Variant report

Variant	esv2421582
Chromosome Location	chr17:15642546-15677001
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:118)
CpG islands
(count:610)
Chromatin interactive
region (count:2)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:118 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr17:15643479-15643633	Hela-S3	cervix:	n/a	n/a
2	CEBPB	chr17:15643389-15643669	A549	lung:	n/a	n/a
3	CTCF	chr17:15643480-15643630	MCF-7	breast:	n/a	n/a
4	CTCF	chr17:15671235-15671316	GM13977	blood:	n/a	n/a
5	CTCF	chr17:15643480-15643630	NHEK	skin:	n/a	n/a
6	CTCF	chr17:15643500-15643650	HBMEC	blood vessel:	n/a	n/a
7	CTCF	chr17:15672261-15672504	MCF-7	breast:	n/a	n/a
8	CTCF	chr17:15642690-15642735	GM20000	blood:	n/a	n/a
9	CTCF	chr17:15668468-15668555	Lung_OC	lung:	n/a	n/a
10	CTCF	chr17:15672328-15672471	HepG2	liver:	n/a	n/a
11	CTCF	chr17:15643181-15643227	GM13976	blood:	n/a	n/a
12	CTCF	chr17:15672228-15672496	A549	lung:	n/a	n/a
13	CTCF	chr17:15643520-15643670	HEK293	kidney:	n/a	n/a
14	CTCF	chr17:15655194-15655285	GM13976	blood:	n/a	n/a
15	CTCF	chr17:15672277-15672498	Gliobla	brain:	n/a	n/a
16	CTCF	chr17:15672290-15672483	A549	lung:	n/a	n/a
17	CTCF	chr17:15643500-15643650	HEK293	kidney:	n/a	n/a
18	CTCF	chr17:15672440-15672590	SK-N-SH_RA	brain:	n/a	n/a
19	CTCF	chr17:15672282-15672499	GM12892	blood:	n/a	n/a
20	CTCF	chr17:15672291-15672439	LNCaP	prostate:	n/a	n/a
21	CTCF	chr17:15643520-15643670	HCPEpiC	choroid plexus:	n/a	n/a
22	CTCF	chr17:15643500-15643650	HPAF	blood vessel:	n/a	n/a
23	CTCF	chr17:15643520-15643670	HCFaa	heart:	n/a	n/a
24	CTCF	chr17:15672282-15672486	NHEK	skin:	n/a	n/a
25	CTCF	chr17:15666698-15666753	Spleen_OC	spleen:	n/a	n/a
26	CTCF	chr17:15672340-15672469	HUVEC	blood vessel:	n/a	n/a
27	CTCF	chr17:15672264-15672508	MCF-7	breast:	n/a	n/a
28	CTCF	chr17:15672060-15672210	HAc	cerebellar:	n/a	n/a
29	CTCF	chr17:15672330-15672420	GM19238	blood:	n/a	n/a
30	CTCF	chr17:15672278-15672492	MCF-7	breast:	n/a	n/a
31	CTCF	chr17:15643500-15643650	HCPEpiC	choroid plexus:	n/a	n/a
32	CTCF	chr17:15672270-15672499	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr17:15643500-15643650	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr17:15672365-15672431	GM19239	blood:	n/a	n/a
35	CTCF	chr17:15654856-15654909	GM13976	blood:	n/a	n/a
36	CTCF	chr17:15672282-15672486	GM12891	blood:	n/a	n/a
37	CTCF	chr17:15653545-15653592	GM13976	blood:	n/a	n/a
38	CTCF	chr17:15655205-15655263	GM13977	blood:	n/a	n/a
39	CTCF	chr17:15652603-15652660	A549	lung:	n/a	chr17:15652623-15652636
40	CTCF	chr17:15643500-15643650	MCF-7	breast:	n/a	n/a
41	CTCF	chr17:15672313-15672454	GM19240	blood:	n/a	n/a
42	CTCF	chr17:15643510-15643594	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr17:15672364-15672419	Medullo	brain:	n/a	n/a
44	CTCF	chr17:15672304-15672497	Pancreas_OC	pancreas:	n/a	n/a
45	CTCF	chr17:15672315-15672472	ProgFib	skin:	n/a	n/a
46	CTCF	chr17:15643133-15643184	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr17:15672366-15672430	K562	blood:	n/a	n/a
48	CTCF	chr17:15643440-15643590	HVMF	connective:	n/a	n/a
49	CTCF	chr17:15672311-15672497	Fibrobl	skin:	n/a	n/a
50	CTCF	chr17:15672262-15672511	MCF-7	breast:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:15653096-15653146	AG09319	gingival:	n/a
2	chr17:15644575-15644625	HRCEpiC	kidney:	n/a
3	chr17:15650385-15650435	SKMC	muscle:	n/a
4	chr17:15652329-15652379	MCF-7	breast:	n/a
5	chr17:15653548-15653598	RPTEC	kidney:	n/a
6	chr17:15653473-15653523	HMEC	breast:	n/a
7	chr17:15652715-15652765	Hela-S3	cervix:	n/a
8	chr17:15653473-15653523	HCF	heart:	n/a
9	chr17:15650385-15650435	HEEpiC	esophagus:	n/a
10	chr17:15644575-15644625	RPTEC	kidney:	n/a
11	chr17:15652329-15652379	AG09309	skin:	n/a
12	chr17:15650385-15650435	MCF10A-Er-Src	breast:	n/a
13	chr17:15644575-15644625	LNCaP	prostate:	n/a
14	chr17:15650385-15650435	MCF-7	breast:	n/a
15	chr17:15653548-15653598	LNCaP	prostate:	n/a
16	chr17:15646415-15646465	NT2-D1	testis:	n/a
17	chr17:15655637-15655687	A549	lung:	n/a
18	chr17:15652854-15652904	Jurkat	blood:	n/a
19	chr17:15653473-15653523	HRE	kidney:	n/a
20	chr17:15646415-15646465	SK-N-MC	brain:	n/a
21	chr17:15655637-15655687	GM12891	blood:	n/a
22	chr17:15652715-15652765	RPTEC	kidney:	n/a
23	chr17:15644575-15644625	MCF-7	breast:	n/a
24	chr17:15652854-15652904	NT2-D1	testis:	n/a
25	chr17:15652329-15652379	HCPEpiC	choroid plexus:	n/a
26	chr17:15646415-15646465	NB4	blood:	n/a
27	chr17:15653473-15653523	BJ	skin:	n/a
28	chr17:15653473-15653523	ECC-1	luminal epithelium:	n/a
29	chr17:15652715-15652765	NB4	blood:	n/a
30	chr17:15650385-15650435	AG09319	gingival:	n/a
31	chr17:15652854-15652904	PrEC	prostate:	n/a
32	chr17:15646415-15646465	NHBE	bronchial:	n/a
33	chr17:15644575-15644625	HCM	heart:	n/a
34	chr17:15646415-15646465	ECC-1	luminal epithelium:	n/a
35	chr17:15653096-15653146	HepG2	liver:	n/a
36	chr17:15653473-15653523	IMR90	lung:	fetal
37	chr17:15653096-15653146	AG09309	skin:	n/a
38	chr17:15652854-15652904	U87	brain:	n/a
39	chr17:15653548-15653598	AG09319	gingival:	n/a
40	chr17:15655637-15655687	GM06990	blood:	n/a
41	chr17:15646415-15646465	AG09319	gingival:	n/a
42	chr17:15644575-15644625	K562	blood:	n/a
43	chr17:15652854-15652904	HIPEpiC	eye:	n/a
44	chr17:15652715-15652765	HNPCEpiC	eye:	n/a
45	chr17:15653096-15653146	AoSMC	blood vessel:	n/a
46	chr17:15652854-15652904	AoSMC	blood vessel:	n/a
47	chr17:15650385-15650435	RPTEC	kidney:	n/a
48	chr17:15652715-15652765	HCM	heart:	n/a
49	chr17:15646415-15646465	GM19239	blood:	n/a
50	chr17:15644575-15644625	AG04449	skin:	fetal

