Variant report

Variant	esv1801356
Chromosome Location	chr7:128073366-128084133
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:196)
CpG islands
(count:122)
Chromatin interactive
region (count:23)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:196 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:128077923-128078123	K562	blood:	n/a	n/a
2	ARID3A	chr7:128074554-128075237	HepG2	liver:	n/a	n/a
3	ATF1	chr7:128077928-128078143	K562	blood:	n/a	n/a
4	ATF3	chr7:128074349-128075853	A549	lung:	n/a	n/a
5	ATF3	chr7:128075272-128075745	A549	lung:	n/a	n/a
6	BCL3	chr7:128074325-128075776	A549	lung:	n/a	n/a
7	BCL3	chr7:128074365-128075878	A549	lung:	n/a	n/a
8	CBX3	chr7:128077609-128077994	K562	blood:	n/a	n/a
9	CEBPB	chr7:128075379-128075637	HepG2	liver:	n/a	n/a
10	CEBPB	chr7:128075314-128075702	HepG2	liver:	n/a	n/a
11	CEBPB	chr7:128074453-128074839	MCF-7	breast:	n/a	chr7:128074649-128074660
12	CEBPB	chr7:128074403-128074878	A549	lung:	n/a	chr7:128074649-128074660
13	CEBPB	chr7:128074517-128074733	HepG2	liver:	n/a	chr7:128074649-128074660
14	CEBPB	chr7:128075342-128075826	MCF-7	breast:	n/a	n/a
15	CEBPB	chr7:128074511-128074788	HepG2	liver:	n/a	chr7:128074649-128074660
16	CEBPB	chr7:128080879-128080997	K562	blood:	n/a	n/a
17	CEBPB	chr7:128075310-128075737	A549	lung:	n/a	n/a
18	CEBPB	chr7:128074466-128074836	A549	lung:	n/a	chr7:128074649-128074660
19	CEBPB	chr7:128075262-128075792	A549	lung:	n/a	n/a
20	CEBPB	chr7:128074311-128075895	A549	lung:	n/a	chr7:128074649-128074660
21	CEBPB	chr7:128074410-128074941	MCF-7	breast:	n/a	chr7:128074649-128074660
22	CEBPB	chr7:128074510-128074832	HepG2	liver:	n/a	chr7:128074649-128074660
23	CEBPB	chr7:128077847-128078043	K562	blood:	n/a	n/a
24	CEBPB	chr7:128075212-128075692	MCF-7	breast:	n/a	n/a
25	CREB1	chr7:128075376-128075639	A549	lung:	n/a	n/a
26	CREB1	chr7:128074490-128074796	A549	lung:	n/a	n/a
27	CTCF	chr7:128081920-128082070	Caco-2	colon:	n/a	n/a
28	CTCF	chr7:128082600-128082750	HPF	lung:	n/a	n/a
29	CUX1	chr7:128078216-128078218	K562	blood:	n/a	n/a
30	E2F4	chr7:128078887-128079005	MCF10A-Er-Src	breast:	n/a	n/a
31	ELF1	chr7:128075292-128075697	A549	lung:	n/a	n/a
32	ELF1	chr7:128081842-128082089	K562	blood:	n/a	n/a
33	EP300	chr7:128075339-128075716	MCF-7	breast:	n/a	n/a
34	EP300	chr7:128074239-128075972	A549	lung:	n/a	n/a
35	EP300	chr7:128075295-128075708	HepG2	liver:	n/a	n/a
36	EP300	chr7:128083996-128085196	T-47D	breast:	n/a	n/a
37	EP300	chr7:128075316-128075739	MCF-7	breast:	n/a	n/a
38	EP300	chr7:128075413-128075639	HepG2	liver:	n/a	n/a
39	EP300	chr7:128075305-128075708	HepG2	liver:	n/a	n/a
40	EP300	chr7:128074879-128075700	T-47D	breast:	n/a	n/a
41	EP300	chr7:128074691-128075810	T-47D	breast:	n/a	n/a
42	EP300	chr7:128074489-128074890	HepG2	liver:	n/a	n/a
43	EP300	chr7:128074230-128075949	A549	lung:	n/a	n/a
44	ESR1	chr7:128083843-128084704	T-47D	breast:	n/a	chr7:128084259-128084276 chr7:128083970-128083987 chr7:128083969-128083986
45	ESR1	chr7:128075353-128075698	T-47D	breast:	n/a	n/a
46	ESR1	chr7:128083826-128084592	T-47D	breast:	n/a	chr7:128084259-128084276 chr7:128083970-128083987 chr7:128083969-128083986
47	ESR1	chr7:128084026-128084440	T-47D	breast:	n/a	chr7:128084259-128084276
48	ESR1	chr7:128074841-128075676	T-47D	breast:	n/a	n/a
49	ESR1	chr7:128074867-128075217	T-47D	breast:	n/a	n/a
50	ESR1	chr7:128084087-128084541	T-47D	breast:	n/a	chr7:128084259-128084276

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:128080412-128080462	SK-N-SH	brain:	n/a
2	chr7:128080412-128080462	IMR90	lung:	fetal
3	chr7:128079085-128079135	ProgFib	skin:	n/a
4	chr7:128080412-128080462	AG09309	skin:	n/a
5	chr7:128079085-128079135	MCF10A-Er-Src	breast:	n/a
6	chr7:128079085-128079135	SK-N-SH	brain:	n/a
7	chr7:128079085-128079135	AG10803	skin:	n/a
8	chr7:128080412-128080462	ECC-1	luminal epithelium:	n/a
9	chr7:128080412-128080462	Jurkat	blood:	n/a
10	chr7:128079085-128079135	T-47D	breast:	n/a
11	chr7:128080412-128080462	HEK293	kidney:	embryo
12	chr7:128080412-128080462	NHBE	bronchial:	n/a
13	chr7:128080412-128080462	HEEpiC	esophagus:	n/a
14	chr7:128080412-128080462	A549	lung:	n/a
15	chr7:128080412-128080462	Caco-2	colon:	n/a
16	chr7:128079085-128079135	AG04450	lung:	fetal
