Variant report

Variant	esv3411371
Chromosome Location	chr7:97735041-97737589
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	ARID3A	chr7:97735655-97736271	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:97735778-97736205	K562	blood:	n/a	n/a
3	ARID3A	chr7:97737548-97738113	HepG2	liver:	n/a	n/a
4	ATF1	chr7:97735552-97736368	K562	blood:	n/a	n/a
5	ATF2	chr7:97735798-97736331	GM12878	blood:	n/a	n/a
6	ATF2	chr7:97735853-97736328	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr7:97735863-97736282	GM12878	blood:	n/a	n/a
8	ATF3	chr7:97735965-97736320	K562	blood:	n/a	chr7:97736168-97736179 chr7:97736174-97736183 chr7:97736148-97736168 chr7:97736179-97736193
9	ATF3	chr7:97735997-97736461	A549	lung:	n/a	chr7:97736168-97736179 chr7:97736174-97736183 chr7:97736148-97736168 chr7:97736179-97736193
10	ATF3	chr7:97735969-97736249	H1-hESC	embryonic stem cell:	n/a	chr7:97736168-97736179 chr7:97736174-97736183 chr7:97736148-97736168 chr7:97736179-97736193
11	ATF3	chr7:97735906-97736370	GM12878	blood:	n/a	chr7:97736168-97736179 chr7:97736174-97736183 chr7:97736148-97736168 chr7:97736179-97736193
12	ATF3	chr7:97735940-97736387	H1-hESC	embryonic stem cell:	n/a	chr7:97736168-97736179 chr7:97736174-97736183 chr7:97736148-97736168 chr7:97736179-97736193
13	ATF3	chr7:97735985-97736348	HepG2	liver:	n/a	chr7:97736168-97736179 chr7:97736174-97736183 chr7:97736148-97736168 chr7:97736179-97736193
14	ATF3	chr7:97736082-97736271	GM12878	blood:	n/a	chr7:97736168-97736179 chr7:97736174-97736183 chr7:97736148-97736168 chr7:97736179-97736193
15	BACH1	chr7:97736066-97736210	K562	blood:	n/a	n/a
16	BACH1	chr7:97736051-97736226	H1-hESC	embryonic stem cell:	n/a	n/a
17	BHLHE40	chr7:97735900-97736375	K562	blood:	n/a	chr7:97736049-97736065
18	BHLHE40	chr7:97735606-97736456	HepG2	liver:	n/a	chr7:97736049-97736065
19	BHLHE40	chr7:97736781-97737091	K562	blood:	n/a	n/a
20	BRCA1	chr7:97736021-97736268	HepG2	liver:	n/a	n/a
21	BRCA1	chr7:97735889-97736315	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr7:97735982-97736272	H1-hESC	embryonic stem cell:	n/a	n/a
23	CBX3	chr7:97735814-97736411	K562	blood:	n/a	n/a
24	CCNT2	chr7:97735963-97736982	K562	blood:	n/a	chr7:97736789-97736798 chr7:97736640-97736649
25	CEBPB	chr7:97735963-97736370	Hela-S3	cervix:	n/a	chr7:97736186-97736194
26	CEBPB	chr7:97735936-97736191	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr7:97736148-97736202	K562	blood:	n/a	chr7:97736186-97736194
28	CEBPB	chr7:97736035-97736195	HepG2	liver:	n/a	chr7:97736186-97736194
29	CEBPD	chr7:97736117-97736390	HepG2	liver:	n/a	n/a
30	CEBPD	chr7:97735956-97736535	K562	blood:	n/a	n/a
31	CHD1	chr7:97736216-97736525	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD1	chr7:97736447-97736515	GM12878	blood:	n/a	n/a
33	CHD2	chr7:97735897-97736349	GM12878	blood:	n/a	n/a
34	CHD2	chr7:97735942-97736362	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr7:97735920-97736610	Hela-S3	cervix:	n/a	n/a
36	CHD2	chr7:97735860-97736739	K562	blood:	n/a	n/a
37	CHD2	chr7:97736014-97736329	HepG2	liver:	n/a	n/a
38	CREB1	chr7:97735572-97736625	HepG2	liver:	n/a	n/a
39	CREB1	chr7:97735825-97736631	H1-hESC	embryonic stem cell:	n/a	n/a
40	CREB1	chr7:97735842-97736620	H1-hESC	embryonic stem cell:	n/a	n/a
41	CREB1	chr7:97735864-97736543	ECC-1	luminal epithelium:	n/a	n/a
42	CREB1	chr7:97735770-97736899	HepG2	liver:	n/a	n/a
43	CREB1	chr7:97735792-97736638	K562	blood:	n/a	n/a
44	CREB1	chr7:97735899-97736562	A549	lung:	n/a	n/a
45	CREB1	chr7:97735946-97736314	A549	lung:	n/a	n/a
46	CREB1	chr7:97735861-97736885	GM12878	blood:	n/a	n/a
47	CREB1	chr7:97735892-97736499	ECC-1	luminal epithelium:	n/a	n/a
48	CREB1	chr7:97735734-97736801	K562	blood:	n/a	n/a
49	CREB1	chr7:97735799-97736629	GM12878	blood:	n/a	n/a
50	CTCF	chr7:97735380-97735530	HAc	cerebellar:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:97735575-97735625	HRE	kidney:	n/a
2	chr7:97735575-97735625	NH-A	brain:	n/a
