Variant report

Variant	nsv608057
Chromosome Location	chr7:102440184-102538515
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1375)
CpG islands
(count:428)
Chromatin interactive
region (count:62)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1375 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:102516155-102516615	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:102514028-102514887	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:102452449-102452773	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:102509524-102509951	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:102500720-102501319	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:102478846-102479241	HepG2	liver:	n/a	n/a
7	ATF1	chr7:102533184-102533443	K562	blood:	n/a	n/a
8	ATF1	chr7:102516353-102516642	K562	blood:	n/a	n/a
9	ATF1	chr7:102531030-102531406	K562	blood:	n/a	n/a
10	ATF2	chr7:102481620-102482163	GM12878	blood:	n/a	n/a
11	ATF2	chr7:102475399-102475848	GM12878	blood:	n/a	n/a
12	ATF2	chr7:102484177-102484790	GM12878	blood:	n/a	n/a
13	ATF2	chr7:102484200-102484713	GM12878	blood:	n/a	n/a
14	ATF2	chr7:102475368-102475893	GM12878	blood:	n/a	n/a
15	ATF3	chr7:102515996-102516786	A549	lung:	n/a	n/a
16	ATF3	chr7:102516058-102516843	HCT-116	colon:	n/a	n/a
17	ATF3	chr7:102516248-102516624	K562	blood:	n/a	n/a
18	ATF3	chr7:102515979-102516734	HCT-116	colon:	n/a	n/a
19	ATF3	chr7:102516084-102516739	A549	lung:	n/a	n/a
20	BATF	chr7:102481731-102482084	GM12878	blood:	n/a	n/a
21	BATF	chr7:102484252-102484610	GM12878	blood:	n/a	n/a
22	BATF	chr7:102484259-102484624	GM12878	blood:	n/a	n/a
23	BATF	chr7:102514586-102514859	GM12878	blood:	n/a	n/a
24	BATF	chr7:102514509-102514873	GM12878	blood:	n/a	n/a
25	BATF	chr7:102475426-102475852	GM12878	blood:	n/a	chr7:102475647-102475658 chr7:102475648-102475658
26	BATF	chr7:102481751-102482055	GM12878	blood:	n/a	n/a
27	BATF	chr7:102475444-102475777	GM12878	blood:	n/a	chr7:102475647-102475658 chr7:102475648-102475658
28	BCL11A	chr7:102484258-102484654	GM12878	blood:	n/a	n/a
29	BCL11A	chr7:102484332-102484641	GM12878	blood:	n/a	n/a
30	BCL11A	chr7:102514598-102514832	GM12878	blood:	n/a	chr7:102514741-102514750
31	BCL11A	chr7:102475497-102475744	GM12878	blood:	n/a	n/a
32	BCL11A	chr7:102475417-102475810	GM12878	blood:	n/a	n/a
33	BCL11A	chr7:102481679-102482030	GM12878	blood:	n/a	n/a
34	BCL3	chr7:102515964-102516936	A549	lung:	n/a	n/a
35	BCL3	chr7:102454575-102454898	GM12878	blood:	n/a	n/a
36	BCL3	chr7:102484358-102484686	GM12878	blood:	n/a	n/a
37	BCL3	chr7:102515891-102516752	A549	lung:	n/a	chr7:102515915-102515924
38	BCLAF1	chr7:102475385-102475792	GM12878	blood:	n/a	n/a
39	BCLAF1	chr7:102481611-102482122	GM12878	blood:	n/a	n/a
40	BCLAF1	chr7:102484307-102484685	GM12878	blood:	n/a	n/a
41	BHLHE40	chr7:102516444-102516605	K562	blood:	n/a	n/a
42	BHLHE40	chr7:102484310-102484623	GM12878	blood:	n/a	n/a
43	BHLHE40	chr7:102475416-102475745	GM12878	blood:	n/a	n/a
44	BRCA1	chr7:102516256-102516827	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr7:102531852-102531897	GM12878	blood:	n/a	n/a
46	CBX3	chr7:102516123-102516857	HCT-116	colon:	n/a	n/a
47	CBX3	chr7:102514418-102515075	HCT-116	colon:	n/a	n/a
48	CBX3	chr7:102515992-102516945	HCT-116	colon:	n/a	n/a
49	CBX3	chr7:102514409-102515051	HCT-116	colon:	n/a	n/a
50	CBX3	chr7:102475384-102475952	HCT-116	colon:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:102506387-102506437	GM12892	blood:	n/a
2	chr7:102506387-102506437	GM12892	blood:	n/a
3	chr7:102477205-102477255	NHBE	bronchial:	n/a
4	chr7:102470281-102470331	ProgFib	skin:	n/a
5	chr7:102453328-102453378	GM12892	blood:	n/a
6	chr7:102506387-102506437	ProgFib	skin:	n/a
7	chr7:102477205-102477255	PFSK-1	brain:	n/a
8	chr7:102477205-102477255	NT2-D1	testis:	n/a
9	chr7:102506387-102506437	Caco-2	colon:	n/a
10	chr7:102449340-102449390	GM12891	blood:	n/a
11	chr7:102449340-102449390	Hela-S3	cervix:	n/a
12	chr7:102453328-102453378	HL-60	blood:	n/a
13	chr7:102531568-102531618	HEK293	kidney:	embryo
14	chr7:102449340-102449390	T-47D	breast:	n/a
15	chr7:102500111-102500161	NHDF-neo	bronchial:	n/a
16	chr7:102506387-102506437	BJ	skin:	n/a
17	chr7:102453328-102453378	NH-A	brain:	n/a
18	chr7:102470281-102470331	GM19239	blood:	n/a
19	chr7:102506387-102506437	HPAEpiC	pulmonary alveolar:	n/a
20	chr7:102449340-102449390	HL-60	blood:	n/a
21	chr7:102477205-102477255	HCM	heart:	n/a
22	chr7:102500111-102500161	HEK293	kidney:	embryo
23	chr7:102449340-102449390	HEEpiC	esophagus:	n/a
24	chr7:102531568-102531618	SAEC	small airway:	n/a
25	chr7:102449340-102449390	HCT-116	colon:	n/a
26	chr7:102506387-102506437	Hela-S3	cervix:	n/a
27	chr7:102477205-102477255	GM12878	blood:	n/a
