Variant report

Variant	nsv429752
Chromosome Location	chr7:50607353-50620030
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:40)
CpG islands
(count:244)
Chromatin interactive
region (count:4)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:40 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr7:50612762-50612930	HepG2	liver:	n/a	n/a
2	CEBPB	chr7:50615131-50615309	IMR90	lung:	n/a	chr7:50615249-50615260
3	CEBPB	chr7:50615095-50615402	HepG2	liver:	n/a	chr7:50615249-50615260
4	CEBPB	chr7:50612799-50612953	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr7:50612690-50613026	HepG2	liver:	n/a	n/a
6	CTCF	chr7:50614540-50614690	GM12873	blood:	n/a	n/a
7	FOXA1	chr7:50619798-50620204	HepG2	liver:	n/a	chr7:50619939-50619954
8	FOXA1	chr7:50612621-50613005	HepG2	liver:	n/a	n/a
9	FOXA1	chr7:50612594-50613042	HepG2	liver:	n/a	n/a
10	FOXA1	chr7:50619818-50620146	HepG2	liver:	n/a	chr7:50619939-50619954
11	FOXA1	chr7:50619705-50620211	HepG2	liver:	n/a	chr7:50619939-50619954
12	FOXA1	chr7:50612649-50613088	HepG2	liver:	n/a	n/a
13	FOXA1	chr7:50619755-50620251	HepG2	liver:	n/a	chr7:50619939-50619954
14	FOXA1	chr7:50612696-50612980	T-47D	breast:	n/a	n/a
15	FOXA1	chr7:50612644-50613028	HepG2	liver:	n/a	n/a
16	FOXA1	chr7:50612720-50612968	T-47D	breast:	n/a	n/a
17	FOXA2	chr7:50612677-50612978	HepG2	liver:	n/a	n/a
18	FOXA2	chr7:50619757-50620146	HepG2	liver:	n/a	n/a
19	FOXA2	chr7:50612440-50613061	HepG2	liver:	n/a	n/a
20	GATA3	chr7:50614370-50614636	T-47D	breast:	n/a	n/a
21	HDAC2	chr7:50619847-50620161	HepG2	liver:	n/a	n/a
22	JUN	chr7:50616925-50617069	K562	blood:	n/a	n/a
23	MAFK	chr7:50613592-50613653	HepG2	liver:	n/a	n/a
24	MAFK	chr7:50613585-50613664	HepG2	liver:	n/a	n/a
25	MAFK	chr7:50614631-50614762	HepG2	liver:	n/a	n/a
26	MAFK	chr7:50619562-50619653	Hela-S3	cervix:	n/a	n/a
27	MAX	chr7:50609007-50609054	NB4	blood:	n/a	chr7:50609016-50609026 chr7:50609018-50609027 chr7:50609016-50609029 chr7:50609016-50609029 chr7:50609018-50609028 chr7:50609017-50609028 chr7:50609016-50609031 chr7:50609017-50609028
28	MAX	chr7:50608870-50609123	K562	blood:	n/a	chr7:50609016-50609026 chr7:50609018-50609027 chr7:50609016-50609029 chr7:50609016-50609029 chr7:50609018-50609028 chr7:50609017-50609028 chr7:50609016-50609031 chr7:50609017-50609028
29	NFYB	chr7:50614060-50614347	K562	blood:	n/a	n/a
30	NRF1	chr7:50609543-50609626	H1-hESC	embryonic stem cell:	n/a	n/a
31	POLR2A	chr7:50607645-50607774	MCF-7	breast:	n/a	n/a
32	POLR2A	chr7:50619822-50620258	H1-neurons	neurons:	n/a	n/a
33	POLR2A	chr7:50619879-50620300	H1-neurons	neurons:	n/a	n/a
34	POLR2A	chr7:50614148-50614312	MCF10A-Er-Src	breast:	n/a	n/a
35	POLR2A	chr7:50608894-50608932	MCF-7	breast:	n/a	n/a
36	POLR2A	chr7:50608967-50608975	MCF-7	breast:	n/a	n/a
37	POLR2A	chr7:50612925-50613011	MCF10A-Er-Src	breast:	n/a	n/a
38	REST	chr7:50619955-50620260	PFSK-1	brain:	n/a	n/a
39	SPI1	chr7:50613965-50614335	HL-60	blood:	n/a	n/a
