Variant report

Variant	nsv825855
Chromosome Location	chr11:45167783-45168824
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:523)
CpG islands
(count:183)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:523 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:45167670-45167842	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:45168717-45169083	HepG2	liver:	n/a	n/a
3	ATF1	chr11:45168645-45168977	K562	blood:	n/a	n/a
4	ATF3	chr11:45168339-45168512	K562	blood:	n/a	n/a
5	ATF3	chr11:45168614-45168859	K562	blood:	n/a	chr11:45168842-45168851
6	ATF3	chr11:45168695-45168861	K562	blood:	n/a	chr11:45168842-45168851
7	BACH1	chr11:45168731-45169234	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCLAF1	chr11:45168582-45168978	GM12878	blood:	n/a	chr11:45168879-45168892 chr11:45168876-45168889 chr11:45168878-45168891 chr11:45168926-45168939
9	BHLHE40	chr11:45168744-45168826	K562	blood:	n/a	n/a
10	BHLHE40	chr11:45168651-45168966	GM12878	blood:	n/a	chr11:45168921-45168937 chr11:45168918-45168934 chr11:45168915-45168931
11	BRCA1	chr11:45168649-45169275	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr11:45168734-45169265	HepG2	liver:	n/a	n/a
13	BRCA1	chr11:45167471-45168136	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr11:45168605-45168942	K562	blood:	n/a	n/a
15	CCNT2	chr11:45168019-45169060	K562	blood:	n/a	n/a
16	CEBPB	chr11:45168084-45169567	Hela-S3	cervix:	n/a	n/a
17	CEBPD	chr11:45168584-45168994	HepG2	liver:	n/a	n/a
18	CEBPD	chr11:45168000-45168259	HepG2	liver:	n/a	n/a
19	CHD1	chr11:45167584-45168292	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD1	chr11:45168678-45168892	GM12878	blood:	n/a	chr11:45168843-45168853
21	CHD2	chr11:45168266-45168273	K562	blood:	n/a	n/a
22	CHD2	chr11:45168635-45169095	HepG2	liver:	n/a	chr11:45168843-45168853
23	CHD2	chr11:45168631-45169064	K562	blood:	n/a	chr11:45168843-45168853
24	CHD2	chr11:45167681-45169502	Hela-S3	cervix:	n/a	chr11:45168843-45168853
25	CHD2	chr11:45168613-45169191	GM12878	blood:	n/a	chr11:45168843-45168853
26	CHD2	chr11:45168599-45169203	H1-hESC	embryonic stem cell:	n/a	chr11:45168843-45168853
27	CREB1	chr11:45168617-45169113	K562	blood:	n/a	n/a
28	CREB1	chr11:45168594-45169177	HepG2	liver:	n/a	n/a
29	CREB1	chr11:45168608-45169050	K562	blood:	n/a	n/a
30	CREB1	chr11:45168557-45169269	H1-hESC	embryonic stem cell:	n/a	n/a
31	CREB1	chr11:45168588-45169173	H1-hESC	embryonic stem cell:	n/a	n/a
32	CREB1	chr11:45168566-45169203	A549	lung:	n/a	n/a
33	CREB1	chr11:45168618-45168947	A549	lung:	n/a	n/a
34	CREB1	chr11:45168629-45168951	ECC-1	luminal epithelium:	n/a	n/a
35	CREB1	chr11:45168485-45169102	GM12878	blood:	n/a	n/a
36	CREB1	chr11:45167955-45168523	A549	lung:	n/a	n/a
37	CREB1	chr11:45167921-45169395	HepG2	liver:	n/a	n/a
38	CTCF	chr11:45168780-45168908	Kidney_OC	kidney:	n/a	n/a
39	CTCF	chr11:45168120-45168270	AG04449	skin:	n/a	n/a
40	CTCF	chr11:45168813-45168919	GM12892	blood:	n/a	n/a
41	CTCF	chr11:45168720-45168891	GM12878	blood:	n/a	n/a
42	CTCF	chr11:45168770-45168855	Lung_OC	lung:	n/a	n/a
43	CTCF	chr11:45168600-45168750	GM12868	blood:	n/a	n/a
44	CTCF	chr11:45168740-45168890	AG04449	skin:	n/a	n/a
45	CTCF	chr11:45168720-45168870	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr11:45168733-45169044	K562	blood:	n/a	n/a
47	CTCF	chr11:45168740-45168890	GM12865	blood:	n/a	n/a
