Variant report

Variant	nsv975155
Chromosome Location	chr11:17247352-17252105
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr11:17251783-17252811	GM12878	blood:	n/a	n/a
2	BRCA1	chr11:17251642-17252019	Hela-S3	cervix:	n/a	n/a
3	CTCF	chr11:17251760-17251910	Hela-S3	cervix:	n/a	chr11:17251813-17251831 chr11:17251815-17251836 chr11:17251816-17251829
4	CTCF	chr11:17251483-17252272	HCT-116	colon:	n/a	chr11:17251813-17251831 chr11:17251815-17251836 chr11:17251816-17251829
5	CTCF	chr11:17251613-17251954	Pancreas_OC	pancreas:	n/a	chr11:17251813-17251831 chr11:17251815-17251836 chr11:17251816-17251829
6	CTCF	chr11:17251760-17251910	GM12871	blood:	n/a	chr11:17251813-17251831 chr11:17251815-17251836 chr11:17251816-17251829
7	CTCF	chr11:17251674-17251965	SK-N-SH_RA	brain:	n/a	chr11:17251813-17251831 chr11:17251815-17251836 chr11:17251816-17251829
8	CTCF	chr11:17251638-17251999	A549	lung:	n/a	chr11:17251813-17251831 chr11:17251815-17251836 chr11:17251816-17251829
9	CTCF	chr11:17251820-17251970	HMEC	breast:	n/a	n/a
10	CTCF	chr11:17251740-17251890	AG09309	skin:	n/a	chr11:17251813-17251831 chr11:17251815-17251836 chr11:17251816-17251829
11	CTCF	chr11:17251722-17251884	GM20000	blood:	n/a	chr11:17251813-17251831 chr11:17251815-17251836 chr11:17251816-17251829
12	CTCF	chr11:17248357-17248400	GM10266	blood:	n/a	n/a
13	CTCF	chr11:17251701-17251927	HepG2	liver:	n/a	chr11:17251813-17251831 chr11:17251815-17251836 chr11:17251816-17251829
14	CTCF	chr11:17251733-17251824	MCF-7	breast:	n/a	n/a
15	CTCF	chr11:17251716-17251911	GM13976	blood:	n/a	chr11:17251813-17251831 chr11:17251815-17251836 chr11:17251816-17251829
16	CTCF	chr11:17251720-17251870	GM12871	blood:	n/a	chr11:17251813-17251831 chr11:17251815-17251836 chr11:17251816-17251829
17	CTCF	chr11:17251760-17251910	HMEC	breast:	n/a	chr11:17251813-17251831 chr11:17251815-17251836 chr11:17251816-17251829
18	CTCF	chr11:17251420-17251570	SAEC	small airway:	n/a	n/a
19	CTCF	chr11:17251740-17251890	HRE	kidney:	n/a	chr11:17251813-17251831 chr11:17251815-17251836 chr11:17251816-17251829
20	CTCF	chr11:17251680-17251830	WI-38	lung:	n/a	chr11:17251816-17251829
21	CTCF	chr11:17251724-17251818	MCF-7	breast:	n/a	n/a
22	CTCF	chr11:17251585-17251942	K562	blood:	n/a	chr11:17251813-17251831 chr11:17251815-17251836 chr11:17251816-17251829
23	CTCF	chr11:17251760-17251910	SAEC	small airway:	n/a	chr11:17251813-17251831 chr11:17251815-17251836 chr11:17251816-17251829
24	CTCF	chr11:17251780-17251930	GM12878	blood:	n/a	chr11:17251813-17251831 chr11:17251815-17251836 chr11:17251816-17251829
25	CTCF	chr11:17251510-17251812	GM12891	blood:	n/a	n/a
26	CTCF	chr11:17251740-17251890	MCF-7	breast:	n/a	chr11:17251813-17251831 chr11:17251815-17251836 chr11:17251816-17251829
27	CTCF	chr11:17251723-17251841	GM19239	blood:	n/a	chr11:17251813-17251831 chr11:17251815-17251836 chr11:17251816-17251829
28	CTCF	chr11:17251638-17251945	A549	lung:	n/a	chr11:17251813-17251831 chr11:17251815-17251836 chr11:17251816-17251829
29	CTCF	chr11:17251780-17251930	HEEpiC	esophagus:	n/a	chr11:17251813-17251831 chr11:17251815-17251836 chr11:17251816-17251829
30	CTCF	chr11:17251420-17251570	HCM	heart:	n/a	n/a
31	CTCF	chr11:17251820-17251970	BE2_C	brain:	n/a	n/a
32	CTCF	chr11:17251369-17252216	A549	lung:	n/a	chr11:17251813-17251831 chr11:17251815-17251836 chr11:17251816-17251829
33	CTCF	chr11:17251740-17251890	AoAF	blood vessel:	n/a	chr11:17251813-17251831 chr11:17251815-17251836 chr11:17251816-17251829
34	CTCF	chr11:17251680-17251961	Medullo	brain:	n/a	chr11:17251813-17251831 chr11:17251815-17251836 chr11:17251816-17251829
35	CTCF	chr11:17251760-17251910	HCM	heart:	n/a	chr11:17251813-17251831 chr11:17251815-17251836 chr11:17251816-17251829
36	CTCF	chr11:17251760-17251910	NHDF-neo	bronchial:	n/a	chr11:17251813-17251831 chr11:17251815-17251836 chr11:17251816-17251829
37	CTCF	chr11:17251490-17251596	GM19238	blood:	n/a	n/a
38	CTCF	chr11:17251780-17251930	GM12873	blood:	n/a	chr11:17251813-17251831 chr11:17251815-17251836 chr11:17251816-17251829
39	CTCF	chr11:17251720-17251870	GM12870	blood:	n/a	chr11:17251813-17251831 chr11:17251815-17251836 chr11:17251816-17251829
40	CTCF	chr11:17251760-17251910	Caco-2	colon:	n/a	chr11:17251813-17251831 chr11:17251815-17251836 chr11:17251816-17251829
