Variant report

Variant	esv1819919
Chromosome Location	chr7:126850298-126888714
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	CEBPB	chr7:126864372-126864434	H1-hESC	embryonic stem cell:	n/a	n/a
2	CHD2	chr7:126876535-126876698	K562	blood:	n/a	n/a
3	CTCF	chr7:126880058-126880097	GM20000	blood:	n/a	n/a
4	CTCF	chr7:126880030-126880112	Fibrobl	skin:	n/a	chr7:126880053-126880071 chr7:126880048-126880069
5	CTCF	chr7:126879974-126880156	LNCaP	prostate:	n/a	chr7:126880053-126880071 chr7:126880048-126880069
6	CTCF	chr7:126880000-126880150	GM12875	blood:	n/a	chr7:126880053-126880071 chr7:126880048-126880069
7	CTCF	chr7:126873516-126873610	Pancreas_OC	pancreas:	n/a	n/a
8	CTCF	chr7:126879940-126880090	MCF-7	breast:	n/a	chr7:126880053-126880071 chr7:126880048-126880069
9	CTCF	chr7:126880000-126880150	Caco-2	colon:	n/a	chr7:126880053-126880071 chr7:126880048-126880069
10	CTCF	chr7:126879960-126880110	GM12878	blood:	n/a	chr7:126880053-126880071 chr7:126880048-126880069
11	CTCF	chr7:126879968-126880170	GM12892	blood:	n/a	chr7:126880053-126880071 chr7:126880048-126880069
12	CTCF	chr7:126880000-126880150	NHLF	lung:	n/a	chr7:126880053-126880071 chr7:126880048-126880069
13	CTCF	chr7:126880020-126880170	HFF-Myc	foreskin:	n/a	chr7:126880053-126880071 chr7:126880048-126880069
14	CTCF	chr7:126880000-126880150	HEK293	kidney:	n/a	chr7:126880053-126880071 chr7:126880048-126880069
15	CTCF	chr7:126879980-126880130	GM12874	blood:	n/a	chr7:126880053-126880071 chr7:126880048-126880069
16	CTCF	chr7:126879940-126880090	NB4	blood:	n/a	chr7:126880053-126880071 chr7:126880048-126880069
17	CTCF	chr7:126879960-126880110	HPAF	blood vessel:	n/a	chr7:126880053-126880071 chr7:126880048-126880069
18	CTCF	chr7:126880100-126880250	A549	lung:	n/a	n/a
19	CTCF	chr7:126879977-126880180	MCF-7	breast:	n/a	chr7:126880053-126880071 chr7:126880048-126880069
20	CTCF	chr7:126879980-126880130	GM12870	blood:	n/a	chr7:126880053-126880071 chr7:126880048-126880069
21	CTCF	chr7:126880027-126880122	ProgFib	skin:	n/a	chr7:126880053-126880071 chr7:126880048-126880069
22	CTCF	chr7:126879912-126880205	K562	blood:	n/a	chr7:126880053-126880071 chr7:126880048-126880069
23	CTCF	chr7:126879880-126880030	HFF-Myc	foreskin:	n/a	n/a
24	CTCF	chr7:126880120-126880270	HRPEpiC	eye:	n/a	n/a
25	CTCF	chr7:126879980-126880130	HRPEpiC	eye:	n/a	chr7:126880053-126880071 chr7:126880048-126880069
26	CTCF	chr7:126879980-126880130	HMF	breast:	n/a	chr7:126880053-126880071 chr7:126880048-126880069
27	CTCF	chr7:126879959-126880174	GM12878	blood:	n/a	chr7:126880053-126880071 chr7:126880048-126880069
28	CTCF	chr7:126879978-126880162	GM19240	blood:	n/a	chr7:126880053-126880071 chr7:126880048-126880069
29	CTCF	chr7:126879966-126880183	GM19238	blood:	n/a	chr7:126880053-126880071 chr7:126880048-126880069
30	CTCF	chr7:126879960-126880110	GM12870	blood:	n/a	chr7:126880053-126880071 chr7:126880048-126880069
31	CTCF	chr7:126880060-126880210	K562	blood:	n/a	n/a
32	CTCF	chr7:126880000-126880150	AG04449	skin:	n/a	chr7:126880053-126880071 chr7:126880048-126880069
33	CTCF	chr7:126880000-126880150	HUVEC	blood vessel:	n/a	chr7:126880053-126880071 chr7:126880048-126880069
34	CTCF	chr7:126866220-126866370	SK-N-SH_RA	brain:	n/a	n/a
35	CTCF	chr7:126879980-126880130	HepG2	liver:	n/a	chr7:126880053-126880071 chr7:126880048-126880069
36	CTCF	chr7:126879973-126880175	A549	lung:	n/a	chr7:126880053-126880071 chr7:126880048-126880069
37	CTCF	chr7:126879999-126880175	Gliobla	brain:	n/a	chr7:126880053-126880071 chr7:126880048-126880069
38	CTCF	chr7:126880000-126880150	GM12865	blood:	n/a	chr7:126880053-126880071 chr7:126880048-126880069
39	CTCF	chr7:126880060-126880210	BE2_C	brain:	n/a	n/a
40	CTCF	chr7:126879980-126880130	GM12867	blood:	n/a	chr7:126880053-126880071 chr7:126880048-126880069
41	CTCF	chr7:126880080-126880230	HL-60	blood:	n/a	n/a
42	CTCF	chr7:126879960-126880110	GM12875	blood:	n/a	chr7:126880053-126880071 chr7:126880048-126880069
43	CTCF	chr7:126879921-126880129	H1-hESC	embryonic stem cell:	n/a	chr7:126880053-126880071 chr7:126880048-126880069
44	CTCF	chr7:126873581-126873622	GM12878	blood:	n/a	n/a
45	CTCF	chr7:126879920-126880210	RPTEC	kidney:	n/a	chr7:126880053-126880071 chr7:126880048-126880069
46	CTCF	chr7:126879943-126880201	K562	blood:	n/a	chr7:126880053-126880071 chr7:126880048-126880069
47	CTCF	chr7:126879979-126880133	HUVEC	blood vessel:	n/a	chr7:126880053-126880071 chr7:126880048-126880069
