Variant report

Variant	esv2752406
Chromosome Location	chr11:59490424-59529524
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:987)
CpG islands
(count:732)
Chromatin interactive
region (count:49)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:987 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:59523254-59523785	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:59521549-59521749	K562	blood:	n/a	n/a
3	ARID3A	chr11:59523419-59523921	K562	blood:	n/a	n/a
4	ARID3A	chr11:59524418-59524618	K562	blood:	n/a	n/a
5	ATF2	chr11:59521422-59521868	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr11:59521445-59521896	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr11:59521454-59521976	GM12878	blood:	n/a	n/a
8	ATF3	chr11:59523170-59523502	K562	blood:	n/a	n/a
9	ATF3	chr11:59521495-59521831	K562	blood:	n/a	n/a
10	ATF3	chr11:59523431-59523657	K562	blood:	n/a	n/a
11	ATF3	chr11:59523117-59523395	K562	blood:	n/a	n/a
12	BACH1	chr11:59522316-59522839	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr11:59521481-59521838	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr11:59524392-59524707	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr11:59524098-59524690	K562	blood:	n/a	n/a
16	BATF	chr11:59524405-59524623	GM12878	blood:	n/a	chr11:59524540-59524551
17	BATF	chr11:59524441-59524676	GM12878	blood:	n/a	chr11:59524540-59524551
18	BHLHE40	chr11:59523092-59523651	HepG2	liver:	n/a	n/a
19	BHLHE40	chr11:59516559-59516677	K562	blood:	n/a	n/a
20	BHLHE40	chr11:59523246-59523639	A549	lung:	n/a	n/a
21	BHLHE40	chr11:59521493-59521818	GM12878	blood:	n/a	n/a
22	BHLHE40	chr11:59521511-59523765	K562	blood:	n/a	chr11:59522833-59522849
23	BHLHE40	chr11:59524324-59524737	K562	blood:	n/a	n/a
24	BRCA1	chr11:59523192-59523757	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr11:59521602-59521603	GM12878	blood:	n/a	n/a
26	BRCA1	chr11:59522313-59522619	Hela-S3	cervix:	n/a	n/a
27	CBX3	chr11:59523076-59523821	K562	blood:	n/a	n/a
28	CBX3	chr11:59521461-59521771	K562	blood:	n/a	n/a
29	CBX3	chr11:59521296-59522730	K562	blood:	n/a	n/a
30	CCNT2	chr11:59522529-59523681	K562	blood:	n/a	chr11:59523266-59523275 chr11:59523261-59523270 chr11:59523641-59523650
31	CCNT2	chr11:59521553-59521847	K562	blood:	n/a	n/a
32	CEBPB	chr11:59497392-59497738	IMR90	lung:	n/a	chr11:59497563-59497574
33	CEBPB	chr11:59521371-59521843	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr11:59497382-59497705	K562	blood:	n/a	chr11:59497563-59497574
35	CEBPB	chr11:59497493-59497612	H1-hESC	embryonic stem cell:	n/a	chr11:59497563-59497574
36	CEBPB	chr11:59497389-59497735	HepG2	liver:	n/a	chr11:59497563-59497574
37	CEBPB	chr11:59502973-59502977	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr11:59521436-59521605	K562	blood:	n/a	n/a
39	CEBPB	chr11:59521401-59521635	HepG2	liver:	n/a	n/a
40	CEBPB	chr11:59515550-59515822	K562	blood:	n/a	n/a
41	CEBPB	chr11:59498614-59498893	HepG2	liver:	n/a	n/a
