Variant report

Variant	nsv543629
Chromosome Location	chr18:6527292-6790869
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2241)
CpG islands
(count:245)
Chromatin interactive
region (count:78)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2241 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:6543377-6543583	K562	blood:	n/a	n/a
2	ARID3A	chr18:6729971-6730743	K562	blood:	n/a	n/a
3	ARID3A	chr18:6682253-6683739	K562	blood:	n/a	n/a
4	ARID3A	chr18:6741370-6741764	K562	blood:	n/a	n/a
5	ARID3A	chr18:6728394-6729188	K562	blood:	n/a	n/a
6	ARID3A	chr18:6735402-6735545	K562	blood:	n/a	n/a
7	ARID3A	chr18:6684960-6685180	K562	blood:	n/a	n/a
8	ARID3A	chr18:6686341-6686362	K562	blood:	n/a	n/a
9	ARID3A	chr18:6676089-6676517	K562	blood:	n/a	n/a
10	ATF1	chr18:6640177-6640375	K562	blood:	n/a	n/a
11	ATF1	chr18:6767665-6767865	K562	blood:	n/a	n/a
12	ATF1	chr18:6741347-6741721	K562	blood:	n/a	n/a
13	ATF1	chr18:6676056-6676597	K562	blood:	n/a	n/a
14	ATF2	chr18:6752312-6752936	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr18:6613578-6613988	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr18:6752364-6752981	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr18:6613605-6614014	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF3	chr18:6741343-6741595	K562	blood:	n/a	n/a
19	ATF3	chr18:6729564-6730053	K562	blood:	n/a	chr18:6729600-6729609 chr18:6729723-6729732
20	BACH1	chr18:6741323-6741657	H1-hESC	embryonic stem cell:	n/a	chr18:6741513-6741527
21	BACH1	chr18:6682218-6683089	K562	blood:	n/a	n/a
22	BACH1	chr18:6543397-6543696	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr18:6729219-6730072	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr18:6676293-6676411	K562	blood:	n/a	n/a
25	BACH1	chr18:6741401-6741579	K562	blood:	n/a	chr18:6741513-6741527
26	BACH1	chr18:6682348-6682585	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr18:6706923-6706986	K562	blood:	n/a	n/a
28	BACH1	chr18:6746406-6746521	K562	blood:	n/a	n/a
29	BATF	chr18:6541281-6541620	GM12878	blood:	n/a	n/a
30	BCL11A	chr18:6752560-6752887	H1-hESC	embryonic stem cell:	n/a	n/a
31	BCL11A	chr18:6752509-6752888	H1-hESC	embryonic stem cell:	n/a	n/a
32	BCL3	chr18:6676221-6676460	K562	blood:	n/a	chr18:6676306-6676313
33	BHLHE40	chr18:6729199-6730217	K562	blood:	n/a	chr18:6729727-6729743
34	BHLHE40	chr18:6781274-6781391	K562	blood:	n/a	n/a
35	BHLHE40	chr18:6682620-6684172	K562	blood:	n/a	n/a
36	BHLHE40	chr18:6543498-6543694	K562	blood:	n/a	n/a
37	BHLHE40	chr18:6676130-6676745	K562	blood:	n/a	n/a
38	BHLHE40	chr18:6741221-6741268	K562	blood:	n/a	n/a
39	BHLHE40	chr18:6720407-6720429	K562	blood:	n/a	n/a
40	BHLHE40	chr18:6561639-6561762	K562	blood:	n/a	n/a
41	BHLHE40	chr18:6635346-6635562	K562	blood:	n/a	n/a
42	BHLHE40	chr18:6745702-6745827	K562	blood:	n/a	n/a
43	BHLHE40	chr18:6731529-6731530	K562	blood:	n/a	n/a
44	BRCA1	chr18:6726685-6726880	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr18:6574905-6575003	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr18:6719353-6720156	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr18:6659004-6659021	H1-hESC	embryonic stem cell:	n/a	n/a
48	BRCA1	chr18:6729660-6730193	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr18:6566046-6566910	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr18:6661855-6662445	Hela-S3	cervix:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:6725960-6726010	GM12891	blood:	n/a
2	chr18:6725960-6726010	GM12891	blood:	n/a
3	chr18:6730036-6730086	NHDF-neo	bronchial:	n/a
4	chr18:6725960-6726010	Jurkat	blood:	n/a
5	chr18:6733414-6733464	HCM	heart:	n/a
6	chr18:6730036-6730086	MCF10A-Er-Src	breast:	n/a
7	chr18:6729810-6729860	Jurkat	blood:	n/a
8	chr18:6725960-6726010	ECC-1	luminal epithelium:	n/a
9	chr18:6730036-6730086	NHBE	bronchial:	n/a