48	CTCF	chr7:126880000-126880150	GM12866	blood:	n/a	chr7:126880053-126880071 chr7:126880048-126880069
49	CTCF	chr7:126880009-126880149	GM13977	blood:	n/a	chr7:126880053-126880071 chr7:126880048-126880069
50	CTCF	chr7:126879960-126880110	NHEK	skin:	n/a	chr7:126880053-126880071 chr7:126880048-126880069

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:126854672-126854722	HepG2	liver:	n/a
2	chr7:126854672-126854722	HepG2	liver:	n/a
3	chr7:126885001-126885051	HAEpiC	amniotic membrane:	n/a
4	chr7:126884276-126884326	SK-N-SH	brain:	n/a
5	chr7:126882944-126882994	HRPEpiC	eye:	n/a
6	chr7:126883137-126883187	HAEpiC	amniotic membrane:	n/a
7	chr7:126883137-126883187	H1-hESC	embryonic stem cell:	embryo
8	chr7:126854672-126854722	ProgFib	skin:	n/a
9	chr7:126883640-126883690	Caco-2	colon:	n/a
10	chr7:126885001-126885051	HUVEC	blood vessel:	n/a
11	chr7:126854672-126854722	BE2_C	brain:	n/a
12	chr7:126885001-126885051	T-47D	breast:	n/a
13	chr7:126883640-126883690	U87	brain:	n/a
14	chr7:126884276-126884326	ECC-1	luminal epithelium:	n/a
15	chr7:126882944-126882994	HRE	kidney:	n/a
16	chr7:126883137-126883187	HUVEC	blood vessel:	n/a
17	chr7:126882944-126882994	HAEpiC	amniotic membrane:	n/a
18	chr7:126883640-126883690	AoSMC	blood vessel:	n/a
19	chr7:126866923-126866973	AG09309	skin:	n/a
20	chr7:126883137-126883187	NT2-D1	testis:	n/a
21	chr7:126884276-126884326	HCT-116	colon:	n/a
22	chr7:126883640-126883690	GM19239	blood:	n/a
23	chr7:126882944-126882994	GM12891	blood:	n/a
24	chr7:126885001-126885051	NHDF-neo	bronchial:	n/a
25	chr7:126883640-126883690	HCT-116	colon:	n/a
26	chr7:126882944-126882994	LNCaP	prostate:	n/a
27	chr7:126882944-126882994	HNPCEpiC	eye:	n/a
28	chr7:126883640-126883690	SAEC	small airway:	n/a
29	chr7:126883137-126883187	NHBE	bronchial:	n/a
30	chr7:126884276-126884326	HCPEpiC	choroid plexus:	n/a
31	chr7:126884276-126884326	PANC-1	pancreas:	n/a
32	chr7:126884276-126884326	GM12878	blood:	n/a
33	chr7:126885001-126885051	RPTEC	kidney:	n/a
34	chr7:126883137-126883187	AG09309	skin:	n/a
35	chr7:126866923-126866973	HEEpiC	esophagus:	n/a
36	chr7:126884276-126884326	GM12892	blood:	n/a
37	chr7:126883137-126883187	HCF	heart:	n/a
38	chr7:126883137-126883187	GM19239	blood:	n/a
39	chr7:126883137-126883187	Hepatocyte	liver:	n/a
40	chr7:126866923-126866973	T-47D	breast:	n/a
41	chr7:126854672-126854722	SK-N-MC	brain:	n/a
42	chr7:126885001-126885051	HEK293	kidney:	embryo
43	chr7:126883137-126883187	Jurkat	blood:	n/a
44	chr7:126866923-126866973	HRPEpiC	eye:	n/a
45	chr7:126884276-126884326	GM12891	blood:	n/a
46	chr7:126884276-126884326	BJ	skin:	n/a
47	chr7:126883640-126883690	NH-A	brain:	n/a
48	chr7:126854672-126854722	HPAEpiC	pulmonary alveolar:	n/a
49	chr7:126883137-126883187	PrEC	prostate:	n/a
50	chr7:126883137-126883187	ECC-1	luminal epithelium:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:126884896..126891192-chr7:126891657..126895737,6	K562	blood:
2	chr7:126855088..126856692-chr7:126866803..126869023,2	K562	blood:
3	chr7:126841412..126842988-chr7:126847997..126850796,2	K562	blood:
4	chr7:126844024..126846766-chr7:126858329..126861025,2	K562	blood:
5	chr7:126883585..126886396-chr7:126892877..126894797,2	K562	blood:
6	chr7:126879288..126881778-chr7:126885295..126887011,2	K562	blood:
7	chr7:126887307..126889755-chr7:127030651..127034460,3	MCF-7	breast:
8	chr7:126879288..126881778-chr7:126885295..126887011,2	K562	blood:
9	chr7:126859803..126861412-chr7:126868321..126870477,2	K562	blood:
10	chr7:126875739..126881778-chr7:126881781..126887011,8	K562	blood:
11	chr7:126859803..126861412-chr7:126868321..126870477,2	K562	blood:
12	chr7:126884819..126886507-chr7:126900468..126902207,2	K562	blood:
13	chr7:126857935..126859467-chr7:126862307..126865217,2	K562	blood:
14	chr7:126876070..126878246-chr7:126882294..126883841,2	K562	blood:
15	chr7:126857935..126859467-chr7:126862307..126865217,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARF5-3	chr7:126868427-126869975	ENSG00000236340.1
2	lnc-ARF5-3	chr7:126868427-126869087	ENSG00000236340.1
3	lnc-ARF5-3	chr7:126855181-126855307	ENSG00000236340.1
4	lnc-ARF5-3	chr7:126868427-126869975	NR_110195
5	lnc-ARF5-3	chr7:126855181-126855307	ENSG00000236340.1
6	lnc-ARF5-3	chr7:126859521-126859756	ENSG00000236340.1
7	lnc-ARF5-3	chr7:126855181-126855307	NR_110195

Variant related genes	Relation type
