Variant report

Variant	esv3529902
Chromosome Location	chr18:6537233-6851509
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2365)
CpG islands
(count:427)
Chromatin interactive
region (count:82)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2365 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:6682253-6683739	K562	blood:	n/a	n/a
2	ARID3A	chr18:6686341-6686362	K562	blood:	n/a	n/a
3	ARID3A	chr18:6729971-6730743	K562	blood:	n/a	n/a
4	ARID3A	chr18:6728394-6729188	K562	blood:	n/a	n/a
5	ARID3A	chr18:6735402-6735545	K562	blood:	n/a	n/a
6	ARID3A	chr18:6543377-6543583	K562	blood:	n/a	n/a
7	ARID3A	chr18:6676089-6676517	K562	blood:	n/a	n/a
8	ARID3A	chr18:6684960-6685180	K562	blood:	n/a	n/a
9	ARID3A	chr18:6835362-6835608	HepG2	liver:	n/a	n/a
10	ARID3A	chr18:6741370-6741764	K562	blood:	n/a	n/a
11	ATF1	chr18:6640177-6640375	K562	blood:	n/a	n/a
12	ATF1	chr18:6676056-6676597	K562	blood:	n/a	n/a
13	ATF1	chr18:6836325-6836793	K562	blood:	n/a	n/a
14	ATF1	chr18:6741347-6741721	K562	blood:	n/a	n/a
15	ATF1	chr18:6767665-6767865	K562	blood:	n/a	n/a
16	ATF2	chr18:6613605-6614014	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr18:6613578-6613988	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr18:6752364-6752981	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr18:6752312-6752936	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF3	chr18:6836359-6836675	K562	blood:	n/a	n/a
21	ATF3	chr18:6729564-6730053	K562	blood:	n/a	chr18:6729600-6729609 chr18:6729723-6729732
22	ATF3	chr18:6741343-6741595	K562	blood:	n/a	n/a
23	BACH1	chr18:6729219-6730072	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr18:6706923-6706986	K562	blood:	n/a	n/a
25	BACH1	chr18:6741401-6741579	K562	blood:	n/a	chr18:6741513-6741527
26	BACH1	chr18:6682218-6683089	K562	blood:	n/a	n/a
27	BACH1	chr18:6676293-6676411	K562	blood:	n/a	n/a
28	BACH1	chr18:6543397-6543696	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr18:6741323-6741657	H1-hESC	embryonic stem cell:	n/a	chr18:6741513-6741527
30	BACH1	chr18:6746406-6746521	K562	blood:	n/a	n/a
31	BACH1	chr18:6682348-6682585	H1-hESC	embryonic stem cell:	n/a	n/a
32	BATF	chr18:6541281-6541620	GM12878	blood:	n/a	n/a
33	BCL11A	chr18:6752509-6752888	H1-hESC	embryonic stem cell:	n/a	n/a
34	BCL11A	chr18:6752560-6752887	H1-hESC	embryonic stem cell:	n/a	n/a
35	BCL3	chr18:6676221-6676460	K562	blood:	n/a	chr18:6676306-6676313
36	BHLHE40	chr18:6561639-6561762	K562	blood:	n/a	n/a
37	BHLHE40	chr18:6720407-6720429	K562	blood:	n/a	n/a
38	BHLHE40	chr18:6745702-6745827	K562	blood:	n/a	n/a
39	BHLHE40	chr18:6635346-6635562	K562	blood:	n/a	n/a
40	BHLHE40	chr18:6836478-6836689	K562	blood:	n/a	n/a
41	BHLHE40	chr18:6543498-6543694	K562	blood:	n/a	n/a
42	BHLHE40	chr18:6676130-6676745	K562	blood:	n/a	n/a
43	BHLHE40	chr18:6781274-6781391	K562	blood:	n/a	n/a
44	BHLHE40	chr18:6682620-6684172	K562	blood:	n/a	n/a
45	BHLHE40	chr18:6731529-6731530	K562	blood:	n/a	n/a
46	BHLHE40	chr18:6741221-6741268	K562	blood:	n/a	n/a
47	BHLHE40	chr18:6729199-6730217	K562	blood:	n/a	chr18:6729727-6729743
48	BRCA1	chr18:6591463-6591767	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr18:6661855-6662445	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr18:6659004-6659021	H1-hESC	embryonic stem cell:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:6725960-6726010	ECC-1	luminal epithelium:	n/a
2	chr18:6729810-6729860	GM12878	blood:	n/a
3	chr18:6834653-6834703	HCT-116	colon:	n/a
4	chr18:6725960-6726010	AG09319	gingival:	n/a
5	chr18:6834653-6834703	BJ	skin:	n/a
6	chr18:6834653-6834703	SKMC	muscle:	n/a
7	chr18:6733414-6733464	BE2_C	brain:	n/a
8	chr18:6835382-6835432	SK-N-SH_RA	brain:	n/a
9	chr18:6835382-6835432	AG09309	skin:	n/a
10	chr18:6730036-6730086	AG10803	skin:	n/a
11	chr18:6835382-6835432	BJ	skin:	n/a
12	chr18:6835382-6835432	HRPEpiC	eye:	n/a
13	chr18:6730036-6730086	HCT-116	colon:	n/a
14	chr18:6730036-6730086	HCPEpiC	choroid plexus:	n/a
15	chr18:6725960-6726010	SK-N-SH_RA	brain:	n/a
16	chr18:6729810-6729860	NH-A	brain:	n/a
17	chr18:6730036-6730086	HCF	heart:	n/a
18	chr18:6730036-6730086	Jurkat	blood:	n/a
19	chr18:6833417-6833467	HUVEC	blood vessel:	n/a
20	chr18:6835382-6835432	LNCaP	prostate:	n/a
21	chr18:6833417-6833467	H1-hESC	embryonic stem cell:	embryo
22	chr18:6733414-6733464	T-47D	breast:	n/a
23	chr18:6835382-6835432	Jurkat	blood:	n/a
24	chr18:6834653-6834703	Hela-S3	cervix:	n/a