42	CEBPB	chr11:59521443-59521800	K562	blood:	n/a	n/a
43	CEBPB	chr11:59522250-59522570	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr11:59523142-59523842	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr11:59497385-59497708	A549	lung:	n/a	chr11:59497563-59497574
46	CEBPB	chr11:59521431-59521818	Hela-S3	cervix:	n/a	n/a
47	CEBPD	chr11:59523059-59523726	K562	blood:	n/a	n/a
48	CHD1	chr11:59521640-59521882	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD1	chr11:59521587-59521897	GM12878	blood:	n/a	n/a
50	CHD2	chr11:59521552-59521755	HepG2	liver:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:59518964-59519014	Hela-S3	cervix:	n/a
2	chr11:59522827-59522877	SAEC	small airway:	n/a
3	chr11:59521722-59521772	ECC-1	luminal epithelium:	n/a
4	chr11:59525433-59525483	AG04449	skin:	fetal
5	chr11:59522542-59522592	NT2-D1	testis:	n/a
6	chr11:59522087-59522137	BJ	skin:	n/a
7	chr11:59521791-59521841	Hela-S3	cervix:	n/a
8	chr11:59522542-59522592	ECC-1	luminal epithelium:	n/a
9	chr11:59522827-59522877	HEEpiC	esophagus:	n/a
10	chr11:59521722-59521772	U87	brain:	n/a
11	chr11:59522827-59522877	LNCaP	prostate:	n/a
12	chr11:59522087-59522137	Hela-S3	cervix:	n/a
13	chr11:59522827-59522877	HMEC	breast:	n/a
14	chr11:59522917-59522967	SK-N-SH_RA	brain:	n/a
15	chr11:59521791-59521841	SK-N-SH	brain:	n/a
16	chr11:59525433-59525483	Caco-2	colon:	n/a
17	chr11:59522827-59522877	HNPCEpiC	eye:	n/a
18	chr11:59525433-59525483	SAEC	small airway:	n/a
19	chr11:59523120-59523170	ECC-1	luminal epithelium:	n/a
20	chr11:59518964-59519014	SK-N-SH	brain:	n/a
21	chr11:59522827-59522877	HCM	heart:	n/a
22	chr11:59523120-59523170	BJ	skin:	n/a
23	chr11:59523399-59523449	AG09319	gingival:	n/a
24	chr11:59522827-59522877	HIPEpiC	eye:	n/a
25	chr11:59523399-59523449	PrEC	prostate:	n/a
26	chr11:59522827-59522877	SK-N-MC	brain:	n/a
27	chr11:59523120-59523170	LNCaP	prostate:	n/a
28	chr11:59523120-59523170	HL-60	blood:	n/a
29	chr11:59522087-59522137	MCF-7	breast:	n/a
30	chr11:59523399-59523449	PANC-1	pancreas:	n/a
31	chr11:59522542-59522592	ProgFib	skin:	n/a
32	chr11:59523120-59523170	HepG2	liver:	n/a
33	chr11:59521722-59521772	A549	lung:	n/a
34	chr11:59522827-59522877	H1-hESC	embryonic stem cell:	embryo
35	chr11:59521665-59521715	SAEC	small airway:	n/a
36	chr11:59518964-59519014	HCT-116	colon:	n/a
37	chr11:59522542-59522592	CMK	blood:	n/a
38	chr11:59522542-59522592	PrEC	prostate:	n/a
39	chr11:59521665-59521715	ECC-1	luminal epithelium:	n/a
40	chr11:59521722-59521772	HCPEpiC	choroid plexus:	n/a
41	chr11:59525433-59525483	GM19239	blood:	n/a
42	chr11:59522822-59522872	SAEC	small airway:	n/a
43	chr11:59521665-59521715	HNPCEpiC	eye:	n/a
44	chr11:59525433-59525483	HCM	heart:	n/a
45	chr11:59523399-59523449	HRPEpiC	eye:	n/a
46	chr11:59522917-59522967	GM19239	blood:	n/a
47	chr11:59518964-59519014	BE2_C	brain:	n/a
48	chr11:59522822-59522872	AG09309	skin:	n/a
49	chr11:59522542-59522592	HCT-116	colon:	n/a
50	chr11:59523399-59523449	HepG2	liver:	n/a

