Variant report

Variant	nsv971157
Chromosome Location	chr7:100143688-100148402
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:486)
CpG islands
(count:61)
Chromatin interactive
region (count:34)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:486 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:100143215-100144723	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:100144203-100144803	K562	blood:	n/a	n/a
3	ATF2	chr7:100144090-100144684	GM12878	blood:	n/a	n/a
4	ATF2	chr7:100143039-100143755	GM12878	blood:	n/a	n/a
5	ATF2	chr7:100142852-100143792	GM12878	blood:	n/a	n/a
6	ATF3	chr7:100143221-100143702	K562	blood:	n/a	n/a
7	ATF3	chr7:100142993-100143750	A549	lung:	n/a	n/a
8	ATF3	chr7:100145618-100145871	K562	blood:	n/a	n/a
9	BACH1	chr7:100145276-100145402	K562	blood:	n/a	n/a
10	BATF	chr7:100142987-100143755	GM12878	blood:	n/a	chr7:100143382-100143392
11	BATF	chr7:100143079-100143703	GM12878	blood:	n/a	chr7:100143382-100143392
12	BATF	chr7:100144505-100144849	GM12878	blood:	n/a	chr7:100144692-100144701 chr7:100144712-100144723
13	BCL11A	chr7:100143323-100143704	GM12878	blood:	n/a	n/a
14	BCL11A	chr7:100143002-100143744	GM12878	blood:	n/a	n/a
15	BCL3	chr7:100143039-100144262	A549	lung:	n/a	chr7:100144045-100144054 chr7:100143781-100143794 chr7:100143785-100143798
16	BCL3	chr7:100142866-100143776	A549	lung:	n/a	n/a
17	BCLAF1	chr7:100143195-100143772	GM12878	blood:	n/a	n/a
18	BCLAF1	chr7:100142905-100143797	GM12878	blood:	n/a	chr7:100143781-100143794
19	BHLHE40	chr7:100143954-100144151	K562	blood:	n/a	n/a
20	BHLHE40	chr7:100148132-100148196	GM12878	blood:	n/a	n/a
21	BHLHE40	chr7:100143838-100144274	HepG2	liver:	n/a	n/a
22	BHLHE40	chr7:100145426-100145926	K562	blood:	n/a	chr7:100145736-100145757
23	BHLHE40	chr7:100143160-100143690	GM12878	blood:	n/a	n/a
24	BHLHE40	chr7:100143920-100144227	HepG2	liver:	n/a	n/a
25	BHLHE40	chr7:100143934-100144533	GM12878	blood:	n/a	n/a
26	BHLHE40	chr7:100145494-100145921	GM12878	blood:	n/a	chr7:100145736-100145757
27	CBX3	chr7:100143199-100143814	K562	blood:	n/a	n/a
28	CEBPB	chr7:100143394-100143739	IMR90	lung:	n/a	n/a
29	CEBPB	chr7:100143108-100144319	A549	lung:	n/a	n/a
30	CEBPB	chr7:100143279-100144164	HepG2	liver:	n/a	n/a
31	CEBPB	chr7:100143251-100143759	A549	lung:	n/a	n/a
32	CEBPB	chr7:100143302-100143750	A549	lung:	n/a	n/a
33	CEBPB	chr7:100142912-100144127	GM12878	blood:	n/a	n/a
34	CEBPB	chr7:100142642-100143702	Hela-S3	cervix:	n/a	n/a
35	CEBPD	chr7:100143199-100143707	HepG2	liver:	n/a	n/a
36	CHD1	chr7:100145215-100145711	GM12878	blood:	n/a	n/a
37	CHD2	chr7:100143247-100143735	GM12878	blood:	n/a	n/a
38	CHD2	chr7:100144863-100144935	K562	blood:	n/a	n/a
39	CHD2	chr7:100143911-100143968	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr7:100143220-100143715	Hela-S3	cervix:	n/a	n/a
41	CHD2	chr7:100143963-100144900	GM12878	blood:	n/a	n/a
42	CREB1	chr7:100143237-100143891	A549	lung:	n/a	n/a
43	CTCF	chr7:100145660-100145810	AG04449	skin:	n/a	n/a
44	CTCF	chr7:100145680-100145830	HMF	breast:	n/a	n/a
45	CTCF	chr7:100144200-100144350	GM12870	blood:	n/a	n/a
46	CTCF	chr7:100145640-100145790	GM12875	blood:	n/a	n/a
47	CTCF	chr7:100145660-100145810	AG04450	lung:	n/a	n/a
48	CTCF	chr7:100145680-100145830	HPF	lung:	n/a	n/a
49	CTCF	chr7:100144440-100144590	GM12864	blood:	n/a	n/a
50	CTCF	chr7:100143480-100143710	HCM	heart:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:100144475-100144525	GM12891	blood:	n/a
2	chr7:100144475-100144525	CMK	blood:	n/a
3	chr7:100144475-100144525	AG09309	skin:	n/a
4	chr7:100144475-100144525	GM12892	blood:	n/a
5	chr7:100144475-100144525	T-47D	breast:	n/a
6	chr7:100144475-100144525	NH-A	brain:	n/a
7	chr7:100144475-100144525	HCF	heart:	n/a
8	chr7:100144475-100144525	SAEC	small airway:	n/a
9	chr7:100144475-100144525	HEK293	kidney:	embryo
10	chr7:100144475-100144525	Caco-2	colon:	n/a
11	chr7:100144475-100144525	SK-N-MC	brain:	n/a
12	chr7:100144475-100144525	IMR90	lung:	fetal
13	chr7:100144475-100144525	AG09319	gingival:	n/a
14	chr7:100144475-100144525	ovcar-3	ovarian:	n/a
15	chr7:100144475-100144525	HPAEpiC	pulmonary alveolar:	n/a
16	chr7:100144475-100144525	HRCEpiC	kidney:	n/a
17	chr7:100144475-100144525	H1-hESC	embryonic stem cell:	embryo
18	chr7:100144475-100144525	GM06990	blood:	n/a
19	chr7:100144475-100144525	PrEC	prostate:	n/a
20	chr7:100144475-100144525	NHDF-neo	bronchial:	n/a
21	chr7:100144475-100144525	HL-60	blood:	n/a
22	chr7:100144475-100144525	BE2_C	brain:	n/a
23	chr7:100144475-100144525	SK-N-SH_RA	brain:	n/a