41	CTCF	chr11:17251760-17251910	RPTEC	kidney:	n/a	chr11:17251813-17251831 chr11:17251815-17251836 chr11:17251816-17251829
42	CTCF	chr11:17251360-17251510	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr11:17251720-17251870	MCF-7	breast:	n/a	chr11:17251813-17251831 chr11:17251815-17251836 chr11:17251816-17251829
44	CTCF	chr11:17251697-17251983	HUVEC	blood vessel:	n/a	chr11:17251813-17251831 chr11:17251815-17251836 chr11:17251816-17251829
45	CTCF	chr11:17251780-17251930	GM12870	blood:	n/a	chr11:17251813-17251831 chr11:17251815-17251836 chr11:17251816-17251829
46	CTCF	chr11:17251780-17251930	SK-N-SH_RA	brain:	n/a	chr11:17251813-17251831 chr11:17251815-17251836 chr11:17251816-17251829
47	CTCF	chr11:17251260-17251410	GM12873	blood:	n/a	n/a
48	CTCF	chr11:17251760-17251910	GM12865	blood:	n/a	chr11:17251813-17251831 chr11:17251815-17251836 chr11:17251816-17251829
49	CTCF	chr11:17251740-17251890	NHLF	lung:	n/a	chr11:17251813-17251831 chr11:17251815-17251836 chr11:17251816-17251829
50	CTCF	chr11:17251760-17251910	BJ	skin:	n/a	chr11:17251813-17251831 chr11:17251815-17251836 chr11:17251816-17251829

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:17251956-17252006	PANC-1	pancreas:	n/a
2	chr11:17251956-17252006	PANC-1	pancreas:	n/a
3	chr11:17249967-17250017	ProgFib	skin:	n/a
4	chr11:17251956-17252006	HAEpiC	amniotic membrane:	n/a
5	chr11:17249882-17249932	HPAEpiC	pulmonary alveolar:	n/a
6	chr11:17249882-17249932	SAEC	small airway:	n/a
7	chr11:17249967-17250017	MCF10A-Er-Src	breast:	n/a
8	chr11:17249882-17249932	ProgFib	skin:	n/a
9	chr11:17251956-17252006	HRE	kidney:	n/a
10	chr11:17249882-17249932	NB4	blood:	n/a
11	chr11:17249958-17250008	A549	lung:	n/a
12	chr11:17248467-17248517	BJ	skin:	n/a
13	chr11:17248467-17248517	HepG2	liver:	n/a
14	chr11:17251956-17252006	GM12878	blood:	n/a
15	chr11:17251956-17252006	NH-A	brain:	n/a
16	chr11:17249967-17250017	AG04449	skin:	fetal
17	chr11:17249967-17250017	RPTEC	kidney:	n/a
18	chr11:17248467-17248517	AG09309	skin:	n/a
19	chr11:17249882-17249932	SK-N-SH	brain:	n/a
20	chr11:17249882-17249932	NT2-D1	testis:	n/a
21	chr11:17251956-17252006	RPTEC	kidney:	n/a
22	chr11:17249958-17250008	U87	brain:	n/a
23	chr11:17248467-17248517	HMEC	breast:	n/a
24	chr11:17249958-17250008	PrEC	prostate:	n/a
25	chr11:17249967-17250017	Hepatocyte	liver:	n/a
26	chr11:17249958-17250008	LNCaP	prostate:	n/a
27	chr11:17251956-17252006	SAEC	small airway:	n/a
28	chr11:17248467-17248517	ECC-1	luminal epithelium:	n/a
29	chr11:17249958-17250008	MCF-7	breast:	n/a
30	chr11:17249967-17250017	H1-hESC	embryonic stem cell:	embryo
31	chr11:17249958-17250008	IMR90	lung:	fetal
32	chr11:17251956-17252006	SK-N-MC	brain:	n/a
33	chr11:17249958-17250008	HIPEpiC	eye:	n/a
34	chr11:17251956-17252006	SK-N-SH	brain:	n/a
35	chr11:17249958-17250008	Hepatocyte	liver:	n/a
36	chr11:17249967-17250017	PFSK-1	brain:	n/a
37	chr11:17249967-17250017	Hela-S3	cervix:	n/a
38	chr11:17249967-17250017	SK-N-SH	brain:	n/a
39	chr11:17249967-17250017	HEEpiC	esophagus:	n/a
40	chr11:17249958-17250008	HCF	heart:	n/a
41	chr11:17251956-17252006	HCPEpiC	choroid plexus:	n/a
42	chr11:17251956-17252006	GM19239	blood:	n/a
43	chr11:17249882-17249932	H1-hESC	embryonic stem cell:	embryo
44	chr11:17249958-17250008	HL-60	blood:	n/a
45	chr11:17251956-17252006	ProgFib	skin:	n/a
46	chr11:17249967-17250017	IMR90	lung:	fetal
47	chr11:17251956-17252006	AG10803	skin:	n/a
48	chr11:17249967-17250017	A549	lung:	n/a
49	chr11:17249958-17250008	AoSMC	blood vessel:	n/a
50	chr11:17249958-17250008	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:17251345..17252271-chr11:17549390..17549954,2	K562	blood:
2	chr11:17251338..17252303-chr11:17525826..17526790,3	K562	blood:
3	chr11:17251256..17252008-chr11:17375735..17376626,3	MCF-7	breast:
4	chr11:17251431..17252316-chr11:17372886..17373548,2	MCF-7	breast:
5	chr11:17251318..17252261-chr11:17405052..17406043,5	MCF-7	breast:
6	chr11:17251351..17251972-chr11:17410334..17410928,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000197149	TF binding region
ENSG00000197149	CpG island
ENSG00000188211	chromatin interactions
ENSG00000187486	chromatin interactions

Extended variants