48	CTCF	chr11:45168820-45169090	HUVEC	blood vessel:	n/a	n/a
49	CTCF	chr11:45168740-45168890	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr11:45168782-45168787	Pancreas_OC	pancreas:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:45168563-45168613	Hela-S3	cervix:	n/a
2	chr11:45167772-45167822	Caco-2	colon:	n/a
3	chr11:45168563-45168613	IMR90	lung:	fetal
4	chr11:45168563-45168613	HMEC	breast:	n/a
5	chr11:45167805-45167855	AG10803	skin:	n/a
6	chr11:45168563-45168613	ProgFib	skin:	n/a
7	chr11:45167772-45167822	T-47D	breast:	n/a
8	chr11:45167772-45167822	HRE	kidney:	n/a
9	chr11:45168563-45168613	GM19239	blood:	n/a
10	chr11:45167805-45167855	AG09309	skin:	n/a
11	chr11:45168563-45168613	AG09309	skin:	n/a
12	chr11:45168563-45168613	Jurkat	blood:	n/a
13	chr11:45167805-45167855	HUVEC	blood vessel:	n/a
14	chr11:45168563-45168613	ECC-1	luminal epithelium:	n/a
15	chr11:45167772-45167822	PFSK-1	brain:	n/a
16	chr11:45168563-45168613	H1-hESC	embryonic stem cell:	embryo
17	chr11:45168563-45168613	BE2_C	brain:	n/a
18	chr11:45167772-45167822	ProgFib	skin:	n/a
19	chr11:45168563-45168613	HEEpiC	esophagus:	n/a
20	chr11:45167772-45167822	GM12878	blood:	n/a
21	chr11:45167805-45167855	SKMC	muscle:	n/a
22	chr11:45167805-45167855	GM19239	blood:	n/a
23	chr11:45168563-45168613	HIPEpiC	eye:	n/a
24	chr11:45167805-45167855	PFSK-1	brain:	n/a
25	chr11:45167805-45167855	HIPEpiC	eye:	n/a
26	chr11:45167772-45167822	HPAEpiC	pulmonary alveolar:	n/a
27	chr11:45167772-45167822	HCM	heart:	n/a
28	chr11:45167772-45167822	AG09309	skin:	n/a
29	chr11:45167805-45167855	GM12892	blood:	n/a
30	chr11:45167772-45167822	HCT-116	colon:	n/a
31	chr11:45167772-45167822	HEK293	kidney:	embryo
32	chr11:45167772-45167822	GM19239	blood:	n/a
33	chr11:45167805-45167855	H1-hESC	embryonic stem cell:	embryo
34	chr11:45167805-45167855	HMEC	breast:	n/a
35	chr11:45167805-45167855	NHBE	bronchial:	n/a
36	chr11:45167772-45167822	MCF-7	breast:	n/a
37	chr11:45167772-45167822	ovcar-3	ovarian:	n/a
38	chr11:45168563-45168613	RPTEC	kidney:	n/a
39	chr11:45167805-45167855	HCM	heart:	n/a
40	chr11:45168563-45168613	HPAEpiC	pulmonary alveolar:	n/a
41	chr11:45167772-45167822	K562	blood:	n/a
42	chr11:45167805-45167855	HCF	heart:	n/a
43	chr11:45167772-45167822	AG04449	skin:	fetal
44	chr11:45167772-45167822	SAEC	small airway:	n/a
45	chr11:45167805-45167855	HNPCEpiC	eye:	n/a
46	chr11:45167772-45167822	Hepatocyte	liver:	n/a
47	chr11:45167772-45167822	HRPEpiC	eye:	n/a
48	chr11:45167772-45167822	RPTEC	kidney:	n/a
49	chr11:45167772-45167822	PrEC	prostate:	n/a
50	chr11:45168563-45168613	HCF	heart:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:44971020..44974752-chr11:45167266..45169322,3	MCF-7	breast:
2	chr1:228352747..228353404-chr11:45167742..45168503,2	Hela-S3	cervix:
3	chr11:45167998..45168767-chr5:56205154..56205766,2	Hela-S3	cervix:
4	chr10:70747303..70749893-chr11:45167896..45169684,2	MCF-7	breast:
5	chr11:45167893..45171206-chr11:45200303..45204446,5	MCF-7	breast:
6	chr11:45168231..45168959-chr2:96810761..96811512,2	Hela-S3	cervix:
7	chr11:45164160..45171283-chr11:45198764..45207868,26	MCF-7	breast:
8	chr11:45167440..45169930-chr11:45202656..45204248,2	K562	blood:
9	chr11:44940135..44943122-chr11:45165602..45168415,2	MCF-7	breast:
10	chr11:45168582..45169343-chr6:26157874..26158814,2	HCT-116	colon:

No data

Variant related genes	Relation type
PRDM11	TF binding region
PRDM11	CpG island
ENSG00000158373	chromatin interactions
ENSG00000175274	chromatin interactions
ENSG00000155542	chromatin interactions
ENSG00000203684	chromatin interactions
ENSG00000158050	chromatin interactions
ENSG00000198954	chromatin interactions
ENSG00000019485	chromatin interactions
ENSG00000157570	chromatin interactions

Extended variants
information (count: 41 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:41 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552540807	chr11:45167819-45167820	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs562136862	chr11:45167823-45167824	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs372000061	chr11:45167831-45167832	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs138469892	chr11:45167860-45167861	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs564818529	chr11:45167900-45167901	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs376755971	chr11:45167908-45167909	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs183034822	chr11:45167937-45167938	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs200594641	chr11:45167949-45167950	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs551759847	chr11:45167953-45167954	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs377045507	chr11:45167966-45167967	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs111917794	chr11:45167972-45167973	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs185818306	chr11:45167993-45167994	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs537538380	chr11:45168031-45168032	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs548312756	chr11:45168049-45168050	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs568146050	chr11:45168054-45168055	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs11038329	chr11:45168061-45168062	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs201820352	chr11:45168068-45168069	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs553752982	chr11:45168112-45168113	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs2863154	chr11:45168124-45168125	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs539801072	chr11:45168147-45168148	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs12790910	chr11:45168182-45168183	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs556585915	chr11:45168228-45168229	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs373991513	chr11:45168232-45168233	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs144041532	chr11:45168258-45168259	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs542386479	chr11:45168264-45168265	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs542319438	chr11:45168307-45168308	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs190194785	chr11:45168314-45168315	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs7483388	chr11:45168327-45168328	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs572515548	chr11:45168406-45168407	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs541634130	chr11:45168610-45168611	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs182926434	chr11:45168612-45168613	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs533457160	chr11:45168613-45168614	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs550100901	chr11:45168678-45168679	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs373547951	chr11:45168680-45168681	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs2171430	chr11:45168681-45168682	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs562141874	chr11:45168713-45168714	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs140980768	chr11:45168738-45168739	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs547942411	chr11:45168744-45168745	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs187500627	chr11:45168746-45168747	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs568167733	chr11:45168783-45168784	Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs556809983	chr11:45168802-45168803	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Parathyroid adenoma	22454399	CNVD
Medulloblastoma	21979893	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21364760	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Intracranial ependymoma	16609018	CNVD
Myxofibrosarcoma	16751306	CNVD
Potocki-Shaffer syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Breast cancer	20409316	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:232 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:45166800-45167800	Flanking Active TSS	Brain Hippocampus Middle	brain
2	chr11:45166800-45168200	Enhancers	Spleen	Spleen
3	chr11:45166800-45169600	Active TSS	H9 Cell Line	embryonic stem cell
4	chr11:45167000-45167800	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
5	chr11:45167000-45167800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr11:45167000-45167800	Flanking Active TSS	Brain Anterior Caudate	brain
7	chr11:45167000-45167800	Enhancers	Gastric	stomach
8	chr11:45167000-45168000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr11:45167000-45168000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
10	chr11:45167200-45167800	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr11:45167200-45167800	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr11:45167200-45167800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr11:45167200-45167800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr11:45167200-45167800	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
15	chr11:45167200-45167800	Flanking Active TSS	Brain Cingulate Gyrus	brain
16	chr11:45167200-45167800	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
17	chr11:45167200-45167800	Flanking Active TSS	Brain Substantia Nigra	brain
18	chr11:45167200-45167800	Flanking Active TSS	Colon Smooth Muscle	Colon
19	chr11:45167200-45167800	Flanking Active TSS	Duodenum Mucosa	Duodenum
20	chr11:45167200-45167800	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
21	chr11:45167200-45167800	Enhancers	Fetal Heart	heart
22	chr11:45167200-45167800	Flanking Active TSS	Fetal Intestine Small	intestine
23	chr11:45167200-45167800	Enhancers	Lung	lung
24	chr11:45167200-45167800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
25	chr11:45167200-45167800	Flanking Active TSS	Rectal Smooth Muscle	rectum
26	chr11:45167200-45167800	Enhancers	Sigmoid Colon	Sigmoid Colon
27	chr11:45167200-45167800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
28	chr11:45167200-45167800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
29	chr11:45167200-45167800	Flanking Active TSS	HSMMtube	muscle
30	chr11:45167200-45168000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr11:45167200-45168000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
32	chr11:45167200-45168000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
33	chr11:45167200-45168000	Flanking Active TSS	Liver	Liver
34	chr11:45167200-45168000	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
35	chr11:45167200-45168200	Flanking Bivalent TSS/Enh	Dnd41	blood
36	chr11:45167200-45169200	Active TSS	H1 Cell Line	embryonic stem cell
37	chr11:45167200-45169200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr11:45167200-45169200	Active TSS	Fetal Kidney	kidney
39	chr11:45167200-45169600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr11:45167200-45169800	Active TSS	ES-I3 Cell Line	embryonic stem cell
41	chr11:45167200-45170000	Active TSS	Pancreatic Islets	Pancreatic Islet
42	chr11:45167400-45167800	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr11:45167400-45167800	Flanking Bivalent TSS/Enh	Primary monocytes fromperipheralblood	blood
44	chr11:45167400-45167800	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
45	chr11:45167400-45167800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
46	chr11:45167400-45167800	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
47	chr11:45167400-45167800	Flanking Bivalent TSS/Enh	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr11:45167400-45167800	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
49	chr11:45167400-45167800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr11:45167400-45167800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin

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