10	chr18:6733414-6733464	HRE	kidney:	n/a
11	chr18:6733414-6733464	HAEpiC	amniotic membrane:	n/a
12	chr18:6730036-6730086	GM06990	blood:	n/a
13	chr18:6725960-6726010	Hepatocyte	liver:	n/a
14	chr18:6730036-6730086	A549	lung:	n/a
15	chr18:6725960-6726010	HRCEpiC	kidney:	n/a
16	chr18:6725960-6726010	HEEpiC	esophagus:	n/a
17	chr18:6730036-6730086	HRE	kidney:	n/a
18	chr18:6730036-6730086	SKMC	muscle:	n/a
19	chr18:6725960-6726010	SAEC	small airway:	n/a
20	chr18:6730036-6730086	HPAEpiC	pulmonary alveolar:	n/a
21	chr18:6729810-6729860	AoSMC	blood vessel:	n/a
22	chr18:6725960-6726010	SK-N-MC	brain:	n/a
23	chr18:6733414-6733464	A549	lung:	n/a
24	chr18:6729810-6729860	ProgFib	skin:	n/a
25	chr18:6733414-6733464	LNCaP	prostate:	n/a
26	chr18:6729810-6729860	SK-N-MC	brain:	n/a
27	chr18:6733414-6733464	HMEC	breast:	n/a
28	chr18:6730036-6730086	U87	brain:	n/a
29	chr18:6729810-6729860	MCF10A-Er-Src	breast:	n/a
30	chr18:6733414-6733464	ovcar-3	ovarian:	n/a
31	chr18:6733414-6733464	HL-60	blood:	n/a
32	chr18:6730036-6730086	PrEC	prostate:	n/a
33	chr18:6733414-6733464	MCF10A-Er-Src	breast:	n/a
34	chr18:6725960-6726010	HCT-116	colon:	n/a
35	chr18:6733414-6733464	NHDF-neo	bronchial:	n/a
36	chr18:6729810-6729860	LNCaP	prostate:	n/a
37	chr18:6733414-6733464	BE2_C	brain:	n/a
38	chr18:6725960-6726010	AG10803	skin:	n/a
39	chr18:6733414-6733464	GM12892	blood:	n/a
40	chr18:6725960-6726010	GM12892	blood:	n/a
41	chr18:6733414-6733464	GM12891	blood:	n/a
42	chr18:6725960-6726010	CMK	blood:	n/a
43	chr18:6729810-6729860	HCM	heart:	n/a
44	chr18:6729810-6729860	HRPEpiC	eye:	n/a
45	chr18:6729810-6729860	NB4	blood:	n/a
46	chr18:6729810-6729860	HIPEpiC	eye:	n/a
47	chr18:6730036-6730086	HepG2	liver:	n/a
48	chr18:6730036-6730086	PFSK-1	brain:	n/a
49	chr18:6729810-6729860	AG04449	skin:	fetal
50	chr18:6733414-6733464	AG04449	skin:	fetal

(count:78 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr18:6725447..6727785-chr18:6730502..6732481,2	K562	blood:
2	chr18:5293641..5295878-chr18:6683464..6685082,2	K562	blood:
3	chr18:6543609..6544152-chr18:6886204..6886860,2	MCF-7	breast:
4	chr18:6593291..6595462-chr18:6599669..6601828,3	K562	blood:
5	chr18:6725447..6727785-chr18:6730502..6732481,2	K562	blood:
6	chr18:6677160..6680271-chr18:6681129..6683150,5	K562	blood:
7	chr18:6728466..6731332-chr18:6734924..6737475,3	K562	blood:
8	chr18:6715232..6717469-chr18:6730082..6731975,2	K562	blood:
9	chr18:6599305..6601149-chr18:6602412..6604670,2	K562	blood:
10	chr18:6681278..6684009-chr18:6728547..6731673,3	K562	blood:
11	chr18:6682078..6684757-chr18:6693347..6696063,3	K562	blood:
12	chr18:6728427..6731756-chr18:6733180..6736638,5	K562	blood:
13	chr18:6743142..6745780-chr18:6746474..6749078,2	K562	blood:
14	chr18:6717313..6721364-chr18:6721501..6725687,5	K562	blood:
15	chr18:6715232..6717469-chr18:6730082..6731975,2	K562	blood:
16	chr18:6780742..6782495-chr18:6812998..6814877,2	K562	blood:
17	chr18:6717313..6721364-chr18:6721501..6725687,5	K562	blood:
18	chr18:6774418..6777121-chr18:6778867..6780736,2	K562	blood:
19	chr18:6713759..6716499-chr18:6718333..6720932,2	MCF-7	breast:
20	chr18:6774418..6777121-chr18:6778867..6780736,2	K562	blood:
21	chr18:6689018..6691882-chr18:6694306..6696687,2	K562	blood:
22	chr18:6675021..6678656-chr18:6685638..6689363,5	K562	blood:
23	chr18:6668807..6670377-chr18:6672389..6675237,2	K562	blood:
24	chr18:6689018..6691882-chr18:6694306..6696687,2	K562	blood:
25	chr18:6743142..6744914-chr18:6746474..6748281,2	K562	blood:
26	chr18:6543450..6543991-chr18:6885879..6886587,3	K562	blood:
27	chr18:6725183..6727933-chr18:6730767..6732565,3	K562	blood:
28	chr18:6542623..6543373-chr18:6885965..6886489,2	K562	blood:
29	chr18:6676534..6678660-chr18:6681129..6684037,2	K562	blood:
30	chr18:6683030..6685856-chr18:6737464..6739886,2	K562	blood:
31	chr18:6683311..6686830-chr18:6687700..6692231,7	K562	blood:
32	chr18:6713759..6716499-chr18:6718333..6720932,2	MCF-7	breast:
33	chr18:6676534..6678660-chr18:6681129..6684037,2	K562	blood:
34	chr18:6599305..6601149-chr18:6602412..6604670,2	K562	blood:
35	chr18:6668807..6670377-chr18:6672389..6675237,2	K562	blood:
36	chr18:5879246..5879912-chr18:6540886..6542138,3	MCF-7	breast:
37	chr18:6543387..6543995-chr18:7022410..7022919,2	MCF-7	breast:
38	chr18:6725183..6727933-chr18:6730767..6732565,3	K562	blood:
39	chr18:6711773..6713499-chr18:6727376..6728976,2	K562	blood:
40	chr18:6711773..6713499-chr18:6727376..6728976,2	K562	blood:
41	chr18:6731530..6734164-chr18:6740298..6742070,2	K562	blood:
42	chr18:5867118..5868077-chr18:6541162..6541809,2	MCF-7	breast:
43	chr18:6708117..6710489-chr18:6714174..6717600,3	K562	blood:
44	chr18:6770718..6772411-chr18:6775406..6777040,2	K562	blood:
45	chr18:6743142..6745780-chr18:6746474..6749078,2	K562	blood:
46	chr18:6685044..6687268-chr18:6731388..6733678,2	K562	blood:
47	chr18:6721256..6723757-chr18:6727643..6729991,2	K562	blood:
48	chr18:6682078..6684757-chr18:6693347..6696063,3	K562	blood:
49	chr18:6543479..6544036-chr18:6732819..6733527,2	MCF-7	breast:
50	chr18:6623674..6626604-chr18:6633979..6636538,2	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LAMA1-3	chr18:6728820-6729167	ENSG00000266441.1
2	lnc-LAMA1-3	chr18:6729719-6729916	XLOC_012748
3	lnc-LRRC30-3	chr18:6774030-6774233	XLOC_012619
4	lnc-LAMA1-3	chr18:6729719-6729861	ENSG00000266441.1
5	lnc-ARHGAP28-2	chr18:6558577-6558653	ENSG00000265174.1
6	lnc-ARHGAP28-6	chr18:6727002-6728980	NONHSAT057118
7	lnc-L3MBTL4-1	chr18:6641970-6642477	ENSG00000261627.1
8	lnc-ARHGAP28-8	chr18:6601539-6601834	NONHSAT057115
9	lnc-ARHGAP28-2	chr18:6557821-6558401	ENSG00000265174.1
10	lnc-LAMA1-3	chr18:6728833-6729167	XLOC_012748
11	lnc-LRRC30-3	chr18:6778921-6779022	XLOC_012619

No data

Variant related genes	Relation type
RN7SL282P	TF binding region
ARHGAP28	TF binding region
ENSG00000265174	TF binding region
ENSG00000266441	TF binding region
ENSG00000261627	TF binding region
RN7SL282P	CpG island
ARHGAP28	CpG island
ENSG00000265174	CpG island
ENSG00000266441	CpG island
ENSG00000261627	CpG island
ENSG00000131653	chromatin interactions
ENSG00000167964	chromatin interactions
ENSG00000088756	chromatin interactions
ENSG00000243591	chromatin interactions
ENSG00000266441	chromatin interactions
ENSG00000198081	chromatin interactions
ENSG00000265174	chromatin interactions
ENSG00000206630	chromatin interactions
ENSG00000260260	chromatin interactions

Extended variants
information (count: 9582 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:9582 , 50 per page) page: 1 2 3 4 5 6 7 ... 192

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144197142	chr18:6535302-6535303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs146557998	chr18:6535339-6535340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs538142227	chr18:6535425-6535426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs141287163	chr18:6535465-6535466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs568562941	chr18:6535467-6535468	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs534359937	chr18:6535493-6535494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs73940937	chr18:6535515-6535516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs143667180	chr18:6535529-6535530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs539467482	chr18:6535537-6535538	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs35739822	chr18:6535616-6535617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs181215295	chr18:6535659-6535660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs12457089	