24	chr7:100144475-100144525	HAEpiC	amniotic membrane:	n/a
25	chr7:100144475-100144525	ProgFib	skin:	n/a
26	chr7:100144475-100144525	AG04450	lung:	fetal
27	chr7:100144475-100144525	AG10803	skin:	n/a
28	chr7:100144475-100144525	HCPEpiC	choroid plexus:	n/a
29	chr7:100144475-100144525	AoSMC	blood vessel:	n/a
30	chr7:100144475-100144525	NB4	blood:	n/a
31	chr7:100144475-100144525	GM19239	blood:	n/a
32	chr7:100144475-100144525	Hepatocyte	liver:	n/a
33	chr7:100144475-100144525	BJ	skin:	n/a
34	chr7:100144475-100144525	HUVEC	blood vessel:	n/a
35	chr7:100144475-100144525	HCT-116	colon:	n/a
36	chr7:100144475-100144525	U87	brain:	n/a
37	chr7:100144475-100144525	HIPEpiC	eye:	n/a
38	chr7:100144475-100144525	ECC-1	luminal epithelium:	n/a
39	chr7:100144475-100144525	HCM	heart:	n/a
40	chr7:100144475-100144525	NHBE	bronchial:	n/a
41	chr7:100144475-100144525	A549	lung:	n/a
42	chr7:100144475-100144525	HEEpiC	esophagus:	n/a
43	chr7:100144475-100144525	LNCaP	prostate:	n/a
44	chr7:100144475-100144525	GM12878	blood:	n/a
45	chr7:100144475-100144525	AG04449	skin:	fetal
46	chr7:100144475-100144525	SK-N-SH	brain:	n/a
47	chr7:100144475-100144525	HRE	kidney:	n/a
48	chr7:100144475-100144525	HepG2	liver:	n/a
49	chr7:100144475-100144525	HMEC	breast:	n/a
50	chr7:100144475-100144525	HRPEpiC	eye:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:100143139..100144960-chr7:100210042..100212066,2	K562	blood:
2	chr7:100143448..100145792-chr7:100271668..100273446,2	MCF-7	breast:
3	chr7:100144895..100147255-chr7:100148488..100151702,4	K562	blood:
4	chr7:100063079..100063989-chr7:100144215..100144855,2	K562	blood:
5	chr7:100032414..100033926-chr7:100144081..100145594,2	K562	blood:
6	chr7:100145206..100146855-chr7:100182658..100185253,2	K562	blood:
7	chr7:100146512..100148018-chr7:100154524..100156081,2	K562	blood:
8	chr7:100074335..100078343-chr7:100142686..100146158,4	K562	blood:
9	chr7:100140502..100142594-chr7:100143525..100145435,2	K562	blood:
10	chr7:100067039..100069939-chr7:100143624..100146249,2	K562	blood:
11	chr7:100030016..100034371-chr7:100142404..100146654,4	K562	blood:
12	chr7:100145746..100147750-chr7:100180240..100183063,2	K562	blood:
13	chr7:100080527..100083060-chr7:100141951..100145813,4	MCF-7	breast:
14	chr7:100076149..100078056-chr7:100145849..100148358,2	MCF-7	breast:
15	chr7:100061179..100064174-chr7:100142054..100143919,2	K562	blood:
16	chr7:100142950..100145314-chr7:100161125..100163240,2	K562	blood:
17	chr7:100025997..100028505-chr7:100141449..100143721,2	MCF-7	breast:
18	chr7:100136291..100139067-chr7:100140246..100145508,4	MCF-7	breast:
19	chr7:100143245..100145713-chr7:100199778..100203079,3	MCF-7	breast:
20	chr7:100140983..100146932-chr7:100182357..100186194,10	MCF-7	breast:
21	chr7:100025881..100027667-chr7:100143251..100146330,4	MCF-7	breast:
22	chr7:100025634..100027530-chr7:100143526..100145489,2	K562	blood:
23	chr7:100145586..100147127-chr7:100152126..100154333,2	K562	blood:
24	chr7:100065337..100067606-chr7:100143752..100145766,2	MCF-7	breast:
25	chr7:100142335..100144694-chr7:100146748..100149510,3	K562	blood:
26	chr7:100034086..100036624-chr7:100146945..100148605,2	K562	blood:
27	chr7:100144116..100146517-chr7:100289943..100291876,2	K562	blood:
28	chr7:100144343..100147077-chr7:100156607..100158371,2	MCF-7	breast:
29	chr7:100142841..100146326-chr7:100160207..100163065,3	MCF-7	breast:
30	chr7:100141487..100144211-chr7:100154594..100158320,3	MCF-7	breast:
31	chr7:100143577..100145211-chr7:100180031..100182996,2	K562	blood:
32	chr7:100024941..100027622-chr7:100141781..100145026,4	K562	blood:
33	chr7:100142903..100145091-chr7:100168075..100170895,2	MCF-7	breast:
34	chr7:100142201..100145553-chr7:100159344..100161288,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRCH4-3	chr7:100144031-100144165	NONHSAT122385

No data

Variant related genes	Relation type
AGFG2	TF binding region
AGFG2	CpG island
ENSG00000146834	chromatin interactions
ENSG00000166924	chromatin interactions
ENSG00000241357	chromatin interactions
ENSG00000160813	chromatin interactions
ENSG00000172354	chromatin interactions
ENSG00000240211	chromatin interactions
ENSG00000077454	chromatin interactions
ENSG00000106336	chromatin interactions
ENSG00000106330	chromatin interactions
ENSG00000266372	chromatin interactions
ENSG00000224729	chromatin interactions
ENSG00000078487	chromatin interactions
ENSG00000166925	chromatin interactions
ENSG00000106351	chromatin interactions
ENSG00000106333	chromatin interactions
ENSG00000185955	chromatin interactions

Extended variants