17	chr7:128079085-128079135	GM19239	blood:	n/a
18	chr7:128080412-128080462	MCF-7	breast:	n/a
19	chr7:128080412-128080462	AG09319	gingival:	n/a
20	chr7:128080412-128080462	T-47D	breast:	n/a
21	chr7:128079085-128079135	SAEC	small airway:	n/a
22	chr7:128079085-128079135	HRCEpiC	kidney:	n/a
23	chr7:128079085-128079135	Caco-2	colon:	n/a
24	chr7:128080412-128080462	HPAEpiC	pulmonary alveolar:	n/a
25	chr7:128080412-128080462	PFSK-1	brain:	n/a
26	chr7:128079085-128079135	HEK293	kidney:	embryo
27	chr7:128079085-128079135	HPAEpiC	pulmonary alveolar:	n/a
28	chr7:128079085-128079135	HCT-116	colon:	n/a
29	chr7:128079085-128079135	HCPEpiC	choroid plexus:	n/a
30	chr7:128080412-128080462	GM19239	blood:	n/a
31	chr7:128079085-128079135	AoSMC	blood vessel:	n/a
32	chr7:128080412-128080462	Hepatocyte	liver:	n/a
33	chr7:128079085-128079135	Jurkat	blood:	n/a
34	chr7:128080412-128080462	H1-hESC	embryonic stem cell:	embryo
35	chr7:128079085-128079135	A549	lung:	n/a
36	chr7:128079085-128079135	SK-N-MC	brain:	n/a
37	chr7:128079085-128079135	HNPCEpiC	eye:	n/a
38	chr7:128079085-128079135	SKMC	muscle:	n/a
39	chr7:128080412-128080462	HCPEpiC	choroid plexus:	n/a
40	chr7:128080412-128080462	SKMC	muscle:	n/a
41	chr7:128079085-128079135	HAEpiC	amniotic membrane:	n/a
42	chr7:128080412-128080462	HCF	heart:	n/a
43	chr7:128079085-128079135	HMEC	breast:	n/a
44	chr7:128080412-128080462	GM12891	blood:	n/a
45	chr7:128080412-128080462	SK-N-MC	brain:	n/a
46	chr7:128080412-128080462	BE2_C	brain:	n/a
47	chr7:128080412-128080462	GM12892	blood:	n/a
48	chr7:128079085-128079135	ECC-1	luminal epithelium:	n/a
49	chr7:128079085-128079135	BJ	skin:	n/a
50	chr7:128079085-128079135	NHDF-neo	bronchial:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:128066135..128077193-chr7:128094256..128102719,54	MCF-7	breast:
2	chr7:128080630..128083451-chr7:128085283..128088252,3	MCF-7	breast:
3	chr7:128071934..128079559-chr7:128081793..128086197,10	MCF-7	breast:
4	chr7:128048480..128050287-chr7:128075489..128078227,2	MCF-7	breast:
5	chr7:128079058..128081650-chr7:128094503..128096174,2	MCF-7	breast:
6	chr7:128045089..128046759-chr7:128073857..128075497,2	MCF-7	breast:
7	chr7:128077598..128080477-chr7:128092228..128095663,3	K562	blood:
8	chr7:128083686..128086427-chr7:128093165..128095584,3	K562	blood:
9	chr7:128081121..128082834-chr7:128084423..128086408,3	K562	blood:
10	chr7:128078754..128080265-chr7:131302994..131305556,2	MCF-7	breast:
11	chr7:128074510..128075893-chr7:128101137..128102142,3	MCF-7	breast:
12	chr7:128066083..128070069-chr7:128074107..128077404,7	MCF-7	breast:
13	chr7:128075023..128077569-chr7:128095918..128098804,2	K562	blood:
14	chr7:128082541..128090035-chr7:128090151..128101015,22	MCF-7	breast:
15	chr7:128073893..128075485-chr7:128078567..128080438,2	K562	blood:
16	chr7:128070995..128071668-chr7:128083750..128084763,3	MCF-7	breast:
17	chr7:128047282..128051646-chr7:128071407..128074955,4	MCF-7	breast:
18	chr7:128077482..128079015-chr7:128094257..128096548,2	MCF-7	breast:
19	chr7:128073893..128075485-chr7:128078567..128080438,2	K562	blood:
20	chr7:128070900..128073511-chr7:128092438..128094017,2	K562	blood:
21	chr7:128071113..128071837-chr7:128083898..128084672,3	MCF-7	breast:
22	chr7:128079136..128080661-chr7:128088834..128090838,2	K562	blood:
23	chr7:128071934..128079559-chr7:128081793..128086197,10	MCF-7	breast:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IMPDH1-2	chr7:128073476-128073767	NONHSAT123190

No data

Variant related genes	Relation type
ENSG00000228700	TF binding region
RNU7-54P	TF binding region
ENSG00000228700	CpG island
RNU7-54P	CpG island
ENSG00000135245	chromatin interactions
ENSG00000106348	chromatin interactions
ENSG00000273184	chromatin interactions
ENSG00000240758	chromatin interactions
ENSG00000238590	chromatin interactions
ENSG00000228700	chromatin interactions

Extended variants
