 chr7:117891133-117891141 chr7:117891129-117891145 chr7:117891123-117891144
25	CTCF	chr7:117899275-117899431	Hela-S3	cervix:	n/a	chr7:117899340-117899356
26	CTCF	chr7:117891020-117891170	HEK293	kidney:	n/a	chr7:117891128-117891146 chr7:117891133-117891141 chr7:117891129-117891145 chr7:117891123-117891144
27	CTCF	chr7:117891060-117891210	GM12871	blood:	n/a	chr7:117891128-117891146 chr7:117891133-117891141 chr7:117891129-117891145 chr7:117891123-117891144
28	CTCF	chr7:117899200-117899350	AoAF	blood vessel:	n/a	n/a
29	CTCF	chr7:117891090-117891194	GM12878	blood:	n/a	chr7:117891128-117891146 chr7:117891133-117891141 chr7:117891129-117891145 chr7:117891123-117891144
30	CTCF	chr7:117891040-117891190	HEK293	kidney:	n/a	chr7:117891128-117891146 chr7:117891133-117891141 chr7:117891129-117891145 chr7:117891123-117891144
31	CTCF	chr7:117891048-117891236	HUVEC	blood vessel:	n/a	chr7:117891128-117891146 chr7:117891133-117891141 chr7:117891129-117891145 chr7:117891123-117891144
32	CTCF	chr7:117891100-117891250	AG04450	lung:	n/a	chr7:117891128-117891146 chr7:117891133-117891141 chr7:117891129-117891145 chr7:117891123-117891144
33	CTCF	chr7:117899243-117899429	Medullo	brain:	n/a	chr7:117899340-117899356
34	CTCF	chr7:117891080-117891230	GM12878	blood:	n/a	chr7:117891128-117891146 chr7:117891133-117891141 chr7:117891129-117891145 chr7:117891123-117891144
35	CTCF	chr7:117891080-117891230	GM12867	blood:	n/a	chr7:117891128-117891146 chr7:117891133-117891141 chr7:117891129-117891145 chr7:117891123-117891144
36	CTCF	chr7:117891040-117891190	K562	blood:	n/a	chr7:117891128-117891146 chr7:117891133-117891141 chr7:117891129-117891145 chr7:117891123-117891144
37	CTCF	chr7:117899142-117899607	SK-N-SH	brain:	n/a	chr7:117899340-117899356
38	CTCF	chr7:117891092-117891213	Pancreas_OC	pancreas:	n/a	chr7:117891128-117891146 chr7:117891133-117891141 chr7:117891129-117891145 chr7:117891123-117891144
39	CTCF	chr7:117891060-117891210	HCM	heart:	n/a	chr7:117891128-117891146 chr7:117891133-117891141 chr7:117891129-117891145 chr7:117891123-117891144
40	CTCF	chr7:117891040-117891190	HA-sp	spinal cord:	n/a	chr7:117891128-117891146 chr7:117891133-117891141 chr7:117891129-117891145 chr7:117891123-117891144
41	CTCF	chr7:117891060-117891210	HUVEC	blood vessel:	n/a	chr7:117891128-117891146 chr7:117891133-117891141 chr7:117891129-117891145 chr7:117891123-117891144
42	CTCF	chr7:117891060-117891210	HepG2	liver:	n/a	chr7:117891128-117891146 chr7:117891133-117891141 chr7:117891129-117891145 chr7:117891123-117891144
43	CTCF	chr7:117891040-117891190	HPAF	blood vessel:	n/a	chr7:117891128-117891146 chr7:117891133-117891141 chr7:117891129-117891145 chr7:117891123-117891144
44	CTCF	chr7:117891040-117891190	HEEpiC	esophagus:	n/a	chr7:117891128-117891146 chr7:117891133-117891141 chr7:117891129-117891145 chr7:117891123-117891144
45	CTCF	chr7:117899300-117899450	GM12873	blood:	n/a	chr7:117899340-117899356
46	CTCF	chr7:117891060-117891210	AG10803	skin:	n/a	chr7:117891128-117891146 chr7:117891133-117891141 chr7:117891129-117891145 chr7:117891123-117891144
47	CTCF	chr7:117890960-117891110	HVMF	connective:	n/a	n/a
48	CTCF	chr7:117899172-117899538	GM12878	blood:	n/a	chr7:117899340-117899356
49	CTCF	chr7:117891060-117891210	HCFaa	heart:	n/a	chr7:117891123-117891144 chr7:117891128-117891146 chr7:117891133-117891141 chr7:117891129-117891145
50	CTCF	chr7:117899280-117899430	GM06990	blood:	n/a	chr7:117899340-117899356

No.	Distal block	Cell Line	Cell type
1	chr7:117884617..117887581-chr7:117888612..117890526,2	MCF-7	breast:
2	chr7:117858675..117860839-chr7:117870370..117872666,2	K562	blood:
3	chr7:117884069..117886965-chr7:117888003..117890494,2	K562	blood:
4	chr7:117896836..117898493-chr7:117900097..117902043,2	K562	blood:
5	chr7:117821797..117823895-chr7:117873522..117875796,2	MCF-7	breast:
6	chr7:117914543..117916311-chr7:117931955..117934025,2	K562	blood:
7	chr7:117861485..117863547-chr7:117866235..117868963,2	K562	blood:
8	chr7:117858469..117860839-chr7:117870370..117873011,3	K562	blood:
9	chr7:117822582..117824978-chr7:117867664..117869545,2	MCF-7	breast:
10	chr7:117867427..117869057-chr7:117871203..117872757,2	K562	blood:
11	chr7:117884069..117886965-chr7:117888003..117890494,2	K562	blood:
12	chr7:117867427..117869057-chr7:117871203..117872757,2	K562	blood:
13	chr7:117896836..117898493-chr7:117900097..117902043,2	K562	blood:
14	chr7:117893799..117896241-chr7:117904650..117906874,2	K562	blood:
15	chr7:117916864..117919001-chr7:117920265..117922583,2	MCF-7	breast:
16	chr7:117893799..117896241-chr7:117904650..117906874,2	K562	blood:
17	chr7:117874784..117876753-chr7:117884123..117886135,2	K562	blood:
18	chr7:117898898..117901210-chr7:117904773..117907240,2	K562	blood:
19	chr7:117898898..117901210-chr7:117904773..117907240,2	K562	blood:
20	chr7:117835525..117838380-chr7:117865050..117867504,3	K562	blood:
21	chr7:117845682..117847702-chr7:117872075..117874755,2	K562	blood:
22	chr7:117884617..117887581-chr7:117888612..117890526,2	MCF-7	breast:
23	chr7:117916864..117919001-chr7:117920265..117922583,2	MCF-7	breast:
24	chr7:117874784..117876753-chr7:117884123..117886135,2	K562	blood:
25	chr7:117823258..117824835-chr7:117869393..117871803,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANKRD7-1	chr7:117879882-117880052	NONHSAT122976
2	lnc-ANKRD7-1	chr7:117874755-117874928	NONHSAT122960
3	lnc-ANKRD7-1	chr7:117879963-117880041	NONHSAT122960
4	lnc-ANKRD7-1	chr7:117882403-117882769	NONHSAT122976
5	lnc-ANKRD7-1	chr7:117874485-117874599	NONHSAT122960
6	lnc-ANKRD7-1	chr7:117876095-117876201	NONHSAT122960
7	lnc-ANKRD7-1	chr7:117876844-117876980	NONHSAT122960

Variant related genes	Relation type
ANKRD7	TF binding region
ENSG00000128534	chromatin interactions

Extended variants
information (count: 1432 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1432 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539728592	chr7:117866006-117866007	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs557958158	chr7:117866007-117866008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs372014884	chr7:117866096-117866097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs57002169	chr7:117866098-117866099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs192042240	chr7:117866206-117866207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs34127409	chr7:117866211-117866212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs562173955	chr7:117866252-117866253	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs573956617	chr7:117866262-117866263	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs541390742	chr7:117866336-117866337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs143300799	chr7:117866396-117866397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs367993732	chr7:117866397-117866398	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs149041057	chr7:117866410-117866411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs533291256	chr7:117866412-117866413	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs142107243	chr7:117866472-117866473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs563513907	chr7:117866548-117866549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs571472027	chr7:117866584-117866585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs566730820	chr7:117866585-117866586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs567577997	chr7:117866630-117866631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs183982030	chr7:117866650-117866651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs80314324	chr7:117866653-117866654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs567325787	chr7:117866660-117866661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs188522162	chr7:117866673-117866674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs151180526	chr7:117866678-117866679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs570888332	chr7:117866717-117866718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192128906	chr7:117866731-117866732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs140249076	chr7:117866799-117866800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs558021526	chr7:117866859-117866860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372898146	chr7:117866870-117866871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs145461696	chr7:117866887-117866888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs537606351	chr7:117866922-117866923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs538799239	chr7:117866929-117866930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs555605113	chr7:117866977-117866978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs184340297	chr7:117866986-117866987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs541142128	chr7:117867019-117867020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs116184120	chr7:117867023-117867024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs115900713	chr7:117867025-117867026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs545329415	chr7:117867065-117867066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs187190527	chr7:117867105-117867106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs575382266	chr7:117867130-117867131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs372453840	chr7:117867161-117867162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs57970913	chr7:117867199-117867200	