Variant report

Variant	nsv1029901
Chromosome Location	chr7:18205779-18387956
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1506)
CpG islands
(count:305)
Chromatin interactive
region (count:94)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1506 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:18217852-18218274	K562	blood:	n/a	n/a
2	ARID3A	chr7:18303709-18303826	K562	blood:	n/a	n/a
3	ARID3A	chr7:18230594-18230697	K562	blood:	n/a	n/a
4	ARID3A	chr7:18231163-18231437	K562	blood:	n/a	n/a
5	ARID3A	chr7:18218013-18218198	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:18216717-18217627	K562	blood:	n/a	n/a
7	ATF1	chr7:18301886-18302085	K562	blood:	n/a	n/a
8	ATF1	chr7:18216885-18217560	K562	blood:	n/a	n/a
9	ATF1	chr7:18329927-18330098	K562	blood:	n/a	n/a
10	ATF1	chr7:18355303-18355464	K562	blood:	n/a	n/a
11	ATF1	chr7:18360525-18360954	K562	blood:	n/a	n/a
12	ATF1	chr7:18217858-18218308	K562	blood:	n/a	n/a
13	ATF1	chr7:18214616-18214939	K562	blood:	n/a	n/a
14	ATF2	chr7:18217364-18218418	GM12878	blood:	n/a	n/a
15	ATF3	chr7:18217814-18218252	K562	blood:	n/a	n/a
16	BACH1	chr7:18385285-18385657	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr7:18360062-18360314	K562	blood:	n/a	n/a
18	BATF	chr7:18218797-18219127	GM12878	blood:	n/a	n/a
19	BATF	chr7:18217858-18218265	GM12878	blood:	n/a	n/a
20	BATF	chr7:18217382-18217699	GM12878	blood:	n/a	n/a
21	BATF	chr7:18217334-18217781	GM12878	blood:	n/a	n/a
22	BCL11A	chr7:18217377-18217760	GM12878	blood:	n/a	n/a
23	BCLAF1	chr7:18217980-18218363	GM12878	blood:	n/a	n/a
24	BHLHE40	chr7:18217930-18218221	GM12878	blood:	n/a	n/a
25	BHLHE40	chr7:18229222-18229524	GM12878	blood:	n/a	n/a
26	BHLHE40	chr7:18217461-18217661	GM12878	blood:	n/a	n/a
27	BHLHE40	chr7:18214755-18214817	K562	blood:	n/a	n/a
28	BHLHE40	chr7:18357060-18357405	K562	blood:	n/a	n/a
29	BHLHE40	chr7:18219765-18219857	K562	blood:	n/a	n/a
30	BHLHE40	chr7:18357066-18357374	HepG2	liver:	n/a	n/a
31	BHLHE40	chr7:18335718-18335912	GM12878	blood:	n/a	chr7:18335758-18335779 chr7:18335763-18335772
32	BHLHE40	chr7:18216983-18218305	K562	blood:	n/a	n/a
33	BRCA1	chr7:18357054-18357425	Hela-S3	cervix:	n/a	n/a
34	CBX3	chr7:18216792-18218313	K562	blood:	n/a	n/a
35	CBX3	chr7:18301664-18302173	HCT-116	colon:	n/a	n/a
36	CBX3	chr7:18274143-18274460	K562	blood:	n/a	n/a
37	CBX3	chr7:18214377-18214940	K562	blood:	n/a	n/a
38	CBX3	chr7:18277838-18278216	K562	blood:	n/a	n/a
39	CBX3	chr7:18217740-18218263	K562	blood:	n/a	n/a
40	CBX3	chr7:18217004-18217346	K562	blood:	n/a	n/a
41	CBX3	chr7:18301669-18302135	K562	blood:	n/a	n/a
42	CBX3	chr7:18301668-18302097	K562	blood:	n/a	n/a
43	CBX3	chr7:18301694-18302044	HCT-116	colon:	n/a	n/a
44	CBX3	chr7:18214475-18214818	K562	blood:	n/a	n/a
45	CCNT2	chr7:18360724-18360924	K562	blood:	n/a	n/a
46	CCNT2	chr7:18216722-18218280	K562	blood:	n/a	n/a
47	CCNT2	chr7:18215800-18216153	K562	blood:	n/a	n/a
48	CEBPB	chr7:18356868-18357405	IMR90	lung:	n/a	n/a
49	CEBPB	chr7:18217861-18218255	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr7:18205657-18205974	A549	lung:	n/a	chr7:18205808-18205819 chr7:18205807-18205818 chr7:18205807-18205818 chr7:18205809-18205818 chr7:18205809-18205818 chr7:18205807-18205820 chr7:18205809-18205818 chr7:18205809-18205818 chr7:18205807-18205820 chr7:18205807-18205820