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:15646677..15648283-chr17:15650856..15653224,2	K562	blood:
2	chr17:15646677..15648283-chr17:15650856..15653224,2	K562	blood:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIM16-2	chr17:15652075-15652506	ENSG00000233002.2
2	lnc-TRIM16-6	chr17:15660004-15660081	ucscGeneNc_uc010cow_1
3	lnc-TRIM16-6	chr17:15650705-15650937	NONHSAT145865
4	lnc-TRIM16-7	chr17:15663778-15664123	NONHSAT145868
5	lnc-TRIM16-1	chr17:15666900-15669134	NONHSAT145863
6	lnc-TRIM16-3	chr17:15664928-15665158	ENSG00000233193
7	lnc-TRIM16-6	chr17:15661567-15661699	ucscGeneNc_uc010cow_1
8	lnc-TRIM16-1	chr17:15652017-15652629	NONHSAT145866
9	lnc-TRIM16-6	chr17:15650514-15650937	ucscGeneNc_uc010cow_1
10	lnc-TRIM16-1	chr17:15643410-15648034	NONHSAT145863
11	lnc-TRIM16-1	chr17:15646917-15647105	ENSG00000233002.2
12	lnc-TRIM16-6	chr17:15660004-15660081	NONHSAT145865
13	lnc-TRIM16-1	chr17:15646917-15647113	ENSG00000233002.2
14	lnc-TRIM16-7	chr17:15664746-15664857	NONHSAT145868
15	lnc-TRIM16-3	chr17:15666900-15667083	ENSG00000233193
16	lnc-TRIM16-1	chr17:15649993-15650081	NONHSAT145863
17	lnc-TRIM16-2	chr17:15643942-15644050	ENSG00000233002.2
18	lnc-TRIM16-6	chr17:15661567-15661668	NONHSAT145865