ENSG00000236340	TF binding region
GRM8	TF binding region
ENSG00000236340	CpG island
GRM8	CpG island
ENSG00000048405	chromatin interactions
ENSG00000179603	chromatin interactions
ENSG00000236340	chromatin interactions

Extended variants
information (count: 829 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:829 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140624667	chr7:126850318-126850319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs17866784	chr7:126850369-126850370	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs537672910	chr7:126850373-126850374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs188830057	chr7:126850394-126850395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs13233008	chr7:126850445-126850446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs150470155	chr7:126850456-126850457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs13245851	chr7:126850465-126850466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs146608906	chr7:126850467-126850468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs549599062	chr7:126850522-126850523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs2237804	chr7:126850530-126850531	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs6961515	chr7:126850533-126850534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs13233132	chr7:126850573-126850574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs2237805	chr7:126850598-126850599	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs144718653	chr7:126850624-126850625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs576654485	chr7:126850630-126850631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs543690114	chr7:126850735-126850736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs565469880	chr7:126850737-126850738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs533619215	chr7:126850770-126850771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs17866783	chr7:126850806-126850807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs192419176	chr7:126850825-126850826	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs17861419	chr7:126850830-126850831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs184814316	chr7:126850862-126850863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs369587221	chr7:126850863-126850864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs66505540	chr7:126850885-126850886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs67156349	chr7:126850889-126850890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs17864160	chr7:126850895-126850896	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs567481191	chr7:126850898-126850899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs138572371	chr7:126850904-126850905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs549754356	chr7:126850946-126850947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs149254548	chr7:126851017-126851018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs538408345	chr7:126851060-126851061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs17868862	chr7:126851077-126851078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs17869976	chr7:126851107-126851108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs11324768	chr7:126851141-126851142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs34673328	chr7:126851155-126851156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs536628539	chr7:126851176-126851177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs189206326	chr7:126851202-126851203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs112300864	chr7:126851225-126851226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs557058171	chr7:126851253-126851254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs17867313	chr7:126851279-126851280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs554933713	chr7:126851285-126851286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs17866782	chr7:126851291-126851292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs544094254	chr7:126851299-126851300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs565532008	chr7:126851317-126851318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs577528379	chr7:126851384-126851385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs541608547	chr7:126851388-126851389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs573664773	chr7:126851421-126851422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs17863242	chr7:126851448-126851449	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs548741133	chr7:126851462-126851463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs560932969	chr7:126851507-126851508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