40	ZNF263	chr7:50608671-50609089	HEK293-T-REx	kidney:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:50611949-50611999	HIPEpiC	eye:	n/a
2	chr7:50611949-50611999	NHDF-neo	bronchial:	n/a
3	chr7:50611949-50611999	AG10803	skin:	n/a
4	chr7:50611884-50611934	HRE	kidney:	n/a
5	chr7:50611884-50611934	AG10803	skin:	n/a
6	chr7:50612853-50612903	Jurkat	blood:	n/a
7	chr7:50611949-50611999	K562	blood:	n/a
8	chr7:50611949-50611999	NB4	blood:	n/a
9	chr7:50612053-50612103	HEEpiC	esophagus:	n/a
10	chr7:50611884-50611934	HIPEpiC	eye:	n/a
11	chr7:50611884-50611934	SK-N-SH	brain:	n/a
12	chr7:50612053-50612103	HPAEpiC	pulmonary alveolar:	n/a
13	chr7:50611949-50611999	SK-N-MC	brain:	n/a
14	chr7:50611949-50611999	AoSMC	blood vessel:	n/a
15	chr7:50612853-50612903	RPTEC	kidney:	n/a
16	chr7:50611949-50611999	LNCaP	prostate:	n/a
17	chr7:50612053-50612103	HepG2	liver:	n/a
18	chr7:50611884-50611934	U87	brain:	n/a
19	chr7:50612853-50612903	HEEpiC	esophagus:	n/a
20	chr7:50612053-50612103	HMEC	breast:	n/a
21	chr7:50611884-50611934	ovcar-3	ovarian:	n/a
22	chr7:50612853-50612903	HIPEpiC	eye:	n/a
23	chr7:50612853-50612903	HepG2	liver:	n/a
24	chr7:50611949-50611999	Hepatocyte	liver:	n/a
25	chr7:50612053-50612103	AG09319	gingival:	n/a
26	chr7:50612053-50612103	MCF10A-Er-Src	breast:	n/a
27	chr7:50612053-50612103	AG10803	skin:	n/a
28	chr7:50611884-50611934	HL-60	blood:	n/a
29	chr7:50611884-50611934	GM12878	blood:	n/a
30	chr7:50611949-50611999	HAEpiC	amniotic membrane:	n/a
31	chr7:50612053-50612103	PrEC	prostate:	n/a
32	chr7:50611884-50611934	HEK293	kidney:	embryo
33	chr7:50611884-50611934	AoSMC	blood vessel:	n/a
34	chr7:50612853-50612903	AG10803	skin:	n/a
35	chr7:50611949-50611999	HCT-116	colon:	n/a
36	chr7:50611884-50611934	NB4	blood:	n/a
37	chr7:50611949-50611999	GM06990	blood:	n/a
38	chr7:50612853-50612903	SK-N-MC	brain:	n/a
39	chr7:50612853-50612903	AG09319	gingival:	n/a
40	chr7:50612053-50612103	GM19239	blood:	n/a
41	chr7:50611884-50611934	LNCaP	prostate:	n/a
42	chr7:50612053-50612103	HUVEC	blood vessel:	n/a
43	chr7:50612853-50612903	Hela-S3	cervix:	n/a
44	chr7:50612853-50612903	LNCaP	prostate:	n/a
45	chr7:50611949-50611999	HCPEpiC	choroid plexus:	n/a
46	chr7:50612053-50612103	HRCEpiC	kidney:	n/a
47	chr7:50611884-50611934	Caco-2	colon:	n/a
48	chr7:50611949-50611999	GM12892	blood:	n/a
49	chr7:50611884-50611934	HCPEpiC	choroid plexus:	n/a
50	chr7:50611949-50611999	GM19239	blood:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:50609777..50612702-chr7:50615393..50617097,3	K562	blood:
2	chr7:50601800..50604303-chr7:50605834..50607689,2	K562	blood:
3	chr7:50605928..50607774-chr7:50609469..50611799,3	MCF-7	breast:
4	chr7:50605928..50607774-chr7:50609469..50611799,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IKZF1-1	chr7:50607529-50607843	ENSG00000226122.1
2	lnc-IKZF1-1	chr7:50609044-50609107	ENSG00000226122.1
3	lnc-IKZF1-1	chr7:50609943-50611161	ENSG00000226122.1