No data

Variant related genes	Relation type
ENSG00000233002	TF binding region
ZSWIM5P1	TF binding region
CDRT15P2	TF binding region
ENSG00000233193	TF binding region
ENSG00000267227	TF binding region
ENSG00000233002	CpG island
ZSWIM5P1	CpG island
CDRT15P2	CpG island
ENSG00000233193	CpG island
ENSG00000267227	CpG island
ENSG00000233002	chromatin interactions
ENSG00000267227	chromatin interactions

Extended variants
information (count: 768 )
Associated
traits (count: 128 )

Variant overlapped rSNPs/rCNVs (count:768 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567547594	chr17:15642564-15642565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs536289081	chr17:15642595-15642596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs555879937	chr17:15642596-15642597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs576137453	chr17:15642639-15642640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs538358108	chr17:15642682-15642683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs558583004	chr17:15642694-15642695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs572321689	chr17:15642706-15642707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs541199679	chr17:15642751-15642752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs181972327	chr17:15642772-15642773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs185988444	chr17:15642800-15642801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs574781139	chr17:15642807-15642808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs543845020	chr17:15642824-15642825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs2529974	chr17:15642835-15642836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs190656269	chr17:15642837-15642838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs2529973	chr17:15642842-15642843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs182535215	chr17:15642848-15642849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs79030109	chr17:15642926-15642927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559855908	chr17:15642945-15642946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs186965210	chr17:15642951-15642952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs547600610	chr17:15642963-15642964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs567608230	chr17:15642987-15642988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs536155488	chr17:15643000-15643001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs79912107	chr17:15643024-15643025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs2529972	chr17:15643029-15643030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs550005179	chr17:15643032-15643033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs569560360	chr17:15643065-15643066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs186507143	chr17:15643084-15643085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs145691264	chr17:15643085-15643086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs2529971	chr17:15643106-15643107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs370035551	chr17:15643107-15643108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs373249290	chr17:15643120-15643121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs558391685	chr17:15643124-15643125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs377641357	chr17:15643132-15643133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571790769	chr17:15643133-15643134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs534927323	chr17:15643138-15643139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs554739802	chr17:15643146-15643147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs574645860	chr17:15643214-15643215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs73978524	chr17:15643217-15643218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs563971141	chr17:15643264-15643265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs577188156	chr17:15643281-15643282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs546155292	chr17:15643305-15643306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs191359208	chr17:15643306-15643307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs143832997	chr17:15643368-15643369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs386795814	chr17:15643377-15643378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs561069300	chr17:15643379-15643380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs529857718	chr17:15643381-15643382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs58354673	chr17:15643382-15643383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs374650936	chr17:15643383-15643384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs202103205	chr17:15643384-15643385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs532040467	chr17:15643385-15643386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:128)