3	chr7:97736378-97736428	A549	lung:	n/a
4	chr7:97736853-97736903	NB4	blood:	n/a
5	chr7:97736036-97736086	NB4	blood:	n/a
6	chr7:97735575-97735625	HEK293	kidney:	embryo
7	chr7:97735575-97735625	ovcar-3	ovarian:	n/a
8	chr7:97736046-97736096	LNCaP	prostate:	n/a
9	chr7:97736853-97736903	HCT-116	colon:	n/a
10	chr7:97735499-97735549	HepG2	liver:	n/a
11	chr7:97736036-97736086	HMEC	breast:	n/a
12	chr7:97735625-97735675	H1-hESC	embryonic stem cell:	embryo
13	chr7:97735499-97735549	AG04450	lung:	fetal
14	chr7:97736036-97736086	ProgFib	skin:	n/a
15	chr7:97736036-97736086	AG04450	lung:	fetal
16	chr7:97736378-97736428	HPAEpiC	pulmonary alveolar:	n/a
17	chr7:97735499-97735549	A549	lung:	n/a
18	chr7:97735575-97735625	HCF	heart:	n/a
19	chr7:97736378-97736428	GM12891	blood:	n/a
20	chr7:97736360-97736410	HRPEpiC	eye:	n/a
21	chr7:97736138-97736188	RPTEC	kidney:	n/a
22	chr7:97736046-97736096	HIPEpiC	eye:	n/a
23	chr7:97735625-97735675	SK-N-MC	brain:	n/a
24	chr7:97736360-97736410	CMK	blood:	n/a
25	chr7:97736360-97736410	HEEpiC	esophagus:	n/a
26	chr7:97735625-97735675	HRPEpiC	eye:	n/a
27	chr7:97736036-97736086	GM19239	blood:	n/a
28	chr7:97736036-97736086	HUVEC	blood vessel:	n/a
29	chr7:97736046-97736096	HCF	heart:	n/a
30	chr7:97737017-97737067	Hela-S3	cervix:	n/a
31	chr7:97736360-97736410	H1-hESC	embryonic stem cell:	embryo
32	chr7:97736036-97736086	LNCaP	prostate:	n/a
33	chr7:97736126-97736176	MCF10A-Er-Src	breast:	n/a
34	chr7:97737017-97737067	HL-60	blood:	n/a
35	chr7:97737017-97737067	AG09319	gingival:	n/a
36	chr7:97736138-97736188	NHDF-neo	bronchial:	n/a
37	chr7:97735499-97735549	SK-N-SH	brain:	n/a
38	chr7:97736036-97736086	SK-N-SH_RA	brain:	n/a
39	chr7:97735575-97735625	LNCaP	prostate:	n/a
40	chr7:97736126-97736176	GM12892	blood:	n/a
41	chr7:97736126-97736176	HEK293	kidney:	embryo
42	chr7:97736126-97736176	T-47D	breast:	n/a
43	chr7:97735625-97735675	PrEC	prostate:	n/a
44	chr7:97736126-97736176	AG09309	skin:	n/a
45	chr7:97736853-97736903	GM19239	blood:	n/a
46	chr7:97736036-97736086	HIPEpiC	eye:	n/a
47	chr7:97736853-97736903	HepG2	liver:	n/a
48	chr7:97736853-97736903	GM06990	blood:	n/a
49	chr7:97735499-97735549	Caco-2	colon:	n/a
50	chr7:97735499-97735549	SAEC	small airway:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:97736360..97738487-chr7:97758409..97762337,3	K562	blood:
2	chr7:97737313..97739536-chr7:97747241..97749393,2	K562	blood:
3	chr19:13049394..13049962-chr7:97735896..97736709,2	Hela-S3	cervix:
4	chr20:48807269..48810011-chr7:97735604..97737144,2	MCF-7	breast:
5	chr7:97721025..97723015-chr7:97736294..97738071,2	MCF-7	breast:
6	chr7:97735652..97737286-chr7:97753750..97756683,2	MCF-7	breast:
7	chr7:97727895..97730763-chr7:97733389..97735496,2	K562	blood:

Variant related genes	Relation type
LMTK2	TF binding region
LMTK2	CpG island
ENSG00000179218	chromatin interactions
ENSG00000164715	chromatin interactions
ENSG00000172216	chromatin interactions

Extended variants
information (count: 86 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:86 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs77478413	chr7:97735060-97735061	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs559392058	chr7:97735061-97735062	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs55765204	chr7:97735124-97735125	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs553039491	chr7:97735157-97735158	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs571353682	chr7:97735179-97735180	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs548333775	chr7:97735184-97735185	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs182550345	chr7:97735219-97735220	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs77682369	chr7:97735307-97735308	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs552633299	chr7:97735310-97735311	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs557776971	chr7:97735378-97735379	