28	chr7:102531568-102531618	ProgFib	skin:	n/a
29	chr7:102470281-102470331	AG04449	skin:	fetal
30	chr7:102500111-102500161	AG04450	lung:	fetal
31	chr7:102449340-102449390	MCF10A-Er-Src	breast:	n/a
32	chr7:102449340-102449390	NHBE	bronchial:	n/a
33	chr7:102449340-102449390	GM06990	blood:	n/a
34	chr7:102449340-102449390	SAEC	small airway:	n/a
35	chr7:102453328-102453378	T-47D	breast:	n/a
36	chr7:102449340-102449390	NH-A	brain:	n/a
37	chr7:102449340-102449390	CMK	blood:	n/a
38	chr7:102500111-102500161	HAEpiC	amniotic membrane:	n/a
39	chr7:102449340-102449390	HPAEpiC	pulmonary alveolar:	n/a
40	chr7:102470281-102470331	NHBE	bronchial:	n/a
41	chr7:102453328-102453378	SK-N-SH	brain:	n/a
42	chr7:102449340-102449390	ProgFib	skin:	n/a
43	chr7:102449340-102449390	SK-N-SH	brain:	n/a
44	chr7:102453328-102453378	GM06990	blood:	n/a
45	chr7:102477205-102477255	SK-N-SH	brain:	n/a
46	chr7:102477205-102477255	HCPEpiC	choroid plexus:	n/a
47	chr7:102449340-102449390	HIPEpiC	eye:	n/a
48	chr7:102449340-102449390	SK-N-SH_RA	brain:	n/a
49	chr7:102500111-102500161	H1-hESC	embryonic stem cell:	embryo
50	chr7:102470281-102470331	HIPEpiC	eye:	n/a

(count:62 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:102462907..102465712-chr7:102475017..102477373,2	K562	blood:
2	chr7:102504642..102507106-chr7:102507263..102511653,3	K562	blood:
3	chr7:102501610..102503166-chr7:102508637..102510523,2	K562	blood:
4	chr7:102497049..102499033-chr7:102503041..102505939,2	K562	blood:
5	chr7:102446461..102450682-chr7:102452402..102456233,5	K562	blood:
6	chr7:102474929..102477472-chr7:102495351..102498066,2	K562	blood:
7	chr7:102513883..102516664-chr7:102520756..102522395,2	K562	blood:
8	chr7:102527046..102528879-chr7:102528977..102531238,2	MCF-7	breast:
9	chr7:102473443..102475589-chr7:102480022..102482918,2	K562	blood:
10	chr7:102522158..102525265-chr7:102531503..102535074,3	K562	blood:
11	chr7:102497060..102498758-chr7:102613043..102615053,2	K562	blood:
12	chr7:102474929..102477472-chr7:102495351..102498066,2	K562	blood:
13	chr7:102471265..102473661-chr7:102474795..102476825,2	K562	blood:
14	chr7:102466773..102468562-chr7:102472761..102475356,2	MCF-7	breast:
15	chr7:102470809..102472496-chr7:102473289..102475572,2	MCF-7	breast:
16	chr7:102513883..102516664-chr7:102520756..102522395,2	K562	blood:
17	chr7:102459925..102462268-chr7:102466191..102467871,2	K562	blood:
18	chr7:102501221..102503373-chr7:102515985..102518701,2	MCF-7	breast:
19	chr20:52596990..52599653-chr7:102503790..102506770,2	MCF-7	breast:
20	chr7:102526206..102528003-chr7:102535680..102538379,2	MCF-7	breast:
21	chr7:102489665..102492498-chr7:102495300..102497224,2	K562	blood:
22	chr7:102526206..102528003-chr7:102535680..102538379,2	MCF-7	breast:
23	chr7:102501610..102503166-chr7:102508637..102510523,2	K562	blood:
24	chr7:102516404..102517929-chr7:102714703..102716697,2	MCF-7	breast:
25	chr7:102452440..102454909-chr7:102615064..102617723,2	K562	blood:
26	chr7:102445308..102447740-chr7:102490751..102492572,2	K562	blood:
27	chr7:102501221..102503373-chr7:102515985..102518701,2	MCF-7	breast:
28	chr7:102535894..102537505-chr7:102552390..102554520,2	MCF-7	breast:
29	chr7:102458375..102460773-chr7:102462398..102464575,2	K562	blood:
30	chr7:102513072..102513724-chr9:129702545..129703389,2	MCF-7	breast:
31	chr7:102517307..102518855-chr7:102521320..102524235,2	MCF-7	breast:
32	chr7:102451931..102453738-chr7:102614138..102615717,2	K562	blood:
33	chr7:102489859..102491552-chr7:102503328..102506075,2	MCF-7	breast:
34	chr7:102459530..102461153-chr7:102484743..102487140,2	K562	blood:
35	chr7:102445308..102447740-chr7:102490751..102492572,2	K562	blood:
36	chr7:102483542..102485503-chr7:102492215..102494195,2	K562	blood:
37	chr7:102537736..102539276-chr7:102622119..102624837,2	MCF-7	breast:
38	chr7:102510827..102513027-chr7:102515036..102518141,3	K562	blood:
39	chr7:102499316..102501151-chr7:102502125..102504544,2	K562	blood:
40	chr7:102489859..102491552-chr7:102503328..102506075,2	MCF-7	breast:
41	chr7:102522158..102525265-chr7:102531503..102535074,3	K562	blood:
42	chr7:102446461..102450682-chr7:102452402..102456233,5	K562	blood:
43	chr7:102490998..102493774-chr7:102495300..102496979,2	K562	blood:
44	chr7:102473090..102475084-chr7:102477070..102479073,2	K562	blood:
45	chr7:102503409..102506375-chr7:102514987..102518844,3	K562	blood:
46	chr7:102517307..102518855-chr7:102521320..102524235,2	MCF-7	breast:
47	chr7:102517778..102519381-chr7:102714945..102717591,2	MCF-7	breast:
48	chr7:102490998..102493774-chr7:102495300..102496979,2	K562	blood:
49	chr7:102449182..102452214-chr7:102453198..102455672,3	K562	blood:
50	chr7:102449182..102452214-chr7:102453198..102455672,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC105052.1-2	chr7:102454781-102454863	NONHSAT122523
2	lnc-FAM185A-1	chr7:102497897-102498202	NONHSAT122525
3	lnc-AC105052.1-2	chr7:102453685-102453978	NONHSAT122523
4	lnc-AC105052.1-2	chr7:102456637-102456718	NONHSAT122523

No data

Variant related genes	Relation type
RNU6-1136P	TF binding region
FBXL13	TF binding region
RN7SKP198	TF binding region
RNU6-1136P	CpG island
FBXL13	CpG island
RN7SKP198	CpG island
ENSG00000238324	chromatin interactions
ENSG00000252643	chromatin interactions
ENSG00000230257	chromatin interactions
ENSG00000170632	chromatin interactions
ENSG00000161040	chromatin interactions
ENSG00000128606	chromatin interactions

Extended variants
information (count: 3310 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:3310 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10228495	chr7:102440184-102440185	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs538767931	chr7:102440185-102440186	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs183876884	chr7:102440197-102440198	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs144554208	chr7:102440249-102440250	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs187372487	chr7:102440257-102440258	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs554570080	chr7:102440328-102440329	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs530176693	chr7:102440343-102440344	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs576246948	chr7:102440356-102440357	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs543268328	chr7:102440364-102440365	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs558691925	chr7:102440405-102440406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs147821466	chr7:102440440-102440441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs545132044	chr7:102440448-102440449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs560203272	chr7:102440467-102440468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs193029188	chr7:102440508-102440509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs373775711	chr7:102440543-102440544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs542958851	chr7:102440566-102440567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs185717818	chr7:102440596-102440597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs531995597	chr7:102440656-102440657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs550126863	chr7:102440731-102440732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs190626753	chr7:102440738-102440739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs571845929	chr7:102440747-102440748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs2537388	chr7:102440754-102440755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs532746038	chr7:102440756-102440757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs547563764	chr7:102440796-102440797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs565735366	chr7:102440824-102440825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs6975388	chr7:102440844-102440845	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs554515748	chr7:102440865-102440866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs12113759	chr7:102440914-102440915	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs537381723	chr7:102440922-102440923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs558555659	chr7:102440975-102440976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs180986362	chr7:102440982-102440983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs75813832	chr7:102440990-102440991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs183729326	chr7:102440996-102440997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs370389193	chr7:102441029-102441030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs201498633	chr7:102441092-102441093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs566189095	chr7:102441099-102441100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs188159451	chr7:102441100-102441101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs113128984	chr7:102441133-102441134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs181354135	chr7:102441162-102441163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531593813	chr7:102441169-102441170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs6465873	chr7:102441180-102441181	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs570772823	chr7:102441194-102441195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs565576843	chr7:102441256-102441257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs80213030	chr7:102441259-102441260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs185530740	chr7:102441301-102441302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs547969927	chr7:102441348-102441349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs191631502	chr7:102441366-102441367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs181837990	chr7:102441370-102441371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs112048574	chr7:102441374-102441375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs187315928	chr7:102441533-102441534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