information (count: 329 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:329 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4728108	chr7:128073366-128073367	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs147212689	chr7:128073375-128073376	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs567610029	chr7:128073405-128073406	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs140630148	chr7:128073406-128073407	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs571547053	chr7:128073416-128073417	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs113551661	chr7:128073453-128073454	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs539474539	chr7:128073470-128073471	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs78518207	chr7:128073497-128073498	Weak transcription Enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
9	rs201407324	chr7:128073499-128073500	Weak transcription Enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
10	rs566189701	chr7:128073523-128073524	Weak transcription Enhancers	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
11	rs151145439	chr7:128073672-128073673	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
12	rs1864232	chr7:128073720-128073721	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs573830013	chr7:128073730-128073731	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
14	rs534179679	chr7:128073747-128073748	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
15	rs369441086	chr7:128073789-128073790	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs139068046	chr7:128073820-128073821	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs577736134	chr7:128073848-128073849	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs17152065	chr7:128073858-128073859	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs10233992	chr7:128074010-128074011	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs1014506	chr7:128074042-128074043	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs370068352	chr7:128074063-128074064	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs558064584	chr7:128074177-128074178	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs146466230	chr7:128074194-128074195	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs577895934	chr7:128074205-128074206	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs114876157	chr7:128074206-128074207	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs531224217	chr7:128074215-128074216	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs10954186	chr7:128074243-128074244	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs140656788	chr7:128074273-128074274	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs145828011	chr7:128074306-128074307	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs189258686	chr7:128074341-128074342	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs566177133	chr7:128074437-128074438	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs193104250	chr7:128074562-128074563	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs536769375	chr7:128074597-128074598	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs141445125	chr7:128074610-128074611	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs184565290	chr7:128074674-128074675	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs143218089	chr7:128074682-128074683	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs113568920	chr7:128074787-128074788	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs12112092	chr7:128074819-128074820	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs189015927	chr7:128074866-128074867	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs77476034	chr7:128074874-128074875	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs148300557	chr7:128074959-128074960	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs113998244	chr7:128074960-128074961	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs570865222	chr7:128075002-128075003	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs117860312	chr7:128075029-128075030	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs560841929	chr7:128075034-128075035	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs373441800	chr7:128075052-128075053	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs543063548	chr7:128075070-128075071	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs181491849	chr7:128075086-128075087	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs532905495	chr7:128075117-128075118	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs185639450	chr7:128075148-128075149	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