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:18357830-18357880	GM12878	blood:	n/a
2	chr7:18330092-18330142	HNPCEpiC	eye:	n/a
3	chr7:18329562-18329612	NHBE	bronchial:	n/a
4	chr7:18329602-18329652	MCF10A-Er-Src	breast:	n/a
5	chr7:18329562-18329612	ECC-1	luminal epithelium:	n/a
6	chr7:18329916-18329966	HRCEpiC	kidney:	n/a
7	chr7:18329916-18329966	MCF10A-Er-Src	breast:	n/a
8	chr7:18329916-18329966	AG09319	gingival:	n/a
9	chr7:18329562-18329612	CMK	blood:	n/a
10	chr7:18330092-18330142	SK-N-SH_RA	brain:	n/a
11	chr7:18329562-18329612	PFSK-1	brain:	n/a
12	chr7:18329602-18329652	GM12892	blood:	n/a
13	chr7:18330092-18330142	H1-hESC	embryonic stem cell:	embryo
14	chr7:18329602-18329652	HepG2	liver:	n/a
15	chr7:18329916-18329966	NT2-D1	testis:	n/a
16	chr7:18329562-18329612	HNPCEpiC	eye:	n/a
17	chr7:18357830-18357880	AG09309	skin:	n/a
18	chr7:18329562-18329612	GM12891	blood:	n/a
19	chr7:18329562-18329612	Hela-S3	cervix:	n/a
20	chr7:18329562-18329612	Jurkat	blood:	n/a
21	chr7:18329562-18329612	RPTEC	kidney:	n/a
22	chr7:18329916-18329966	Jurkat	blood:	n/a
23	chr7:18329602-18329652	MCF-7	breast:	n/a
24	chr7:18329562-18329612	NH-A	brain:	n/a
25	chr7:18329602-18329652	CMK	blood:	n/a
26	chr7:18357830-18357880	Caco-2	colon:	n/a
27	chr7:18329602-18329652	HCM	heart:	n/a
28	chr7:18357830-18357880	T-47D	breast:	n/a
29	chr7:18329562-18329612	MCF10A-Er-Src	breast:	n/a
30	chr7:18329562-18329612	HAEpiC	amniotic membrane:	n/a
31	chr7:18330092-18330142	HEK293	kidney:	embryo
32	chr7:18357830-18357880	K562	blood:	n/a
33	chr7:18329562-18329612	BJ	skin:	n/a
34	chr7:18329916-18329966	GM06990	blood:	n/a
35	chr7:18329916-18329966	HepG2	liver:	n/a
36	chr7:18329916-18329966	AG09309	skin:	n/a
37	chr7:18329602-18329652	NHBE	bronchial:	n/a
38	chr7:18357830-18357880	SKMC	muscle:	n/a
39	chr7:18329602-18329652	HPAEpiC	pulmonary alveolar:	n/a
40	chr7:18330092-18330142	K562	blood:	n/a
41	chr7:18329562-18329612	ProgFib	skin:	n/a
42	chr7:18330092-18330142	SK-N-SH	brain:	n/a
43	chr7:18357830-18357880	HRCEpiC	kidney:	n/a
44	chr7:18329916-18329966	HL-60	blood:	n/a
45	chr7:18329916-18329966	HCT-116	colon:	n/a
46	chr7:18329562-18329612	AG10803	skin:	n/a
47	chr7:18329916-18329966	AoSMC	blood vessel:	n/a
48	chr7:18329916-18329966	GM19239	blood:	n/a
49	chr7:18329562-18329612	GM19239	blood:	n/a
50	chr7:18357830-18357880	HEK293	kidney:	embryo