information (count: 180 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:180 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567119839	chr7:100143732-100143733	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
2	rs73407314	chr7:100143738-100143739	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	17 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs542581716	chr7:100143782-100143783	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
4	rs530123407	chr7:100143783-100143784	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
5	rs562109006	chr7:100143785-100143786	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
6	rs577914230	chr7:100143787-100143788	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
7	rs545335065	chr7:100143789-100143790	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
8	rs369808681	chr7:100143792-100143793	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
9	rs553908192	chr7:100143795-100143796	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
10	rs373347735	chr7:100143796-100143797	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
11	rs374054523	chr7:100143798-100143799	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
12	rs377324852	chr7:100143799-100143800	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
13	rs369480072	chr7:100143805-100143806	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
14	rs572604667	chr7:100143885-100143886	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
15	rs371874193	chr7:100143900-100143901	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
16	rs77600299	chr7:100143901-100143902	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
17	rs561448761	chr7:100143943-100143944	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
18	rs559736125	chr7:100143966-100143967	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
19	rs187579309	chr7:100143999-100144000	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
20	rs528471441	chr7:100144049-100144050	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	16 gene(s)	Overlapped CNVs	n/a
21	rs543817341	chr7:100144058-100144059	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	16 gene(s)	Overlapped CNVs	n/a
22	rs551863324	chr7:100144083-100144084	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	16 gene(s)	Overlapped CNVs	n/a
23	rs565322468	chr7:100144088-100144089	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	16 gene(s)	Overlapped CNVs	n/a
24	rs62482217	chr7:100144111-100144112	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	16 gene(s)	Overlapped CNVs	n/a
25	rs533253323	chr7:100144125-100144126	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	16 gene(s)	Overlapped CNVs	n/a
26	rs571617567	chr7:100144151-100144152	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	16 gene(s)	Overlapped CNVs	n/a
27	rs551708600	chr7:100144209-100144210	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
28	rs566498764	chr7:100144222-100144223	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
29	rs529309160	chr7:100144229-100144230	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
30	rs527498980	chr7:100144280-100144281	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
31	rs112088134	chr7:100144348-100144349	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
32	rs367600937	chr7:100144360-100144361	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
33	rs567336058	chr7:100144453-100144454	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
34	rs537598759	chr7:100144596-100144597	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
35	rs547781147	chr7:100144638-100144639	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
36	rs145050281	chr7:100144671-100144672	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
37	rs538900577	chr7:100144675-100144676	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
38	rs190708054	chr7:100144734-100144735	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
39	rs559840052	chr7:100144744-100144745	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
40	rs572511739	chr7:100144761-100144762	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
41	rs536836962	chr7:100144790-100144791	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
42	rs554892320	chr7:100144824-100144825	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
43	rs371359468	chr7:100144831-100144832	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
44	rs576475060	chr7:100144918-100144919	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