chr18:6535671-6535672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs576444751	chr18:6535687-6535688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs542140469	chr18:6535689-6535690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs184201419	chr18:6535699-6535700	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs572164428	chr18:6535711-6535712	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs541192781	chr18:6535712-6535713	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs543677417	chr18:6535718-6535719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs35136036	chr18:6535729-6535730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs560413454	chr18:6535736-6535737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs145769857	chr18:6535809-6535810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs148971317	chr18:6535831-6535832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs11875727	chr18:6535878-6535879	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs7407217	chr18:6535904-6535905	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs188095080	chr18:6535981-6535982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs558928330	chr18:6536007-6536008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs534148639	chr18:6536017-6536018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs117204258	chr18:6536047-6536048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs570487858	chr18:6536048-6536049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs539529266	chr18:6536076-6536077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs75437224	chr18:6536096-6536097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs7407438	chr18:6536103-6536104	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs535409194	chr18:6536128-6536129	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs555396661	chr18:6536163-6536164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs112563961	chr18:6536170-6536171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs74380423	chr18:6536177-6536178	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs544360643	chr18:6536192-6536193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs148166707	chr18:6536197-6536198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs115413034	chr18:6536255-6536256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs62081396	chr18:6536267-6536268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs576972253	chr18:6536289-6536290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs142665466	chr18:6536304-6536305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs180934183	chr18:6536318-6536319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs561131215	chr18:6536324-6536325	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs186098356	chr18:6536326-6536327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs114480885	chr18:6536327-6536328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs527970265	chr18:6536337-6536338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs375872484	chr18:6536367-6536368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs530260390	chr18:6536402-6536403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs547714857	chr18:6536412-6536413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
head and neck squamous cell carcinoma	17671120	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Renal cell carcinoma	18765545	CNVD
Heart disease	21282601	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Acute myeloid leukemia	16864856	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Kartagener syndrome	16639409	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Cancer	21183584	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Human rectal carcinomas	16397240	CNVD