(count:94 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:18311330..18313091-chr7:18314736..18317305,2	K562	blood:
2	chr7:18233266..18236170-chr7:18243676..18245578,2	K562	blood:
3	chr7:17245836..17248500-chr7:18215738..18217248,2	K562	blood:
4	chr7:18217240..18219162-chr7:18248697..18251214,2	MCF-7	breast:
5	chr7:18285766..18287431-chr7:18290399..18292754,2	MCF-7	breast:
6	chr7:18218172..18221072-chr7:18227014..18228909,2	K562	blood:
7	chr7:18311330..18313091-chr7:18314736..18317305,2	K562	blood:
8	chr7:18222330..18224720-chr7:18264492..18267054,2	K562	blood:
9	chr7:18223655..18225400-chr7:18230863..18233752,2	K562	blood:
10	chr7:18283780..18285456-chr7:18285459..18288294,2	K562	blood:
11	chr7:17746083..17746632-chr7:18359954..18360927,2	MCF-7	breast:
12	chr7:18010695..18011460-chr7:18360393..18361102,3	MCF-7	breast:
13	chr7:18236690..18239423-chr7:18240922..18243186,4	K562	blood:
14	chr7:18162840..18165489-chr7:18245304..18246939,2	K562	blood:
15	chr7:18205313..18207419-chr7:18215960..18218809,2	K562	blood:
16	chr7:18338973..18341007-chr7:18351398..18353885,2	K562	blood:
17	chr7:18285502..18287051-chr7:18294560..18297102,2	MCF-7	breast:
18	chr7:18223655..18225400-chr7:18230863..18233752,2	K562	blood:
19	chr7:18254427..18256952-chr7:18257278..18259018,2	K562	blood:
20	chr7:18217240..18219162-chr7:18248697..18251214,2	MCF-7	breast:
21	chr7:18354053..18356213-chr7:18358057..18360963,3	K562	blood:
22	chr7:18215961..18218185-chr7:18229835..18233297,4	K562	blood:
23	chr7:18254922..18255723-chr7:18360545..18361137,3	MCF-7	breast:
24	chr7:18206006..18208720-chr7:18214404..18217269,2	K562	blood:
25	chr7:18234357..18236170-chr7:18244078..18246116,2	K562	blood:
26	chr7:18254922..18255723-chr7:18360545..18361137,3	MCF-7	breast:
27	chr7:18216175..18219315-chr7:18243152..18247014,4	K562	blood:
28	chr7:18224613..18227615-chr7:18227879..18232094,3	K562	blood:
29	chr7:18162960..18165291-chr7:18262204..18264807,2	K562	blood:
30	chr7:18217795..18220211-chr7:18222403..18225204,2	MCF-7	breast:
31	chr7:18237325..18238963-chr7:18240694..18242384,2	MCF-7	breast:
32	chr7:18240899..18244580-chr7:18250175..18254118,3	K562	blood:
33	chr7:18234357..18236170-chr7:18244078..18246116,2	K562	blood:
34	chr7:18216175..18219315-chr7:18243152..18247014,4	K562	blood:
35	chr7:18222330..18224720-chr7:18264492..18267054,2	K562	blood:
36	chr7:18321787..18324563-chr7:18327488..18329360,2	K562	blood:
37	chr7:17978417..17980205-chr7:18243812..18246469,2	K562	blood:
38	chr7:18250651..18253317-chr7:18302876..18305651,2	K562	blood:
39	chr7:18215961..18218185-chr7:18229835..18233297,4	K562	blood:
40	chr7:18236690..18239423-chr7:18240922..18243186,4	K562	blood:
41	chr7:18251666..18253931-chr7:18265138..18267912,2	K562	blood:
42	chr7:18205313..18207419-chr7:18215960..18218809,2	K562	blood:
43	chr7:18218078..18219602-chr7:18220654..18223400,2	K562	blood:
44	chr7:18285502..18287051-chr7:18294560..18297102,2	MCF-7	breast:
45	chr7:18255243..18258028-chr7:18260325..18261899,2	MCF-7	breast:
46	chr7:18283780..18285456-chr7:18285459..18288294,2	K562	blood:
47	chr7:17977337..17980448-chr7:18216760..18219646,3	K562	blood:
48	chr7:17809237..17810176-chr7:18360328..18361291,2	MCF-7	breast:
49	chr7:18216226..18218726-chr7:18250746..18252267,2	K562	blood:
50	chr7:18237325..18238963-chr7:18240694..18242384,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AHR-8	chr7:18365135-18365215	NONHSAT119358
2	lnc-AHR-8	chr7:18367072-18367235	NONHSAT119358
3	lnc-AHR-8	chr7:18367072-18367381	NONHSAT119359
4	lnc-AHR-8	chr7:18330064-18330138	NONHSAT119359
5	lnc-AHR-8	chr7:18365135-18365215	NONHSAT119359
6	lnc-AHR-8	chr7:18329811-18329970	NONHSAT119359
7	lnc-AHR-8	chr7:18330073-18330138	NONHSAT119360

No data

Variant related genes	Relation type
ENSG00000223030	TF binding region
HDAC9	TF binding region
ENSG00000223030	CpG island
HDAC9	CpG island
ENSG00000071189	chromatin interactions
ENSG00000136261	chromatin interactions

Extended variants
information (count: 5736 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:5736 , 50 per page) page: 1 2 3 4 5 6 7 ... 115

