Variant report

Variant	nsv1019542
Chromosome Location	chr7:84162664-84200815
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:280)
CpG islands
(count:61)
Chromatin interactive
region (count:12)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:280 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr7:84165333-84165902	A549	lung:	n/a	n/a
2	ATF3	chr7:84165356-84165961	A549	lung:	n/a	n/a
3	BCL11A	chr7:84177692-84177958	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr7:84165334-84165953	A549	lung:	n/a	n/a
5	BCL3	chr7:84165165-84166072	A549	lung:	n/a	n/a
6	CEBPB	chr7:84165263-84166264	A549	lung:	n/a	n/a
7	CEBPB	chr7:84178753-84179115	Hela-S3	cervix:	n/a	chr7:84178925-84178936 chr7:84178858-84178870 chr7:84178857-84178870
8	CEBPB	chr7:84178758-84179104	HepG2	liver:	n/a	chr7:84178925-84178936 chr7:84178858-84178870 chr7:84178857-84178870
9	CEBPB	chr7:84178760-84179074	H1-hESC	embryonic stem cell:	n/a	chr7:84178925-84178936 chr7:84178858-84178870 chr7:84178857-84178870
10	CEBPB	chr7:84178769-84179117	A549	lung:	n/a	chr7:84178925-84178936 chr7:84178858-84178870 chr7:84178857-84178870
11	CEBPB	chr7:84177667-84178429	ECC-1	luminal epithelium:	n/a	chr7:84178224-84178237 chr7:84178225-84178236
12	CEBPB	chr7:84177668-84178447	ECC-1	luminal epithelium:	n/a	chr7:84178224-84178237 chr7:84178225-84178236
13	CEBPB	chr7:84165421-84166199	A549	lung:	n/a	n/a
14	CEBPB	chr7:84178114-84178352	K562	blood:	n/a	chr7:84178224-84178237 chr7:84178225-84178236
15	CEBPB	chr7:84178757-84179118	ECC-1	luminal epithelium:	n/a	chr7:84178925-84178936 chr7:84178858-84178870 chr7:84178857-84178870
16	CEBPB	chr7:84165297-84166222	MCF-7	breast:	n/a	n/a
17	CEBPB	chr7:84178130-84178390	HepG2	liver:	n/a	chr7:84178224-84178237 chr7:84178225-84178236
18	CEBPB	chr7:84178056-84178365	A549	lung:	n/a	chr7:84178224-84178237 chr7:84178225-84178236
19	CEBPB	chr7:84178732-84179117	ECC-1	luminal epithelium:	n/a	chr7:84178925-84178936 chr7:84178858-84178870 chr7:84178857-84178870
20	CEBPB	chr7:84178770-84179209	A549	lung:	n/a	chr7:84178925-84178936 chr7:84178858-84178870 chr7:84178857-84178870
21	CEBPB	chr7:84178069-84178389	IMR90	lung:	n/a	chr7:84178224-84178237 chr7:84178225-84178236
22	CEBPB	chr7:84178229-84178319	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr7:84165419-84166142	A549	lung:	n/a	n/a
24	CEBPB	chr7:84178742-84179124	IMR90	lung:	n/a	chr7:84178925-84178936 chr7:84178858-84178870 chr7:84178857-84178870
25	CEBPB	chr7:84178751-84179115	K562	blood:	n/a	chr7:84178925-84178936 chr7:84178858-84178870 chr7:84178857-84178870
26	CEBPB	chr7:84178071-84178396	Hela-S3	cervix:	n/a	chr7:84178224-84178237 chr7:84178225-84178236
27	CHD2	chr7:84177738-84177801	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr7:84170960-84171110	HRE	kidney:	n/a	n/a
29	CTCF	chr7:84171180-84171330	GM12870	blood:	n/a	n/a
30	CTCF	chr7:84178320-84178470	HEK293	kidney:	n/a	n/a
31	CTCF	chr7:84171140-84171290	HA-sp	spinal cord:	n/a	n/a
32	CTCF	chr7:84171140-84171290	GM12869	blood:	n/a	n/a
33	CTCF	chr7:84171140-84171290	RPTEC	kidney:	n/a	n/a
34	CTCF	chr7:84170980-84171250	GM12873	blood:	n/a	n/a
35	CTCF	chr7:84171140-84171290	GM12866	blood:	n/a	n/a
36	CTCF	chr7:84171180-84171330	AG10803	skin:	n/a	n/a
37	CTCF	chr7:84171100-84171250	GM12874	blood:	n/a	n/a
38	CTCF	chr7:84171120-84171270	HepG2	liver:	n/a	n/a
39	CTCF	chr7:84171180-84171330	HEEpiC	esophagus:	n/a	n/a
40	CTCF	chr7:84175832-84175966	HepG2	liver:	n/a	n/a
41	CTCF	chr7:84171140-84171290	HEK293	kidney:	n/a	n/a
42	CTCF	chr7:84171140-84171290	HMEC	breast:	n/a	n/a
43	CTCF	chr7:84175800-84175950	HepG2	liver:	n/a	n/a
44	CTCF	chr7:84171120-84171270	AG04450	lung:	n/a	n/a
45	CTCF	chr7:84171180-84171330	GM12878	blood:	n/a	n/a
46	CTCF	chr7:84171240-84171390	HVMF	connective:	n/a	n/a
47	CTCF	chr7:84171140-84171290	MCF-7	breast:	n/a	n/a
48	CTCF	chr7:84171240-84171390	BE2_C	brain:	n/a	n/a
49	CTCF	chr7:84171100-84171250	GM12865	blood:	n/a	n/a
50	CTCF	chr7:84171180-84171330	AoAF	blood vessel:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:84177905-84177955	SK-N-SH_RA	brain:	n/a