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
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
Autism	20808228	CNVD
Prostate cancer	22341455	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:126850000-126852000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr7:126850200-126851000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr7:126852000-126852200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr7:126854800-126855800	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr7:126855000-126856000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr7:126855200-126855600	Enhancers	H9 Cell Line	embryonic stem cell
7	chr7:126855200-126855600	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr7:126855200-126855800	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr7:126855400-126855600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr7:126864200-126864400	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr7:126864200-126864400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr7:126864200-126864800	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr7:126864400-126866600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr7:126864400-126866800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr7:126865000-126865200	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
16	chr7:126866000-126867200	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr7:126866600-126866800	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr7:126866600-126867000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr7:126866600-126867200	Active TSS	ES-I3 Cell Line	embryonic stem cell
20	chr7:126866600-126867400	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr7:126866800-126867000	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr7:126866800-126867400	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr7:126866800-126867400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
24	chr7:126866800-126867600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr7:126866800-126868000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr7:126867000-126867200	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
27	chr7:126867000-126868400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr7:126867200-126869200	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr7:126867400-126867800	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr7:126867600-126869200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr7:126867800-126868000	Enhancers	Brain Hippocampus Middle	brain
32	chr7:126868400-126868600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr7:126869200-126869400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr7:126869200-126869600	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr7:126869200-126869600	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr7:126869400-126869600	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr7:126870600-126870800	Enhancers	Brain Angular Gyrus	brain
38	chr7:126872400-126872600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr7:126872600-126873000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr7:126873000-126873400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr7:126873400-126874800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr7:126874600-126875000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr7:126880600-126881400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr7:126884600-126884800	Bivalent Enhancer	Fetal Kidney	kidney
45	chr7:126885000-126885200	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
46	chr7:126885200-126885600	Enhancers	Fetal Kidney	kidney
47	chr7:126885400-126885800	Enhancers	Liver	Liver
48	chr7:126885400-126886200	Active TSS	Pancreatic Islets	Pancreatic Islet
49	chr7:126885600-126885800	Active TSS	Rectal Mucosa Donor 29	rectum
50	chr7:126885600-126885800	Enhancers	GM12878-XiMat	blood

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