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1160299	chr7:18205779-18205780	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs370129442	chr7:18205784-18205785	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs554729319	chr7:18205795-18205796	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs569822998	chr7:18205816-18205817	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs181899786	chr7:18205872-18205873	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs148672652	chr7:18205910-18205911	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs551110973	chr7:18205928-18205929	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs577207621	chr7:18205929-18205930	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs570865756	chr7:18205930-18205931	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs540995259	chr7:18205938-18205939	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs73062429	chr7:18205943-18205944	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs78302506	chr7:18205990-18205991	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs543079391	chr7:18206006-18206007	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs112269893	chr7:18206026-18206027	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs561048484	chr7:18206030-18206031	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs531749280	chr7:18206095-18206096	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs113200317	chr7:18206096-18206097	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs187219652	chr7:18206129-18206130	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs543597720	chr7:18206141-18206142	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs557201424	chr7:18206166-18206167	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs142320273	chr7:18206178-18206179	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs532816810	chr7:18206220-18206221	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs190782449	chr7:18206241-18206242	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs115150936	chr7:18206296-18206297	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs571131490	chr7:18206339-18206340	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs565644244	chr7:18206375-18206376	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs529662557	chr7:18206381-18206382	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs180756754	chr7:18206395-18206396	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs73317805	chr7:18206422-18206423	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs151286019	chr7:18206430-18206431	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs558763221	chr7:18206441-18206442	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs560402605	chr7:18206622-18206623	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534885153	chr7:18206668-18206669	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs553013289	chr7:18206681-18206682	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs572357591	chr7:18206705-18206706	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs574466345	chr7:18206721-18206722	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs536576400	chr7:18206770-18206771	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs186397921	chr7:18206776-18206777	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs367639626	chr7:18206809-18206810	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs533107412	chr7:18206817-18206818	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs576122795	chr7:18206819-18206820	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs200039756	chr7:18206831-18206832	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs190052193	chr7:18206835-18206836	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs573404088	chr7:18206838-18206839	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs182988620	chr7:18206849-18206850	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs545436827	chr7:18206868-18206869	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs376383336	chr7:18206870-18206871	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs541666424	chr7:18206928-18206929	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs559806225	chr7:18206962-18206963	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs530468124	chr7:18206965-18206966	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Rubinstein-Taybi syndrome	22470819	CNVD
Alzheimer''s disease	22166940	CNVD
Abnormal phenotypes	18644119	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Bladder cancer	21909424	CNVD
Cancer	21183584	CNVD
Autism	20808228	CNVD
Sezary syndrome	18413736	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:767 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:18192200-18207400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr7:18202600-18206600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr7:18203000-18214800	Weak transcription	Left Ventricle	heart
4	chr7:18203400-18207200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr7:18206600-18207400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr7:18207200-18207600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr7:18207400-18207600	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr7:18207600-18208400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr7:18214400-18214600	Enhancers	Right Atrium	heart
10	chr7:18214400-18215000	Enhancers	K562	blood
11	chr7:18214400-18215200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr7:18214400-18215200	Enhancers	Primary B cells from peripheral blood	blood
13	chr7:18214400-18215200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
14	chr7:18214600-18215000	Enhancers	Spleen	Spleen
15	chr7:18214800-18215000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr7:18214800-18215200	Enhancers	Placenta	Placenta
17	chr7:18214800-18215200	Enhancers	Left Ventricle	heart
18	chr7:18214800-18216200	Enhancers	HepG2	liver
19	chr7:18215000-18215200	Flanking Active TSS	K562	blood
20	chr7:18215000-18216000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr7:18215000-18216200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr7:18215000-18217200	Weak transcription	Spleen	Spleen
23	chr7:18215200-18215400	Enhancers	K562	blood
24	chr7:18215200-18217000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr7:18215200-18217000	Weak transcription	Primary B cells from peripheral blood	blood
26	chr7:18215200-18217000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr7:18215200-18217000	Weak transcription	Left Ventricle	heart
28	chr7:18215400-18215800	Enhancers	A549	lung
29	chr7:18215400-18216000	Enhancers	NH-A	brain
30	chr7:18215400-18216200	Flanking Active TSS	K562	blood
31	chr7:18215400-18216400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr7:18215400-18218200	Enhancers	Fetal Heart	heart
33	chr7:18215600-18216000	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr7:18215600-18216400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr7:18215600-18216400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr7:18215600-18216600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr7:18215600-18219200	Enhancers	Hela-S3	cervix
38	chr7:18215800-18216000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr7:18215800-18216000	Enhancers	Primary hematopoietic stem cells	blood
40	chr7:18215800-18216000	Flanking Active TSS	A549	lung
41	chr7:18215800-18216200	Enhancers	Fetal Intestine Small	intestine
42	chr7:18215800-18217200	Enhancers	Primary neutrophils fromperipheralblood	blood
43	chr7:18215800-18219200	Enhancers	Stomach Mucosa	stomach
44	chr7:18216000-18216400	Active TSS	A549	lung
45	chr7:18216000-18217000	Weak transcription	Primary hematopoietic stem cells	blood
46	chr7:18216000-18221000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr7:18216200-18216600	Active TSS	K562	blood
48	chr7:18216200-18217200	Weak transcription	HepG2	liver
49	chr7:18216200-18217600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr7:18216400-18216600	Flanking Active TSS	A549	lung

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