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
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
Prostate cancer	18632612	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	19907438	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD
abnormal development	18461090	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1324 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:102390800-102448800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr7:102391600-102448600	Weak transcription	Adipose Nuclei	Adipose
3	chr7:102416400-102467600	Weak transcription	Brain Anterior Caudate	brain
4	chr7:102419600-102454200	Weak transcription	Osteobl	bone
5	chr7:102419600-102456000	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr7:102419800-102454000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr7:102420400-102448600	Weak transcription	K562	blood
8	chr7:102420800-102449000	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr7:102421600-102449000	Weak transcription	Liver	Liver
10	chr7:102421600-102452000	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr7:102421600-102475600	Weak transcription	Fetal Thymus	thymus
12	chr7:102422000-102448800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr7:102422000-102474800	Weak transcription	Duodenum Mucosa	Duodenum
14	chr7:102422000-102476000	Weak transcription	Fetal Muscle Trunk	muscle
15	chr7:102436000-102454000	Weak transcription	NH-A	brain
16	chr7:102437200-102448800	Weak transcription	Fetal Stomach	stomach
17	chr7:102437400-102452000	Weak transcription	HUVEC	blood vessel
18	chr7:102437600-102449200	Weak transcription	Fetal Lung	lung
19	chr7:102439000-102459600	Weak transcription	Brain Hippocampus Middle	brain
20	chr7:102439600-102467400	Weak transcription	Thymus	Thymus
21	chr7:102439800-102463800	Weak transcription	Placenta Amnion	Placenta Amnion
22	chr7:102440000-102440200	Weak transcription	Primary T cells from cord blood	blood
23	chr7:102440000-102440400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr7:102440200-102440400	ZNF genes & repeats	Primary T cells from cord blood	blood
25	chr7:102440400-102449000	Weak transcription	Primary T cells from cord blood	blood
26	chr7:102443000-102451200	Weak transcription	Skeletal Muscle Male	skeletal muscle
27	chr7:102443800-102459600	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr7:102444400-102463200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr7:102445200-102451000	Weak transcription	Fetal Intestine Small	intestine
30	chr7:102445400-102445600	Active TSS	Fetal Brain Male	brain
31	chr7:102445600-102448800	Weak transcription	Rectal Mucosa Donor 31	rectum
32	chr7:102445600-102467600	Weak transcription	Stomach Smooth Muscle	stomach
33	chr7:102445600-102469200	Weak transcription	Fetal Brain Male	brain
34	chr7:102445800-102448800	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr7:102445800-102449000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr7:102445800-102449000	Weak transcription	Fetal Muscle Leg	muscle
37	chr7:102445800-102467400	Weak transcription	Lung	lung
38	chr7:102446200-102467400	Weak transcription	Primary T cells fromperipheralblood	blood
39	chr7:102446600-102448600	Weak transcription	Duodenum Smooth Muscle	Duodenum
40	chr7:102446800-102447400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr7:102446800-102447400	Enhancers	HepG2	liver
42	chr7:102447000-102448600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr7:102447000-102454000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr7:102447000-102454400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr7:102447000-102469400	Weak transcription	Brain Angular Gyrus	brain
46	chr7:102447200-102447400	Enhancers	Ovary	ovary
47	chr7:102447200-102453800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr7:102447200-102454000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr7:102447200-102467400	Weak transcription	Primary B cells from cord blood	blood
50	chr7:102447200-102469400	Weak transcription	Fetal Brain Female	brain

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