Variant report

Variant	esv16065
Chromosome Location	chr7:153106266-153111170
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:292)
CpG islands
(count:490)
Chromatin interactive
region (count:41)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:292 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:153109096-153109296	K562	blood:	n/a	n/a
2	ARID3A	chr7:153109739-153110062	K562	blood:	n/a	n/a
3	ARID3A	chr7:153110322-153112174	K562	blood:	n/a	n/a
4	ARID3A	chr7:153108540-153108589	K562	blood:	n/a	n/a
5	ATF1	chr7:153110923-153111307	K562	blood:	n/a	n/a
6	BACH1	chr7:153110739-153112141	K562	blood:	n/a	n/a
7	BACH1	chr7:153111122-153111267	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr7:153108498-153108636	K562	blood:	n/a	n/a
9	BACH1	chr7:153109751-153110110	K562	blood:	n/a	n/a
10	BCL3	chr7:153109499-153110250	K562	blood:	n/a	n/a
11	BCL3	chr7:153105524-153106503	K562	blood:	n/a	n/a
12	BCLAF1	chr7:153110402-153111174	K562	blood:	n/a	n/a
13	BCLAF1	chr7:153105443-153107677	K562	blood:	n/a	n/a
14	BCLAF1	chr7:153107687-153111130	K562	blood:	n/a	n/a
15	BHLHE40	chr7:153108552-153108560	K562	blood:	n/a	n/a
16	BHLHE40	chr7:153110425-153112117	K562	blood:	n/a	n/a
17	BHLHE40	chr7:153109125-153109401	K562	blood:	n/a	n/a
18	BHLHE40	chr7:153105622-153106329	K562	blood:	n/a	n/a
19	BHLHE40	chr7:153109730-153110195	K562	blood:	n/a	n/a
20	CBX3	chr7:153105517-153106346	K562	blood:	n/a	n/a
21	CBX3	chr7:153109631-153111793	K562	blood:	n/a	n/a
22	CBX3	chr7:153109019-153109556	K562	blood:	n/a	n/a
23	CBX3	chr7:153109704-153110153	K562	blood:	n/a	n/a
24	CBX3	chr7:153106552-153107270	K562	blood:	n/a	n/a
25	CBX3	chr7:153110381-153111716	K562	blood:	n/a	n/a
26	CBX3	chr7:153105511-153106312	K562	blood:	n/a	n/a
27	CCNT2	chr7:153105506-153106579	K562	blood:	n/a	n/a
28	CEBPB	chr7:153105854-153106412	K562	blood:	n/a	n/a
29	CEBPB	chr7:153109639-153110206	K562	blood:	n/a	n/a
30	CEBPB	chr7:153107799-153107824	K562	blood:	n/a	n/a
31	CEBPB	chr7:153106072-153106343	HepG2	liver:	n/a	n/a
32	CEBPB	chr7:153110588-153111609	K562	blood:	n/a	n/a
33	CEBPB	chr7:153105418-153106539	K562	blood:	n/a	n/a
34	CEBPB	chr7:153109256-153109540	K562	blood:	n/a	n/a
35	CEBPB	chr7:153110775-153111926	K562	blood:	n/a	chr7:153111856-153111867
36	CEBPB	chr7:153106100-153106367	IMR90	lung:	n/a	n/a
37	CEBPB	chr7:153106078-153106299	K562	blood:	n/a	n/a
38	CEBPD	chr7:153105628-153106466	K562	blood:	n/a	n/a
39	CEBPD	chr7:153106512-153107596	K562	blood:	n/a	n/a
40	CEBPD	chr7:153105380-153106455	K562	blood:	n/a	n/a
41	CEBPD	chr7:153110292-153111346	K562	blood:	n/a	n/a
42	CEBPD	chr7:153107843-153108748	K562	blood:	n/a	n/a
43	CHD2	chr7:153108045-153108482	K562	blood:	n/a	n/a
44	CHD2	chr7:153108792-153111309	K562	blood:	n/a	n/a
45	CHD2	chr7:153105569-153107151	K562	blood:	n/a	n/a
46	CREB1	chr7:153105710-153106335	K562	blood:	n/a	n/a
47	CREB1	chr7:153103133-153106882	K562	blood:	n/a	n/a
48	CTCF	chr7:153108119-153108164	Pancreas_OC	pancreas:	n/a	n/a
49	CTCF	chr7:153107011-153107336	K562	blood:	n/a	n/a
50	CTCF	chr7:153109442-153109480	GM10248	blood:	n/a	n/a