information (count: 188 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:188 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561400383	chr11:17247355-17247356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs145404153	chr11:17247430-17247431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs187554866	chr11:17247469-17247470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs558210649	chr11:17247470-17247471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs147693977	chr11:17247471-17247472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs565519245	chr11:17247522-17247523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs140933279	chr11:17247591-17247592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs550705268	chr11:17247593-17247594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs562434972	chr11:17247599-17247600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs529736772	chr11:17247639-17247640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs548198344	chr11:17247646-17247647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs368753650	chr11:17247669-17247670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs7949699	chr11:17247708-17247709	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs534138649	chr11:17247732-17247733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs552038173	chr11:17247786-17247787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs150203488	chr11:17247789-17247790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs532758909	chr11:17247808-17247809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538710784	chr11:17247945-17247946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs562317313	chr11:17247981-17247982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs557053462	chr11:17248031-17248032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs192926746	chr11:17248069-17248070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs12280196	chr11:17248073-17248074	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs566954879	chr11:17248078-17248079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs554986989	chr11:17248117-17248118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs574288983	chr11:17248146-17248147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs541708783	chr11:17248159-17248160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs7101686	chr11:17248180-17248181	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs565439464	chr11:17248183-17248184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs57466818	chr11:17248277-17248278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs143830025	chr11:17248281-17248282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs7118443	chr11:17248286-17248287	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs57939905	chr11:17248318-17248319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs562550891	chr11:17248322-17248323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs529853138	chr11:17248336-17248337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs59432132	chr11:17248340-17248341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs547869605	chr11:17248341-17248342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs372939252	chr11:17248364-17248365	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs527550103	chr11:17248372-17248373	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs7101938	chr11:17248373-17248374	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs570281878	chr11:17248438-17248439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531377771	chr11:17248468-17248469	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
42	rs549598040	chr11:17248487-17248488	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
43	rs569000486	chr11:17248515-17248516	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