25	chr18:6729810-6729860	K562	blood:	n/a
26	chr18:6729810-6729860	BE2_C	brain:	n/a
27	chr18:6733414-6733464	ECC-1	luminal epithelium:	n/a
28	chr18:6730036-6730086	NHDF-neo	bronchial:	n/a
29	chr18:6729810-6729860	HL-60	blood:	n/a
30	chr18:6730036-6730086	NHBE	bronchial:	n/a
31	chr18:6834653-6834703	NH-A	brain:	n/a
32	chr18:6729810-6729860	RPTEC	kidney:	n/a
33	chr18:6729810-6729860	MCF-7	breast:	n/a
34	chr18:6729810-6729860	IMR90	lung:	fetal
35	chr18:6833417-6833467	HMEC	breast:	n/a
36	chr18:6733414-6733464	HCM	heart:	n/a
37	chr18:6729810-6729860	NT2-D1	testis:	n/a
38	chr18:6833417-6833467	GM12878	blood:	n/a
39	chr18:6729810-6729860	SKMC	muscle:	n/a
40	chr18:6835382-6835432	HepG2	liver:	n/a
41	chr18:6733414-6733464	Caco-2	colon:	n/a
42	chr18:6729810-6729860	BJ	skin:	n/a
43	chr18:6833417-6833467	HNPCEpiC	eye:	n/a
44	chr18:6835382-6835432	T-47D	breast:	n/a
45	chr18:6833417-6833467	ECC-1	luminal epithelium:	n/a
46	chr18:6834653-6834703	ProgFib	skin:	n/a
47	chr18:6834653-6834703	HCF	heart:	n/a
48	chr18:6725960-6726010	NHDF-neo	bronchial:	n/a
49	chr18:6834653-6834703	BE2_C	brain:	n/a
50	chr18:6835382-6835432	HIPEpiC	eye:	n/a

(count:82 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr18:6543479..6544036-chr18:6732819..6733527,2	MCF-7	breast:
2	chr18:6543387..6543995-chr18:7022410..7022919,2	MCF-7	breast:
3	chr18:6721256..6723757-chr18:6727643..6729991,2	K562	blood:
4	chr18:6742579..6744550-chr18:6848151..6850631,2	K562	blood:
5	chr18:6717313..6721364-chr18:6721501..6725687,5	K562	blood:
6	chr18:6679662..6682250-chr18:6685421..6688105,2	K562	blood:
7	chr18:6780742..6782495-chr18:6812998..6814877,2	K562	blood:
8	chr18:6708117..6710489-chr18:6714174..6717600,3	K562	blood:
9	chr18:6667604..6670342-chr18:6728506..6731049,3	K562	blood:
10	chr18:6592401..6595122-chr18:6603404..6606358,2	K562	blood:
11	chr18:5867118..5868077-chr18:6541162..6541809,2	MCF-7	breast:
12	chr18:6725447..6727785-chr18:6730502..6732481,2	K562	blood:
13	chr18:6770718..6772411-chr18:6775406..6777040,2	K562	blood:
14	chr18:6743142..6745780-chr18:6746474..6749078,2	K562	blood:
15	chr18:6593291..6595462-chr18:6599669..6601828,3	K562	blood:
16	chr18:6728466..6731332-chr18:6734924..6737475,3	K562	blood:
17	chr18:6774418..6777121-chr18:6778867..6780736,2	K562	blood:
18	chr18:6579661..6581672-chr18:6583451..6585136,2	K562	blood:
19	chr18:6623674..6626604-chr18:6633979..6636538,2	MCF-7	breast:
20	chr18:5073001..5073821-chr18:6541209..6541754,2	MCF-7	breast:
21	chr18:6743142..6744914-chr18:6746474..6748281,2	K562	blood:
22	chr18:6543479..6544036-chr18:6732819..6733527,2	MCF-7	breast:
23	chr18:6725183..6727933-chr18:6730767..6732565,3	K562	blood:
24	chr18:6675021..6678656-chr18:6685638..6689363,5	K562	blood:
25	chr18:6685911..6687499-chr18:6763330..6765130,2	K562	blood:
26	chr18:6731530..6734164-chr18:6740298..6742070,2	K562	blood:
27	chr18:6711773..6713499-chr18:6727376..6728976,2	K562	blood:
28	chr16:2202863..2205722-chr18:6634230..6636566,2	K562	blood:
29	chr18:6685044..6687268-chr18:6731388..6733678,2	K562	blood:
30	chr18:6711773..6713499-chr18:6727376..6728976,2	K562	blood:
31	chr18:6676534..6678660-chr18:6681129..6684037,2	K562	blood:
32	chr18:6542623..6543373-chr18:6885965..6886489,2	K562	blood:
33	chr18:6677160..6680271-chr18:6681129..6683150,5	K562	blood:
34	chr18:6715232..6717469-chr18:6730082..6731975,2	K562	blood:
35	chr18:6689018..6691882-chr18:6694306..6696687,2	K562	blood:
36	chr18:6774418..6777121-chr18:6778867..6780736,2	K562	blood:
37	chr18:6675021..6678656-chr18:6685638..6689363,5	K562	blood:
38	chr18:6683311..6686830-chr18:6687700..6692231,7	K562	blood:
39	chr18:6551949..6554586-chr18:6555570..6558169,2	MCF-7	breast:
40	chr18:6708117..6710489-chr18:6714174..6717600,3	K562	blood:
41	chr18:5867908..5868506-chr18:6541176..6541747,2	MCF-7	breast:
42	chr18:6834903..6836491-chr18:6842166..6845111,2	K562	blood:
43	chr18:6579661..6581672-chr18:6583451..6585136,2	K562	blood:
44	chr18:6672907..6676743-chr18:6676985..6680326,4	K562	blood:
45	chr18:5296491..5298171-chr18:6658883..6660458,2	MCF-7	breast:
46	chr18:5879246..5879912-chr18:6540886..6542138,3	MCF-7	breast:
47	chr18:6743142..6745780-chr18:6746474..6749078,2	K562	blood:
48	chr18:6742579..6744550-chr18:6848151..6850631,2	K562	blood:
49	chr18:6715232..6717469-chr18:6730082..6731975,2	K562	blood:
50	chr18:6717313..6721364-chr18:6721501..6725687,5	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LAMA1-3	chr18:6728833-6729167	XLOC_012748