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:153109538-153109588	AoSMC	blood vessel:	n/a
2	chr7:153110762-153110812	AoSMC	blood vessel:	n/a
3	chr7:153109538-153109588	AoSMC	blood vessel:	n/a
4	chr7:153110762-153110812	AoSMC	blood vessel:	n/a
5	chr7:153108684-153108734	SAEC	small airway:	n/a
6	chr7:153109375-153109425	AG09309	skin:	n/a
7	chr7:153109375-153109425	K562	blood:	n/a
8	chr7:153110994-153111044	NHBE	bronchial:	n/a
9	chr7:153110492-153110542	NT2-D1	testis:	n/a
10	chr7:153108642-153108692	RPTEC	kidney:	n/a
11	chr7:153108726-153108776	HRE	kidney:	n/a
12	chr7:153109375-153109425	LNCaP	prostate:	n/a
13	chr7:153109375-153109425	NHDF-neo	bronchial:	n/a
14	chr7:153108684-153108734	HCPEpiC	choroid plexus:	n/a
15	chr7:153109538-153109588	SAEC	small airway:	n/a
16	chr7:153109375-153109425	SAEC	small airway:	n/a
17	chr7:153108726-153108776	AG09309	skin:	n/a
18	chr7:153110492-153110542	PFSK-1	brain:	n/a
19	chr7:153109375-153109425	HRPEpiC	eye:	n/a
20	chr7:153108642-153108692	GM06990	blood:	n/a
21	chr7:153109538-153109588	NHBE	bronchial:	n/a
22	chr7:153108726-153108776	K562	blood:	n/a
23	chr7:153109375-153109425	HCF	heart:	n/a
24	chr7:153110762-153110812	HEK293	kidney:	embryo
25	chr7:153108642-153108692	SK-N-SH	brain:	n/a
26	chr7:153108684-153108734	MCF-7	breast:	n/a
27	chr7:153110492-153110542	PrEC	prostate:	n/a
28	chr7:153108642-153108692	SKMC	muscle:	n/a
29	chr7:153108684-153108734	HPAEpiC	pulmonary alveolar:	n/a
30	chr7:153108642-153108692	CMK	blood:	n/a
31	chr7:153109538-153109588	CMK	blood:	n/a
32	chr7:153110994-153111044	ECC-1	luminal epithelium:	n/a
33	chr7:153110492-153110542	NHDF-neo	bronchial:	n/a
34	chr7:153108642-153108692	ovcar-3	ovarian:	n/a
35	chr7:153108642-153108692	AG09309	skin:	n/a
36	chr7:153108642-153108692	NB4	blood:	n/a
37	chr7:153109538-153109588	AG09309	skin:	n/a
38	chr7:153110762-153110812	SKMC	muscle:	n/a
39	chr7:153108726-153108776	HMEC	breast:	n/a
40	chr7:153110762-153110812	HRE	kidney:	n/a
41	chr7:153109538-153109588	BE2_C	brain:	n/a
42	chr7:153110994-153111044	HL-60	blood:	n/a
43	chr7:153110492-153110542	HIPEpiC	eye:	n/a
44	chr7:153108726-153108776	SK-N-SH	brain:	n/a
45	chr7:153110492-153110542	HRPEpiC	eye:	n/a
46	chr7:153108684-153108734	HUVEC	blood vessel:	n/a
47	chr7:153109375-153109425	HAEpiC	amniotic membrane:	n/a
48	chr7:153108684-153108734	GM12878	blood:	n/a
49	chr7:153110994-153111044	SK-N-SH	brain:	n/a
50	chr7:153110994-153111044	MCF-7	breast:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:5956902..5959926-chr7:153104101..153108228,8	K562	blood:
2	chr2:84104828..84106331-chr7:153109556..153111137,2	K562	blood:
3	chr7:152630894..152632696-chr7:153103935..153106331,2	K562	blood:
4	chr7:153104344..153107285-chr7:153206128..153208703,2	K562	blood:
5	chr7:153105650..153108822-chr7:153162776..153165855,3	K562	blood:
6	chr7:153104137..153106481-chr7:153366224..153368570,2	K562	blood:
7	chr7:153105266..153107285-chr7:153207203..153209217,2	K562	blood:
8	chr7:64299266..64299795-chr7:153109659..153110240,2	K562	blood:
9	chr7:153104593..153107356-chr7:153151532..153153946,4	K562	blood:
10	chr7:153103586..153106568-chr7:153587349..153589344,2	K562	blood:
11	chr7:153103747..153106321-chr7:153180376..153182318,2	K562	blood:
12	chr7:153018926..153020911-chr7:153105135..153106975,2	K562	blood:
13	chr7:153104280..153106430-chr7:153200479..153202606,2	K562	blood:
14	chr7:153105710..153107855-chr7:153165499..153167992,2	K562	blood:
15	chr7:153032299..153036856-chr7:153103737..153108075,4	K562	blood:
16	chr7:153102721..153106606-chr7:153212905..153219163,7	K562	blood:
17	chr7:153106993..153109091-chr7:153192344..153194750,2	K562	blood:
18	chr7:152160161..152162874-chr7:153109419..153112345,3	K562	blood:
19	chr11:5952222..5953725-chr7:153106291..153108525,3	K562	blood:
20	chr7:64297147..64300786-chr7:153106859..153112225,9	K562	blood:
21	chr2:84103331..84106345-chr7:153106704..153111137,6	K562	blood:
22	chr7:152615135..152617990-chr7:153104764..153107812,3	K562	blood:
23	chr11:5956902..5959925-chr7:153104319..153108206,5	K562	blood:
24	chr7:153029560..153032040-chr7:153105014..153106931,2	K562	blood:
25	chr7:153103693..153106480-chr7:153169343..153171365,2	K562	blood:
26	chr7:152886505..152888240-chr7:153106300..153108850,2	K562	blood:
27	chr7:153104483..153106622-chr7:154809652..154811276,2	K562	blood:
28	chr1:113496225..113498697-chr7:153107803..153110252,2	K562	blood:
29	chr7:153106936..153109083-chr7:153612449..153615319,2	K562	blood:
30	chr7:64297147..64300763-chr7:153106859..153112373,8	K562	blood:
31	chr7:152932848..152935225-chr7:153105144..153107809,2	K562	blood:
32	chr7:153103866..153106849-chr7:153334968..153337420,2	K562	blood:
33	chr7:153103427..153106418-chr7:153612695..153615251,3	K562	blood:
34	chr7:152589505..152592233-chr7:153104803..153106680,2	K562	blood:
35	chr7:153104450..153106704-chr7:153631945..153634979,3	K562	blood:
36	chr20:34540044..34543008-chr7:153104982..153106746,2	K562	blood:
37	chr7:152600593..152604431-chr7:153104940..153107829,3	K562	blood:
38	chr7:152947748..152949504-chr7:153104988..153107669,2	K562	blood:
39	chr7:153052023..153054684-chr7:153104200..153106325,2	K562	blood:
40	chr7:153103375..153106774-chr7:153173661..153176724,3	K562	blood:
41	chr7:153103413..153106356-chr7:153237101..153239788,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-XRCC2-1	chr7:153110698-153111021	ENSG00000234722
2	lnc-XRCC2-1	chr7:153109178-153109319	ENSG00000234722
3	lnc-XRCC2-1	chr7:153109176-153109319	ENSG00000234722.3