44	rs369102786	chr11:17248556-17248557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs554619101	chr11:17248587-17248588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs11605497	chr11:17248593-17248594	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs371683460	chr11:17248610-17248611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs534193755	chr11:17248713-17248714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs559314562	chr11:17248721-17248722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs56030249	chr11:17248746-17248747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	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
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Lung adenocarcinoma	17086460	CNVD
Urothelial cell carcinoma	18451213	CNVD
Lung cancer	17086460	CNVD
Uterine serous papillary cancer	19536090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:88 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:17232800-17251200	Weak transcription	Lung	lung
2	chr11:17233200-17251800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr11:17241000-17251600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr11:17243800-17248600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr11:17244400-17252000	Weak transcription	Primary hematopoietic stem cells	blood
6	chr11:17244800-17251800	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr11:17245200-17251800	Weak transcription	Hela-S3	cervix
8	chr11:17246600-17251000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr11:17246800-17247400	Enhancers	HUVEC	blood vessel
10	chr11:17246800-17251200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr11:17246800-17251400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr11:17246800-17251400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr11:17247000-17251400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr11:17247400-17251200	Weak transcription	HUVEC	blood vessel
15	chr11:17248600-17249600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr11:17249600-17250000	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr11:17250000-17252200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr11:17250800-17251600	Weak transcription	Monocytes-CD14+_RO01746	blood
19	chr11:17251000-17251800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr11:17251000-17252000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr11:17251200-17251800	Enhancers	Lung	lung
22	chr11:17251200-17251800	Enhancers	HUVEC	blood vessel
23	chr11:17251200-17251800	Weak transcription	NHEK	skin
24	chr11:17251200-17252200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr11:17251400-17251800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr11:17251400-17251800	Enhancers	Primary T helper cells PMA-I stimulated	--
27	chr11:17251400-17251800	Enhancers	Primary T killer memory cells from peripheral blood	blood
28	chr11:17251400-17251800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr11:17251400-17251800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr11:17251400-17251800	Enhancers	Dnd41	blood
31	chr11:17251600-17251800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr11:17251600-17251800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
33	chr11:17251600-17251800	Enhancers	Adipose Nuclei	Adipose
34	chr11:17251600-17251800	Enhancers	Brain Anterior Caudate	brain
35	chr11:17251600-17251800	Enhancers	Fetal Muscle Leg	muscle
36	chr11:17251600-17251800	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr11:17251600-17251800	Enhancers	NHDF-Ad	bronchial
38	chr11:17251600-17252000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr11:17251600-17252000	Enhancers	Right Atrium	heart
40	chr11:17251600-17252200	Enhancers	Duodenum Mucosa	Duodenum
41	chr11:17251600-17252200	Enhancers	Fetal Thymus	thymus
42	chr11:17251600-17253200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
43	chr11:17251800-17252000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr11:17251800-17252000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr11:17251800-17252000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr11:17251800-17252000	Enhancers	Brain Hippocampus Middle	brain
47	chr11:17251800-17252000	Enhancers	Brain Substantia Nigra	brain
48	chr11:17251800-17252000	Enhancers	Fetal Lung	lung
49	chr11:17251800-17252000	Enhancers	Rectal Mucosa Donor 31	rectum
50	chr11:17251800-17252000	Flanking Active TSS	A549	lung

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