45	rs375814758	chr7:100144964-100144965	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
46	rs113004472	chr7:100145029-100145030	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
47	rs551257368	chr7:100145030-100145031	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
48	rs35296477	chr7:100145041-100145042	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
49	rs565236186	chr7:100145090-100145091	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
50	rs577312226	chr7:100145106-100145107	Enhancers Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
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
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	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
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Breast cancer	21509527	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:496 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100137800-100144000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
2	chr7:100137800-100146600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr7:100138000-100145400	Weak transcription	Primary B cells from cord blood	blood
4	chr7:100138000-100145400	Weak transcription	Fetal Brain Male	brain
5	chr7:100138000-100145400	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr7:100138200-100146400	Weak transcription	Fetal Brain Female	brain
7	chr7:100138400-100146400	Weak transcription	Dnd41	blood
8	chr7:100139200-100144600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr7:100140000-100144400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr7:100140000-100145800	Enhancers	Brain Inferior Temporal Lobe	brain
11	chr7:100140000-100148000	Enhancers	Primary B cells from peripheral blood	blood
12	chr7:100140400-100144000	Enhancers	K562	blood
13	chr7:100140400-100144600	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr7:100140400-100145400	Enhancers	H1 Cell Line	embryonic stem cell
15	chr7:100140400-100146200	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr7:100140600-100143800	Enhancers	Primary T cells fromperipheralblood	blood
17	chr7:100140600-100144600	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr7:100140600-100144800	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr7:100140600-100145400	Weak transcription	Gastric	stomach
20	chr7:100140800-100145000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
21	chr7:100141000-100144000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr7:100141000-100145800	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr7:100141000-100145800	Flanking Active TSS	GM12878-XiMat	blood
24	chr7:100141000-100146000	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr7:100141000-100146600	Enhancers	Brain Cingulate Gyrus	brain
26	chr7:100141200-100144200	Enhancers	Brain Hippocampus Middle	brain
27	chr7:100141200-100146200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
28	chr7:100141200-100146600	Enhancers	Small Intestine	intestine
29	chr7:100141400-100144200	Enhancers	Stomach Smooth Muscle	stomach
30	chr7:100141400-100144600	Enhancers	Brain Angular Gyrus	brain
31	chr7:100141600-100144200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr7:100141600-100144600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
33	chr7:100141600-100145400	Flanking Active TSS	A549	lung
34	chr7:100141600-100146200	Enhancers	Sigmoid Colon	Sigmoid Colon
35	chr7:100141600-100146400	Enhancers	Duodenum Smooth Muscle	Duodenum
36	chr7:100141600-100146600	Enhancers	Fetal Heart	heart
37	chr7:100141800-100144600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr7:100141800-100145400	Enhancers	Psoas Muscle	Psoas
39	chr7:100141800-100145600	Flanking Active TSS	Liver	Liver
40	chr7:100141800-100145600	Enhancers	Fetal Intestine Small	intestine
41	chr7:100141800-100145800	Enhancers	Fetal Intestine Large	intestine
42	chr7:100141800-100146200	Enhancers	Fetal Muscle Leg	muscle
43	chr7:100141800-100146400	Enhancers	Left Ventricle	heart
44	chr7:100141800-100146600	Enhancers	Adipose Nuclei	Adipose
45	chr7:100141800-100146600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr7:100141800-100147000	Enhancers	Right Atrium	heart
47	chr7:100141800-100147000	Enhancers	Stomach Mucosa	stomach
48	chr7:100142000-100143800	Enhancers	Brain Anterior Caudate	brain
49	chr7:100142000-100145400	Enhancers	Fetal Thymus	thymus
50	chr7:100142000-100145800	Enhancers	Skeletal Muscle Female	skeletal muscle

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