No data

Variant related genes	Relation type
ENSG00000234722	TF binding region
ENSG00000234722	CpG island
ENSG00000261455	chromatin interactions
ENSG00000155380	chromatin interactions
ENSG00000171222	chromatin interactions
ENSG00000234338	chromatin interactions
ENSG00000236198	chromatin interactions
ENSG00000223700	chromatin interactions
ENSG00000132256	chromatin interactions

Extended variants
information (count: 313 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:313 , 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	rs117328137	chr7:153106269-153106270	Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs570535119	chr7:153106270-153106271	Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs554542367	chr7:153106279-153106280	Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs576005039	chr7:153106280-153106281	Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs368651832	chr7:153106362-153106363	Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs371811575	chr7:153106389-153106390	Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs375361802	chr7:153106393-153106394	Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs192862242	chr7:153106482-153106483	Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs540850630	chr7:153106518-153106519	Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs141129040	chr7:153106531-153106532	Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs534662925	chr7:153106552-153106553	Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs577996673	chr7:153106564-153106565	Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs150297196	chr7:153106565-153106566	Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs548431382	chr7:153106587-153106588	Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs59683680	chr7:153106606-153106607	Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs530814016	chr7:153106609-153106610	Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs552795972	chr7:153106634-153106635	Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs75845881	chr7:153106642-153106643	Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs571176227	chr7:153106643-153106644	Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs535200509	chr7:153106658-153106659	Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs114892779	chr7:153106680-153106681	Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs138311273	chr7:153106737-153106738	Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs185056116	chr7:153106768-153106769	Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs57142255	chr7:153106784-153106785	Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs546696869	chr7:153106798-153106799	Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs189528612	chr7:153106819-153106820	Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs536666327	chr7:153106917-153106918	Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs368052898	chr7:153106924-153106925	Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs558404509	chr7:153106997-153106998	Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs114015945	chr7:153107028-153107029	Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs181835213	chr7:153107031-153107032	Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs112881772	chr7:153107032-153107033	Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs113676535	chr7:153107044-153107045	Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs386719645	chr7:153107059-153107060	Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs369725624	chr7:153107073-153107074	Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs368701637	chr7:153107098-153107099	Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs183826928	chr7:153107121-153107122	Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs189133061	chr7:153107144-153107145	Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs181588624	chr7:153107145-153107146	Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs114455134	chr7:153107196-153107197	Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs564499124	chr7:153107220-153107221	Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs528787645	chr7:153107245-153107246	Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs115102655	chr7:153107317-153107318	Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs536090985	chr7:153107330-153107331	Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs147334602	chr7:153107332-153107333	Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs56347380	chr7:153107359-153107360	Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs575928022	chr7:153107387-153107388	Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs374890275	chr7:153107390-153107391	Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs569675420	chr7:153107400-153107401	Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs537179230	chr7:153107402-153107403	Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
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
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	16864856	CNVD
Autism	20808228	CNVD
Ovarian cancer	21720365	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Autism	22102821	CNVD
Myelofibrosis	22110671	CNVD
Nasopharyngeal cancer	20548289	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:153105800-153106800	Genic enhancers	K562	blood
2	chr7:153106800-153110000	Transcr. at gene 5' and 3'	K562	blood
3	chr7:153110000-153111000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr7:153110000-153111400	Active TSS	K562	blood

The 2.0 version of rSNPBase

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