2	lnc-ARHGAP28-8	chr18:6601539-6601834	NONHSAT057115
3	lnc-LAMA1-3	chr18:6728820-6729167	ENSG00000266441.1
4	lnc-ARHGAP28-6	chr18:6727002-6728980	NONHSAT057118
5	lnc-LAMA1-3	chr18:6729719-6729916	XLOC_012748
6	lnc-ARHGAP28-2	chr18:6557821-6558401	ENSG00000265174.1
7	lnc-LAMA1-3	chr18:6729719-6729861	ENSG00000266441.1
8	lnc-L3MBTL4-1	chr18:6641970-6642477	ENSG00000261627.1
9	lnc-ARHGAP28-2	chr18:6558577-6558653	ENSG00000265174.1
10	lnc-LRRC30-3	chr18:6774030-6774233	XLOC_012619
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
ENSG00000260260	chromatin interactions
ENSG00000167964	chromatin interactions
ENSG00000243591	chromatin interactions
ENSG00000206630	chromatin interactions
ENSG00000131653	chromatin interactions
ENSG00000265174	chromatin interactions
ENSG00000088756	chromatin interactions
ENSG00000266441	chromatin interactions
ENSG00000198081	chromatin interactions

Extended variants
information (count: 11802 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:11802 , 50 per page) page: 1 2 3 4 5 6 7 ... 237

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536871908	chr18:6537376-6537377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs556719229	chr18:6537383-6537384	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs576168522	chr18:6537427-6537428	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs542306240	chr18:6537446-6537447	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs555529723	chr18:6537463-6537464	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs149296703	chr18:6537469-6537470	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs369813607	chr18:6537506-6537507	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs541040039	chr18:6537520-6537521	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs564799623	chr18:6537522-6537523	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs374214177	chr18:6537537-6537538	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs186930575	chr18:6537587-6537588	Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs114135380	chr18:6537646-6537647	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs529421624	chr18:6537651-6537652	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs549073983	chr18:6537658-6537659	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs572541619	chr18:6537667-6537668	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs559147440	chr18:6537679-6537680	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs541502692	chr18:6537722-6537723	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs528109254	chr18:6537844-6537845	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs550937200	chr18:6538004-6538005	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs370780832	chr18:6538005-6538006	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs564961980	chr18:6538010-6538011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs571238919	chr18:6538064-6538065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs536938637	chr18:6538067-6538068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs190540616	chr18:6538078-6538079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs58262376	chr18:6538098-6538099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs536017685	chr18:6538168-6538169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs555852193	chr18:6538230-6538231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs573078277	chr18:6538255-6538256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs372982524	chr18:6538277-6538278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs377172572	chr18:6538296-6538297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs139392435	chr18:6538415-6538416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs533996945	chr18:6538419-6538420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs370233162	chr18:6538434-6538435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs182378854	chr18:6538440-6538441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs578262268	chr18:6538478-6538479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs544133434	chr18:6538482-6538483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs187094822	chr18:6538495-6538496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs563933366	