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs560909389	chr7:117867202-117867203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs372847009	chr7:117867261-117867262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs528219380	chr7:117867305-117867306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs369258811	chr7:117867311-117867312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs546375017	chr7:117867319-117867320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs570951695	chr7:117867320-117867321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs191644607	chr7:117867355-117867356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs184412432	chr7:117867382-117867383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs569988263	chr7:117867429-117867430	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Acute myeloid leukemia	21251322	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	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
Schizophrenia	21346763	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:83 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:117866000-117866400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr7:117866000-117866600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr7:117866000-117866600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr7:117866600-117867400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr7:117867400-117867600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr7:117871000-117871400	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr7:117871000-117871800	Enhancers	Dnd41	blood
8	chr7:117871000-117872000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr7:117871600-117871800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr7:117871600-117871800	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr7:117871600-117872000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr7:117871800-117872000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr7:117872000-117872400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr7:117872000-117872400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr7:117872000-117872800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr7:117872000-117873200	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr7:117872400-117873200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr7:117872400-117873200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr7:117872400-117873800	Enhancers	HMEC	breast
20	chr7:117872600-117873000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr7:117872600-117873000	Enhancers	NH-A	brain
22	chr7:117872600-117873600	Enhancers	NHEK	skin
23	chr7:117872600-117873800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr7:117872800-117873400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr7:117872800-117873400	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr7:117872800-117873400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr7:117872800-117873600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr7:117872800-117874000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr7:117873000-117873400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr7:117873200-117873600	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr7:117873400-117878200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr7:117873400-117878400	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr7:117878200-117878600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr7:117878400-117879000	Enhancers	Cortex derived primary cultured neurospheres	brain
35	chr7:117878400-117879400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr7:117878800-117879400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr7:117879000-117879600	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr7:117879400-117879600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr7:117884800-117886400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr7:117885000-117885400	Enhancers	GM12878-XiMat	blood
41	chr7:117885000-117885600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr7:117885000-117885600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr7:117885000-117886200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr7:117885000-117886200	Enhancers	Dnd41	blood
45	chr7:117885200-117885600	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr7:117885200-117885600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr7:117885200-117885600	Enhancers	NH-A	brain
48	chr7:117885200-117885800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr7:117885200-117885800	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr7:117885200-117885800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links