Disease	PMID	Source
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	17603634	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	19435819	CNVD
Non-small cell lung cancer	19010865	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16774939	CNVD
Hepatocellular carcinoma	18803288	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Chordoma	21602918	CNVD
Miller-Dieker syndrome	22283845	CNVD
Non-syndromic sensorineural hearing loss	17457615	CNVD
Cancer	22429812	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Ewing''s sarcoma	21437220	CNVD
Follicular lymphoma	19010834	CNVD
Colorectal cancer	20709793	CNVD
Acute myeloid leukemia	16864856	CNVD
Endometrial cancer	22040021	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Breast cancer	22028636	CNVD
Breast cancer	20837533	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
colon cancer	17210682	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Chronic lymphocytic leukemia	17971485	CNVD
Basal cell lymphoma	17170743	CNVD
Breast cancer	16461572	CNVD
Colorectal cancer	16272173	CNVD
Follicular lymphoma	17170743	CNVD
Human rectal carcinomas	16397240	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Moyamoya disease	22323933	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20724749	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Acute myeloid leukemia	17237825	CNVD
Colorectal cancer	21645411	CNVD
HIV/AIDS	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
HIV/AIDS	17953491	CNVD
HIV/AIDS	20877625	CNVD
Immune disease	21076436	CNVD
Rheumatoid arthritis	17953491	CNVD
Type 1 diabetes	17953491	CNVD
HIV/AIDS	15637236	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Neurofibromatosis	18196300	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Multiple myeloma	16616336	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21509527	CNVD
Pancreatic cancer	21811587	CNVD
Autism	17322880	CNVD
Hereditary neuropathy with liability to pressure palsy	19521722	CNVD
Schizophrenia	19571808	CNVD
Schizophrenia	19955444	CNVD
Charcot-marie-tooth disease	18787571	CNVD
Breast cancer	20409316	CNVD
Autism	18414403	CNVD
Breast cancer	17001317	CNVD
Rhabdomyosarcoma	16790082	CNVD
Myelofibrosis	22110671	CNVD
Peripheral neuropathy	21193943	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	22958593	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	20844748	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Charcot-marie-tooth disease	16463004	CNVD
Osteosarcoma	22292074	CNVD
Charcot	16760730	CNVD
Mental retardation	17901693	CNVD
ovarian endometriomas	16273235	CNVD
Breast cancer	21858162	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17142309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Autism	22102821	CNVD
Gastric cancer	18160780	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:15637400-15647400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr17:15639400-15646400	Weak transcription	Placenta	Placenta
3	chr17:15642000-15644200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr17:15644000-15644200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr17:15644200-15646000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr17:15645200-15646400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr17:15645600-15646000	Flanking Active TSS	Lung	lung
8	chr17:15646000-15647600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr17:15646000-15647600	Weak transcription	Lung	lung
10	chr17:15646400-15648400	Enhancers	Placenta	Placenta
11	chr17:15647400-15648800	Enhancers	Ovary	ovary
12	chr17:15647400-15649000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr17:15647400-15649000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr17:15647600-15647800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr17:15647600-15648000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr17:15647600-15648000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr17:15647600-15648400	Enhancers	Fetal Muscle Leg	muscle
18	chr17:15647600-15648400	Enhancers	Lung	lung
19	chr17:15647800-15649000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr17:15648000-15648400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr17:15648000-15648600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr17:15648000-15648800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr17:15648200-15648800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr17:15648200-15648800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
25	chr17:15648200-15649000	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr17:15648800-15652800	Weak transcription	Ovary	ovary
27	chr17:15651400-15651800	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr17:15651400-15651800	Enhancers	Monocytes-CD14+_RO01746	blood
29	chr17:15652600-15653000	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
30	chr17:15652800-15653000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr17:15652800-15653000	Flanking Active TSS	Ovary	ovary
32	chr17:15652800-15653000	Flanking Active TSS	Psoas Muscle	Psoas
33	chr17:15652800-15653200	Enhancers	Placenta Amnion	Placenta Amnion
34	chr17:15652800-15653400	Active TSS	Right Ventricle	heart
35	chr17:15653000-15654000	Active TSS	Ovary	ovary
36	chr17:15671800-15672000	Enhancers	Fetal Muscle Leg	muscle
37	chr17:15672000-15672800	Weak transcription	Fetal Muscle Leg	muscle
38	chr17:15672000-15673200	Enhancers	Fetal Muscle Trunk	muscle
39	chr17:15672600-15674200	Enhancers	Stomach Smooth Muscle	stomach
40	chr17:15672800-15673000	Bivalent Enhancer	Fetal Stomach	stomach
41	chr17:15672800-15674000	Enhancers	Fetal Muscle Leg	muscle
42	chr17:15672800-15674400	Enhancers	Left Ventricle	heart
43	chr17:15672800-15674800	Enhancers	Fetal Heart	heart
44	chr17:15673200-15673600	Weak transcription	Fetal Muscle Trunk	muscle
45	chr17:15673600-15674000	Enhancers	Fetal Muscle Trunk	muscle
46	chr17:15674000-15674200	Enhancers	Fetal Stomach	stomach

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