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs571209302	chr7:97735439-97735440	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs187202810	chr7:97735446-97735447	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs111861918	chr7:97735485-97735486	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs371574003	chr7:97735497-97735498	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs112067990	chr7:97735576-97735577	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs536362504	chr7:97735626-97735627	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs118064085	chr7:97735639-97735640	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs576205914	chr7:97735696-97735697	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs537344830	chr7:97735773-97735774	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs551876619	chr7:97735791-97735792	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs149332017	chr7:97735843-97735844	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs573456391	chr7:97735885-97735886	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs374230876	chr7:97735886-97735887	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs540991777	chr7:97735893-97735894	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs398067100	chr7:97735898-97735899	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs397938307	chr7:97735899-97735900	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs552959445	chr7:97735916-97735917	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs574542025	chr7:97735926-97735927	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs541963624	chr7:97736042-97736043	Active TSS Enhancers Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs563895899	chr7:97736064-97736065	Active TSS Enhancers Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs541170036	chr7:97736074-97736075	Active TSS Enhancers Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs150657360	chr7:97736092-97736093	Active TSS Enhancers Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs375979894	chr7:97736114-97736115	Active TSS Enhancers Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs531044836	chr7:97736145-97736146	Active TSS Enhancers Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs546457062	chr7:97736209-97736210	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs564598238	chr7:97736223-97736224	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs555943872	chr7:97736261-97736262	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs528812508	chr7:97736282-97736283	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs547378746	chr7:97736326-97736327	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs201986318	chr7:97736327-97736328	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs565683378	chr7:97736413-97736414	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs36046452	chr7:97736417-97736418	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs529811468	chr7:97736511-97736512	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs146333850	chr7:97736518-97736519	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs548021046	chr7:97736521-97736522	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs77105291	chr7:97736542-97736543	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs3735252	chr7:97736577-97736578	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs78007793	chr7:97736619-97736620	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs75931867	chr7:97736620-97736621	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs536816121	chr7:97736661-97736662	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
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
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	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
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