Colorectal cancer	16272173	CNVD
Colorectal cancer	19150955	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Autism	20808228	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Retinoblastoma	21504564	CNVD
Breast cancer	17133270	CNVD
Glioblastoma multiforme	21922591	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Obesity	20622171	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2808 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:6535200-6536400	Enhancers	Ovary	ovary
2	chr18:6535800-6536000	Enhancers	Fetal Lung	lung
3	chr18:6536000-6537000	Weak transcription	Fetal Lung	lung
4	chr18:6536400-6536800	Weak transcription	Ovary	ovary
5	chr18:6536800-6537400	Enhancers	Ovary	ovary
6	chr18:6536800-6538000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr18:6537000-6537400	Enhancers	Fetal Lung	lung
8	chr18:6537200-6537400	Enhancers	Adipose Nuclei	Adipose
9	chr18:6537200-6537600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr18:6537400-6537600	Flanking Active TSS	Fetal Lung	lung
11	chr18:6537400-6537800	Active TSS	Adipose Nuclei	Adipose
12	chr18:6537400-6538000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr18:6537400-6538200	Enhancers	Liver	Liver
14	chr18:6537600-6538000	Active TSS	Fetal Lung	lung
15	chr18:6537800-6538200	Enhancers	Adipose Nuclei	Adipose
16	chr18:6538000-6540000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr18:6538000-6540200	Weak transcription	Fetal Lung	lung
18	chr18:6538200-6546000	Weak transcription	Adipose Nuclei	Adipose
19	chr18:6539200-6540200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr18:6540000-6540800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr18:6540000-6540800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr18:6540000-6541400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr18:6540000-6541400	Enhancers	Hela-S3	cervix
24	chr18:6540000-6542000	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr18:6540000-6542000	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr18:6540200-6541200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr18:6540200-6541200	Enhancers	Fetal Lung	lung
28	chr18:6540400-6541000	Enhancers	HMEC	breast
29	chr18:6540400-6541200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr18:6540400-6541800	Enhancers	HUVEC	blood vessel
31	chr18:6540600-6541200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr18:6540800-6541000	Enhancers	Brain Germinal Matrix	brain
33	chr18:6540800-6541200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr18:6540800-6545800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr18:6541000-6541800	Weak transcription	Brain Germinal Matrix	brain
36	chr18:6541000-6546000	Weak transcription	HMEC	breast
37	chr18:6541200-6541800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr18:6541200-6542800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr18:6541200-6543600	Weak transcription	Fetal Lung	lung
40	chr18:6541400-6545600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr18:6541800-6544000	Enhancers	Brain Germinal Matrix	brain
42	chr18:6542000-6543400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr18:6542000-6547600	Weak transcription	HUES64 Cell Line	embryonic stem cell
44	chr18:6542400-6543200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr18:6542800-6547600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr18:6543000-6543800	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr18:6543400-6546200	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr18:6543600-6543800	Enhancers	HSMMtube	muscle
49	chr18:6543600-6544000	Enhancers	Fetal Brain Female	brain
50	chr18:6543600-6544600	Enhancers	Ovary	ovary

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