2	chr7:84177905-84177955	HMEC	breast:	n/a
3	chr7:84177905-84177955	HRPEpiC	eye:	n/a
4	chr7:84177905-84177955	ovcar-3	ovarian:	n/a
5	chr7:84177905-84177955	NHBE	bronchial:	n/a
6	chr7:84177905-84177955	NT2-D1	testis:	n/a
7	chr7:84177905-84177955	SK-N-SH	brain:	n/a
8	chr7:84177905-84177955	ProgFib	skin:	n/a
9	chr7:84177905-84177955	SAEC	small airway:	n/a
10	chr7:84177905-84177955	BE2_C	brain:	n/a
11	chr7:84177905-84177955	HRE	kidney:	n/a
12	chr7:84177905-84177955	GM06990	blood:	n/a
13	chr7:84177905-84177955	AG09319	gingival:	n/a
14	chr7:84177905-84177955	Caco-2	colon:	n/a
15	chr7:84177905-84177955	U87	brain:	n/a
16	chr7:84177905-84177955	HEEpiC	esophagus:	n/a
17	chr7:84177905-84177955	AG04449	skin:	fetal
18	chr7:84177905-84177955	HNPCEpiC	eye:	n/a
19	chr7:84177905-84177955	NHDF-neo	bronchial:	n/a
20	chr7:84177905-84177955	GM12892	blood:	n/a
21	chr7:84177905-84177955	SK-N-MC	brain:	n/a
22	chr7:84177905-84177955	PrEC	prostate:	n/a
23	chr7:84177905-84177955	LNCaP	prostate:	n/a
24	chr7:84177905-84177955	HRCEpiC	kidney:	n/a
25	chr7:84177905-84177955	Hepatocyte	liver:	n/a
26	chr7:84177905-84177955	HUVEC	blood vessel:	n/a
27	chr7:84177905-84177955	A549	lung:	n/a
28	chr7:84177905-84177955	Hela-S3	cervix:	n/a
29	chr7:84177905-84177955	ECC-1	luminal epithelium:	n/a
30	chr7:84177905-84177955	AG04450	lung:	fetal
31	chr7:84177905-84177955	HCPEpiC	choroid plexus:	n/a
32	chr7:84177905-84177955	HL-60	blood:	n/a
33	chr7:84177905-84177955	MCF-7	breast:	n/a
34	chr7:84177905-84177955	HIPEpiC	eye:	n/a
35	chr7:84177905-84177955	PANC-1	pancreas:	n/a
36	chr7:84177905-84177955	AG09309	skin:	n/a
37	chr7:84177905-84177955	NH-A	brain:	n/a
38	chr7:84177905-84177955	AG10803	skin:	n/a
39	chr7:84177905-84177955	GM12891	blood:	n/a
40	chr7:84177905-84177955	SKMC	muscle:	n/a
41	chr7:84177905-84177955	RPTEC	kidney:	n/a
42	chr7:84177905-84177955	HCM	heart:	n/a
43	chr7:84177905-84177955	GM19239	blood:	n/a
44	chr7:84177905-84177955	H1-hESC	embryonic stem cell:	embryo
45	chr7:84177905-84177955	MCF10A-Er-Src	breast:	n/a
46	chr7:84177905-84177955	BJ	skin:	n/a
47	chr7:84177905-84177955	HPAEpiC	pulmonary alveolar:	n/a
48	chr7:84177905-84177955	HCT-116	colon:	n/a
49	chr7:84177905-84177955	CMK	blood:	n/a
50	chr7:84177905-84177955	AoSMC	blood vessel:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:84165149..84165684-chr7:84582450..84583007,2	MCF-7	breast:
2	chr7:84165408..84168410-chr7:84171249..84173353,3	K562	blood:
3	chr7:84165204..84166004-chr7:84499385..84500020,2	MCF-7	breast:
4	chr1:149857245..149858849-chr7:84173495..84175226,2	MCF-7	breast:
5	chr7:84170149..84172689-chr7:84175115..84178110,2	MCF-7	breast:
6	chr7:84165144..84166088-chr7:84499191..84500054,5	MCF-7	breast:
7	chr7:84172414..84174090-chr7:84421942..84424878,2	K562	blood:
8	chr7:84165408..84168410-chr7:84171249..84173353,3	K562	blood:
9	chr7:83904428..83905120-chr7:84165177..84165677,2	MCF-7	breast:
10	chr7:84170149..84172689-chr7:84175115..84178110,2	MCF-7	breast:
11	chr7:84165588..84166207-chr7:84499370..84499987,2	MCF-7	breast:
12	chr7:84165149..84166023-chr7:84582151..84583096,5	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GRM3-2	chr7:84200294-84200423	NONHSAT121790
2	lnc-GRM3-2	chr7:84178463-84178569	XLOC_006159
3	lnc-GRM3-2	chr7:84200295-84204159	XLOC_006159
4	lnc-GRM3-2	chr7:84178522-84178569	XLOC_006159
5	lnc-GRM3-2	chr7:84178463-84178569	NR_110080
6	lnc-GRM3-2	chr7:84200295-84200423	NR_110080
7	lnc-GRM3-2	chr7:84178521-84178569	NONHSAT121790
8	lnc-GRM3-2	chr7:84200295-84200423	XLOC_006159

No data

Variant related genes	Relation type
ENSG00000235139	TF binding region
RPL7P30	TF binding region
ENSG00000235139	CpG island
RPL7P30	CpG island
ENSG00000184678	chromatin interactions
ENSG00000184260	chromatin interactions
ARFIP1	miRNA target sites
ARFGEF1	miRNA target sites

Extended variants