chr18:6538499-6538500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs189574106	chr18:6538526-6538527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542822702	chr18:6538554-6538555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs373685827	chr18:6538623-6538624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs559424590	chr18:6538628-6538629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs570538250	chr18:6538665-6538666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs528156588	chr18:6538707-6538708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs551000462	chr18:6538710-6538711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs564535055	chr18:6538742-6538743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs530379453	chr18:6538777-6538778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs182145319	chr18:6538788-6538789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs72634397	chr18:6538849-6538850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs536475958	chr18:6538936-6538937	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:3163 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:6536800-6537400	Enhancers	Ovary	ovary
2	chr18:6536800-6538000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr18:6537000-6537400	Enhancers	Fetal Lung	lung
4	chr18:6537200-6537400	Enhancers	Adipose Nuclei	Adipose
5	chr18:6537200-6537600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr18:6537400-6537600	Flanking Active TSS	Fetal Lung	lung
7	chr18:6537400-6537800	Active TSS	Adipose Nuclei	Adipose
8	chr18:6537400-6538000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr18:6537400-6538200	Enhancers	Liver	Liver
10	chr18:6537600-6538000	Active TSS	Fetal Lung	lung
11	chr18:6537800-6538200	Enhancers	Adipose Nuclei	Adipose
12	chr18:6538000-6540000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr18:6538000-6540200	Weak transcription	Fetal Lung	lung
14	chr18:6538200-6546000	Weak transcription	Adipose Nuclei	Adipose
15	chr18:6539200-6540200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr18:6540000-6540800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr18:6540000-6540800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr18:6540000-6541400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr18:6540000-6541400	Enhancers	Hela-S3	cervix
20	chr18:6540000-6542000	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr18:6540000-6542000	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr18:6540200-6541200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr18:6540200-6541200	Enhancers	Fetal Lung	lung
24	chr18:6540400-6541000	Enhancers	HMEC	breast
25	chr18:6540400-6541200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr18:6540400-6541800	Enhancers	HUVEC	blood vessel
27	chr18:6540600-6541200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr18:6540800-6541000	Enhancers	Brain Germinal Matrix	brain
29	chr18:6540800-6541200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr18:6540800-6545800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr18:6541000-6541800	Weak transcription	Brain Germinal Matrix	brain
32	chr18:6541000-6546000	Weak transcription	HMEC	breast
33	chr18:6541200-6541800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr18:6541200-6542800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr18:6541200-6543600	Weak transcription	Fetal Lung	lung
36	chr18:6541400-6545600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr18:6541800-6544000	Enhancers	Brain Germinal Matrix	brain
38	chr18:6542000-6543400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr18:6542000-6547600	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr18:6542400-6543200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr18:6542800-6547600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr18:6543000-6543800	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr18:6543400-6546200	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr18:6543600-6543800	Enhancers	HSMMtube	muscle
45	chr18:6543600-6544000	Enhancers	Fetal Brain Female	brain
46	chr18:6543600-6544600	Enhancers	Ovary	ovary
47	chr18:6543600-6544800	Enhancers	Fetal Lung	lung
48	chr18:6543800-6544000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr18:6544600-6545400	Weak transcription	Ovary	ovary
50	chr18:6545400-6545600	Enhancers	Ovary	ovary

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