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
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
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Retinitis pigmentosa	17160897	CNVD
Colorblindness	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Cancer	20164919	CNVD

Chromatin state (count:151 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:128051400-128086200	Weak transcription	Right Atrium	heart
2	chr7:128070200-128074800	Enhancers	Placenta	Placenta
3	chr7:128071200-128074800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr7:128071800-128074400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr7:128071800-128078600	Weak transcription	Adipose Nuclei	Adipose
6	chr7:128072000-128073600	Enhancers	A549	lung
7	chr7:128072200-128074600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr7:128072200-128075000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr7:128072400-128075400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr7:128072600-128074800	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr7:128072600-128075000	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr7:128072600-128075400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr7:128072600-128076200	Enhancers	HepG2	liver
14	chr7:128072800-128075000	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr7:128072800-128075000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr7:128073000-128073600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr7:128073000-128073800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr7:128073000-128074000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr7:128073000-128075000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr7:128073000-128075000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr7:128073200-128073400	Weak transcription	Esophagus	oesophagus
22	chr7:128073200-128074800	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr7:128073400-128073800	Enhancers	Esophagus	oesophagus
24	chr7:128073400-128074000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr7:128073600-128073800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr7:128073600-128074600	Flanking Active TSS	A549	lung
27	chr7:128073800-128083800	Weak transcription	Esophagus	oesophagus
28	chr7:128074000-128075000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr7:128074200-128074400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr7:128074400-128075600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr7:128074400-128076000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr7:128074600-128075600	Active TSS	A549	lung
33	chr7:128074600-128076400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr7:128074800-128075000	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr7:128074800-128075600	Weak transcription	Placenta	Placenta
36	chr7:128074800-128075800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr7:128074800-128076000	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr7:128075000-128075200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
39	chr7:128075000-128075200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr7:128075000-128075200	Bivalent Enhancer	NHLF	lung
41	chr7:128075000-128075400	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr7:128075000-128075600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr7:128075000-128075600	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr7:128075000-128075600	Enhancers	NHEK	skin
45	chr7:128075000-128075800	Enhancers	H1 Cell Line	embryonic stem cell
46	chr7:128075000-128075800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr7:128075000-128075800	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr7:128075000-128076000	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr7:128075000-128076400	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr7:128075000-128076400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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