information (count: 969 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:969 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73712923	chr7:84162739-84162740	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs187795263	chr7:84162771-84162772	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs17159109	chr7:84162817-84162818	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs551536068	chr7:84162837-84162838	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs569990907	chr7:84162870-84162871	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs537336578	chr7:84162898-84162899	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs555661597	chr7:84162902-84162903	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs574089394	chr7:84162943-84162944	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs62472048	chr7:84163028-84163029	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs555255756	chr7:84163043-84163044	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs191106423	chr7:84163082-84163083	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs567625319	chr7:84163084-84163085	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs545300900	chr7:84163088-84163089	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs145718651	chr7:84163130-84163131	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs575574442	chr7:84163137-84163138	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs11980222	chr7:84163152-84163153	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs561198415	chr7:84163200-84163201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs17159110	chr7:84163217-84163218	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs76442744	chr7:84163242-84163243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs2023990	chr7:84163284-84163285	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs559214016	chr7:84163288-84163289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs138672565	chr7:84163306-84163307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs577701824	chr7:84163326-84163327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs142734182	chr7:84163343-84163344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs569854365	chr7:84163378-84163379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs147385009	chr7:84163444-84163445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs139109561	chr7:84163471-84163472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs2023991	chr7:84163502-84163503	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs534745918	chr7:84163507-84163508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs537072057	chr7:84163522-84163523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs149398985	chr7:84163544-84163545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs571696987	chr7:84163545-84163546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs73712927	chr7:84163554-84163555	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs576850428	chr7:84163561-84163562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs575435042	chr7:84163587-84163588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs542784606	chr7:84163618-84163619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs73712928	chr7:84163655-84163656	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs573992022	chr7:84163684-84163685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs573182143	chr7:84163694-84163695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs371444857	chr7:84163797-84163798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs559296909	chr7:84163803-84163804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs77226756	chr7:84163882-84163883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs545092539	chr7:84163901-84163902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs563345928	chr7:84163905-84163906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs530744917	chr7:84163915-84163916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs144806581	chr7:84164002-84164003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs62472049	chr7:84164072-84164073	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs528384195	chr7:84164082-84164083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs546720254	chr7:84164084-84164085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs148584552	chr7:84164099-84164100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Biliary cancer	19435499	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Neurodevelopmental disorder	22521361	CNVD