Metanephric adenoma	20802469	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myoclonus-dystonia	17898012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164920	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Chronic myeloid leukemia	21384125	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bladder cancer	21909424	CNVD
Acute lymphoblastic leukemia	21339820	CNVD

Chromatin state (count:353 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:97733600-97736000	Weak transcription	Right Atrium	heart
2	chr7:97734000-97736000	Enhancers	Fetal Intestine Small	intestine
3	chr7:97734600-97736000	Flanking Active TSS	HepG2	liver
4	chr7:97735200-97735400	Enhancers	Duodenum Mucosa	Duodenum
5	chr7:97735200-97735400	Enhancers	Rectal Mucosa Donor 29	rectum
6	chr7:97735200-97735400	Enhancers	Skeletal Muscle Female	skeletal muscle
7	chr7:97735200-97735400	Enhancers	Hela-S3	cervix
8	chr7:97735200-97735600	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr7:97735200-97735600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr7:97735200-97735800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr7:97735200-97736000	Enhancers	Primary T cells from cord blood	blood
12	chr7:97735200-97736000	Enhancers	Fetal Intestine Large	intestine
13	chr7:97735400-97735600	Enhancers	Brain Angular Gyrus	brain
14	chr7:97735400-97735600	Enhancers	Brain Anterior Caudate	brain
15	chr7:97735400-97735600	Enhancers	Brain Cingulate Gyrus	brain
16	chr7:97735400-97735600	Enhancers	Brain Hippocampus Middle	brain
17	chr7:97735400-97735600	Enhancers	Brain Inferior Temporal Lobe	brain
18	chr7:97735400-97735600	Flanking Active TSS	Esophagus	oesophagus
19	chr7:97735400-97735600	Enhancers	Skeletal Muscle Male	skeletal muscle
20	chr7:97735400-97735600	Enhancers	Dnd41	blood
21	chr7:97735400-97735600	Active TSS	NHEK	skin
22	chr7:97735400-97735800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr7:97735400-97735800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
24	chr7:97735400-97735800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
25	chr7:97735400-97735800	Enhancers	Primary T helper cells PMA-I stimulated	--
26	chr7:97735400-97735800	Enhancers	Right Ventricle	heart
27	chr7:97735400-97735800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
28	chr7:97735400-97735800	Enhancers	HMEC	breast
29	chr7:97735400-97736000	Enhancers	Primary B cells from peripheral blood	blood
30	chr7:97735400-97736000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
31	chr7:97735400-97736000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
32	chr7:97735400-97736000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
33	chr7:97735400-97736000	Flanking Active TSS	Duodenum Mucosa	Duodenum
34	chr7:97735400-97736000	Enhancers	Pancreas	Pancrea
35	chr7:97735400-97736000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
36	chr7:97735400-97736000	Enhancers	Sigmoid Colon	Sigmoid Colon
37	chr7:97735400-97736000	Flanking Active TSS	Hela-S3	cervix
38	chr7:97735400-97736200	Enhancers	Primary T killer memory cells from peripheral blood	blood
39	chr7:97735400-97737400	Active TSS	Stomach Smooth Muscle	stomach
40	chr7:97735600-97735800	Flanking Active TSS	Brain Angular Gyrus	brain
41	chr7:97735600-97735800	Flanking Active TSS	Brain Hippocampus Middle	brain
42	chr7:97735600-97735800	Enhancers	Esophagus	oesophagus
43	chr7:97735600-97735800	Enhancers	Fetal Heart	heart
44	chr7:97735600-97735800	Bivalent Enhancer	Fetal Muscle Leg	muscle
45	chr7:97735600-97735800	Enhancers	Placenta	Placenta
46	chr7:97735600-97735800	Enhancers	Fetal Thymus	thymus
47	chr7:97735600-97735800	Enhancers	K562	blood
48	chr7:97735600-97736000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
49	chr7:97735600-97736000	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
50	chr7:97735600-97736000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin

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