(count:49 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:114300956..114303148-chr11:59521456..59522999,2	MCF-7	breast:
2	chr11:59520214..59524923-chr11:59576549..59579669,4	MCF-7	breast:
3	chr11:59434314..59436454-chr11:59523129..59524749,2	MCF-7	breast:
4	chr1:114301552..114304210-chr11:59521950..59524919,2	MCF-7	breast:
5	chr11:59512620..59514744-chr11:59515502..59517848,2	K562	blood:
6	chr11:59521565..59522093-chr11:59577744..59578503,3	K562	blood:
7	chr11:59435275..59437958-chr11:59523274..59525120,2	K562	blood:
8	chr11:59434813..59437700-chr11:59529153..59532130,2	K562	blood:
9	chr11:59520935..59525781-chr11:59552803..59557885,8	MCF-7	breast:
10	chr11:59519722..59526041-chr11:59575307..59578961,7	MCF-7	breast:
11	chr11:59479954..59482315-chr11:59521677..59523287,2	K562	blood:
12	chr11:59522643..59524451-chr16:67197812..67200302,2	MCF-7	breast:
13	chr11:59528800..59530439-chr11:59536843..59538361,2	K562	blood:
14	chr11:59514703..59516740-chr11:59522091..59524203,2	MCF-7	breast:
15	chr11:59528968..59531092-chr11:59531275..59534785,3	MCF-7	breast:
16	chr11:59520651..59522378-chr11:59577196..59579780,2	K562	blood:
17	chr11:59507824..59511507-chr11:59512548..59517699,5	K562	blood:
18	chr11:59524342..59526503-chr11:59895914..59898117,2	K562	blood:
19	chr11:59517040..59519378-chr11:59520146..59522699,3	K562	blood:
20	chr11:59520634..59522259-chr11:59568757..59570737,15	MCF-7	breast:
21	chr11:59524561..59526544-chr11:59527654..59529309,2	K562	blood:
22	chr11:59483722..59486597-chr11:59487703..59490469,2	K562	blood:
23	chr11:59491083..59492965-chr11:59516248..59517862,2	K562	blood:
24	chr11:59524470..59526644-chr11:59576559..59579477,2	K562	blood:
25	chr11:59435116..59437063-chr11:59524775..59526282,2	MCF-7	breast:
26	chr11:59523011..59526082-chr11:59538557..59541399,3	K562	blood:
27	chr11:59381725..59384642-chr11:59521273..59522941,2	K562	blood:
28	chr11:59501872..59503940-chr11:59513222..59515810,2	K562	blood:
29	chr11:59521183..59522129-chr11:59897665..59898553,3	K562	blood:
30	chr11:59527108..59529447-chr11:59575542..59578069,2	K562	blood:
31	chr11:59434813..59437700-chr11:59527969..59532130,3	K562	blood:
32	chr11:59507824..59511507-chr11:59512548..59517699,5	K562	blood:
33	chr11:59436132..59436823-chr11:59522370..59523215,2	Hela-S3	cervix:
34	chr11:59525592..59530085-chr11:59541874..59544413,4	MCF-7	breast:
35	chr11:59521037..59522134-chr11:59569735..59571070,7	MCF-7	breast:
36	chr11:59507173..59508866-chr11:59509894..59511921,2	MCF-7	breast:
37	chr11:59338335..59341054-chr11:59523391..59525087,2	K562	blood:
38	chr11:59480505..59482058-chr11:59521372..59523220,2	MCF-7	breast:
39	chr11:59514703..59516740-chr11:59522091..59524203,2	MCF-7	breast:
40	chr11:59524086..59527100-chr11:59562036..59566257,3	K562	blood:
41	chr11:59521347..59522076-chr11:59577896..59578446,2	MCF-7	breast:
42	chr11:59521605..59525070-chr11:59543036..59549785,6	MCF-7	breast:
43	chr11:59521192..59521888-chr11:59568592..59569530,2	MCF-7	breast:
44	chr11:59524561..59526544-chr11:59527654..59529309,2	K562	blood:
45	chr11:59513939..59516832-chr11:59518797..59521533,2	K562	blood:
46	chr11:59521189..59522029-chr11:59569757..59570741,3	K562	blood:
47	chr11:59501872..59503940-chr11:59513222..59515810,2	K562	blood:
48	chr11:59515464..59518097-chr11:59523433..59525658,2	K562	blood:
49	chr11:59527952..59530580-chr11:59535251..59538243,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AP000790.1-6	chr11:59508798-59509522	NONHSAT021541
2	lnc-OR10V1-1	chr11:59521753-59522448	ENSG00000254477.1
3	lnc-OR10V1-1	chr11:59520488-59520670	ENSG00000254477.1