Metanephric adenoma	20802469	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Williams-beuren syndrome	16826523	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	19318497	CNVD
Multiple myeloma	16616336	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	20858243	CNVD
Renal cell carcinoma	18194544	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:84159400-84165000	Weak transcription	Colon Smooth Muscle	Colon
2	chr7:84160000-84165400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr7:84160800-84165200	Weak transcription	Rectal Smooth Muscle	rectum
4	chr7:84160800-84165200	Weak transcription	Hela-S3	cervix
5	chr7:84161000-84162800	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr7:84161000-84163000	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr7:84161000-84163200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr7:84161200-84162800	Enhancers	NHDF-Ad	bronchial
9	chr7:84161800-84163000	Active TSS	Fetal Kidney	kidney
10	chr7:84161800-84164800	Weak transcription	Fetal Intestine Large	intestine
11	chr7:84161800-84165400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr7:84161800-84165400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr7:84162000-84164800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr7:84162000-84164800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr7:84162200-84162800	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr7:84162400-84164200	Weak transcription	A549	lung
17	chr7:84162400-84164600	Weak transcription	Fetal Intestine Small	intestine
18	chr7:84162600-84163000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr7:84162600-84163000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr7:84162800-84163000	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr7:84162800-84165400	Weak transcription	NHDF-Ad	bronchial
22	chr7:84163000-84165400	Weak transcription	Fetal Kidney	kidney
23	chr7:84163200-84164800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr7:84164200-84164800	Enhancers	A549	lung
25	chr7:84164600-84166200	Enhancers	Fetal Intestine Small	intestine
26	chr7:84164800-84165800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr7:84164800-84165800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr7:84164800-84166200	Enhancers	Fetal Intestine Large	intestine
29	chr7:84164800-84166400	Flanking Active TSS	A549	lung
30	chr7:84164800-84166800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr7:84165000-84165800	Enhancers	Stomach Smooth Muscle	stomach
32	chr7:84165000-84166200	Enhancers	Colon Smooth Muscle	Colon
33	chr7:84165200-84166000	Enhancers	Rectal Smooth Muscle	rectum
34	chr7:84165200-84166200	Enhancers	Hela-S3	cervix
35	chr7:84165400-84165800	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr7:84165400-84165800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr7:84165400-84166000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr7:84165400-84166000	Enhancers	NHDF-Ad	bronchial
39	chr7:84165400-84166200	Enhancers	Fetal Kidney	kidney
40	chr7:84166000-84168800	Weak transcription	Rectal Smooth Muscle	rectum
41	chr7:84166200-84168800	Weak transcription	Colon Smooth Muscle	Colon
42	chr7:84166400-84169200	Enhancers	A549	lung
43	chr7:84168800-84169600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr7:84168800-84169600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr7:84168800-84169600	Enhancers	Colon Smooth Muscle	Colon
46	chr7:84168800-84169600	Enhancers	Rectal Smooth Muscle	rectum
47	chr7:84175800-84176000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr7:84176000-84181800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr7:84176800-84177000	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr7:84176800-84179000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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