No data

Variant related genes	Relation type
OR10V2P	TF binding region
OR10V3P	TF binding region
OR10Y1P	TF binding region
STX3	TF binding region
ENSG00000254477	TF binding region
OR10V2P	CpG island
OR10V3P	CpG island
OR10Y1P	CpG island
STX3	CpG island
ENSG00000254477	CpG island
ENSG00000255139	chromatin interactions
ENSG00000116793	chromatin interactions
ENSG00000166902	chromatin interactions
ENSG00000166900	chromatin interactions
ENSG00000254477	chromatin interactions
ENSG00000234964	chromatin interactions
ENSG00000102878	chromatin interactions
ENSG00000254743	chromatin interactions
ENSG00000166889	chromatin interactions
ENSG00000255355	chromatin interactions
ENSG00000265690	chromatin interactions
ENSG00000172289	chromatin interactions
ENSG00000255538	chromatin interactions
ENSG00000110048	chromatin interactions

Extended variants
information (count: 1320 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:1320 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552649886	chr11:59490462-59490463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs189007082	chr11:59490555-59490556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs117492701	chr11:59490607-59490608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs562917487	chr11:59490611-59490612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs569364778	chr11:59490621-59490622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs533607418	chr11:59490647-59490648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs545214205	chr11:59490672-59490673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs553310549	chr11:59490749-59490750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs538375461	chr11:59490770-59490771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560186909	chr11:59490777-59490778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs540989	chr11:59490818-59490819	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs193149489	chr11:59490820-59490821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs140566147	chr11:59490880-59490881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567363791	chr11:59490914-59490915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs148312520	chr11:59490917-59490918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs550078669	chr11:59490920-59490921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs556826087	chr11:59490988-59490989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538798293	chr11:59491005-59491006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs184259370	chr11:59491010-59491011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs568268627	chr11:59491039-59491040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs189205199	chr11:59491059-59491060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs536390465	chr11:59491085-59491086	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs34702936	chr11:59491108-59491109	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs370093305	chr11:59491140-59491141	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs554598171	chr11:59491161-59491162	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs508411	chr11:59491263-59491264	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs112916340	chr11:59491293-59491294	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs556783243	chr11:59491354-59491355	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs544392340	chr11:59491389-59491390	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs150815856	chr11:59491425-59491426	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs545154435	chr11:59491438-59491439	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs560326289	chr11:59491456-59491457	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs111359566	chr11:59491488-59491489	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs111503770	chr11:59491489-59491490	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs572197987	chr11:59491613-59491614	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs11230061	chr11:59491673-59491674	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs545393395	chr11:59491689-59491690	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs528961567	chr11:59491692-59491693	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs561105884	chr11:59491723-59491724	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs191659301	chr11:59491728-59491729	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs575718283	chr11:59491803-59491804	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs370017196	chr11:59491813-59491814	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs549927853	chr11:59491879-59491880	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs138137716	chr11:59491895-59491896	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs7111932	chr11:59491994-59491995	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs143863781	chr11:59492053-59492054	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs547604759	chr11:59492075-59492076	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs147325049	chr11:59492086-59492087	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs536327893	chr11:59492123-59492124	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs537625	chr11:59492132-59492133	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:51)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Autism	22495309	CNVD
Autism	20808228	CNVD
Acute lymphoblastic leukemia	21339820	CNVD

Chromatin state (count:775 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:59490200-59491600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr11:59491400-59491800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr11:59491600-59491800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr11:59491800-59496400	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr11:59494800-59495000	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr11:59494800-59495400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr11:59495000-59495600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr11:59495000-59496800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr11:59495200-59499000	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr11:59495400-59496400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr11:59495600-59496000	Enhancers	Monocytes-CD14+_RO01746	blood
12	chr11:59495600-59496200	Enhancers	Stomach Mucosa	stomach
13	chr11:59495600-59497000	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr11:59495800-59496000	Enhancers	Fetal Intestine Small	intestine
15	chr11:59495800-59496800	Enhancers	K562	blood
16	chr11:59495800-59497400	Enhancers	Primary hematopoietic stem cells	blood
17	chr11:59496000-59496600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
18	chr11:59496000-59496800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr11:59496000-59496800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
20	chr11:59496000-59497000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
21	chr11:59496200-59496800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr11:59496200-59496800	Enhancers	NHEK	skin
23	chr11:59496200-59497000	Enhancers	HUVEC	blood vessel
24	chr11:59496400-59496800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr11:59496400-59496800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
26	chr11:59496400-59496800	Enhancers	Primary T cells fromperipheralblood	blood
27	chr11:59496400-59496800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr11:59496400-59496800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr11:59496400-59496800	Enhancers	HMEC	breast
30	chr11:59496800-59497200	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr11:59496800-59497200	Enhancers	Monocytes-CD14+_RO01746	blood
32	chr11:59496800-59498800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr11:59497200-59497600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
34	chr11:59497200-59498000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
35	chr11:59497600-59499000	Enhancers	Monocytes-CD14+_RO01746	blood
36	chr11:59497800-59500400	Enhancers	Fetal Intestine Large	intestine
37	chr11:59497800-59500800	Enhancers	Fetal Intestine Small	intestine
38	chr11:59498000-59499400	Enhancers	Primary neutrophils fromperipheralblood	blood
39	chr11:59498200-59498400	Enhancers	Fetal Kidney	kidney
40	chr11:59498400-59499000	Enhancers	HepG2	liver
41	chr11:59498600-59498800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr11:59498600-59502800	Weak transcription	Fetal Kidney	kidney
43	chr11:59498800-59499400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr11:59498800-59499400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr11:59499400-59500400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr11:59499400-59502000	Weak transcription	Primary neutrophils fromperipheralblood	blood
47	chr11:59499400-59504400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr11:59499800-59500400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr11:59501000-59501200	Enhancers	Placenta	Placenta
50	chr11:59501800-59502000	Enhancers	Placenta	Placenta

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