No data

Variant related genes	Relation type
DDC	TF binding region
DDC	CpG island
ENSG00000132437	chromatin interactions

Extended variants
information (count: 522 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:522 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11575309	chr7:50607353-50607354	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs11575308	chr7:50607368-50607369	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs998850	chr7:50607388-50607389	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs11575306	chr7:50607392-50607393	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs117160167	chr7:50607433-50607434	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs11575305	chr7:50607480-50607481	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs11575304	chr7:50607482-50607483	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs11575303	chr7:50607505-50607506	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs114074352	chr7:50607515-50607516	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs536886627	chr7:50607516-50607517	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs556557785	chr7:50607530-50607531	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs576719895	chr7:50607543-50607544	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs545013377	chr7:50607561-50607562	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs369615710	chr7:50607562-50607563	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs550484577	chr7:50607585-50607586	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs201345722	chr7:50607592-50607593	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs201015793	chr7:50607599-50607600	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs369907099	chr7:50607603-50607604	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
19	rs192659401	chr7:50607619-50607620	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs137853207	chr7:50607624-50607625	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs200339845	chr7:50607629-50607630	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs561069897	chr7:50607655-50607656	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs137853211	chr7:50607656-50607657	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs200437940	chr7:50607667-50607668	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs367959876	chr7:50607673-50607674	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs11575302	chr7:50607694-50607695	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs140276979	chr7:50607696-50607697	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs61731774	chr7:50607721-50607722	Weak transcription Enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs199573720	chr7:50607729-50607730	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
30	rs184592700	chr7:50607753-50607754	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
31	rs145847787	chr7:50607785-50607786	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs571329045	chr7:50607803-50607804	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs527744977	chr7:50607817-50607818	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs547558349	chr7:50607826-50607827	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs567777134	chr7:50607839-50607840	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs138687055	chr7:50607889-50607890	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs200179830	chr7:50607993-50607994	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566005665	chr7:50608040-50608041	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs375016441	chr7:50608042-50608043	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs539346729	chr7:50608088-50608089	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs558561822	chr7:50608100-50608101	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs572053147	chr7:50608121-50608122	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs541053239	chr7:50608124-50608125	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs557844519	chr7:50608133-50608134	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs201255362	chr7:50608189-50608190	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs554363359	chr7:50608190-50608191	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs201412703	chr7:50608192-50608193	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs149353795	chr7:50608193-50608194	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs35299591	chr7:50608194-50608195	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs111598843	chr7:50608197-50608198	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:120)

Disease	PMID	Source
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Biliary cancer	19435499	CNVD
Wilms tumour	21544195	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	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
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Autism	22495311	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	17237825	CNVD
Gastric cancer	24379144	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Esophageal cancer	21851588	CNVD
Non-small cell lung cancer	17643093	CNVD
Ovarian cancer	18182111	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17369134	CNVD
Barrett''s esophagus	18559552	CNVD
head and neck squamous cell carcinoma	16943533	CNVD
Anaplastic thyroid cancer	17079354	CNVD
Basal-like breast cancer	17875215	CNVD
Colorectal cancer	16882699	CNVD
Colorectal cancer	18794099	CNVD
Gastrointestinal stromal cancer	17643098	CNVD
Lung cancer	18381415	CNVD
Metastatic colorectal cancer	17664472	CNVD
Non-small cell lung cancer	19255323	CNVD
Non-small cell lung cancer	17673923	CNVD
Non-small cell lung cancer	17975165	CNVD
Non-small cell lung cancer	19622585	CNVD
Ovarian cancer	16607561	CNVD
Squamous cell cancer	19670535	CNVD
head and neck squamous cell carcinoma	16818711	CNVD
small cell lung cancer	18829487	CNVD
Breast cancer	17661082	CNVD
Adenocarcinoma	19260752	CNVD
Esophageal cancer	16575012	CNVD
Lung adenocarcinoma	19138956	CNVD
Lung adenocarcinoma	18379350	CNVD
Lung adenocarcinoma	18258923	CNVD
Lung cancer	19138956	CNVD
Lung cancer	18379350	CNVD
Lung cancer	18258923	CNVD
Non-small cell lung cancer	18304967	CNVD
Non-small cell lung cancer	19451690	CNVD
Non-small cell lung cancer	19260752	CNVD
Non-small cell lung cancer	17079354	CNVD
Non-small cell lung cancer	18559607	CNVD
Rectal cancer	19506820	CNVD
Triple-negative breast cancer	18950515	CNVD
head and neck squamous cell carcinoma	18813952	CNVD
Non-small cell lung cancer	17504988	CNVD
Non-small cell lung cancer	16943533	CNVD
Non-small cell lung cancer	18509184	CNVD
head and neck squamous cell carcinoma	17538160	CNVD
Colorectal cancer	19712476	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Lung cancer	19671679	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
small cell lung cancer	20016488	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Hirschsprung''s Disease	21712996	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:50565200-50609000	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr7:50600200-50612600	Weak transcription	Small Intestine	intestine
3	chr7:50600600-50619400	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr7:50601600-50631400	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr7:50602600-50618200	Weak transcription	Pancreas	Pancrea
6	chr7:50602800-50609600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr7:50602800-50610200	Weak transcription	Colonic Mucosa	Colon
8	chr7:50602800-50613800	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr7:50603600-50613000	Strong transcription	Duodenum Mucosa	Duodenum
10	chr7:50604000-50612000	Strong transcription	Fetal Intestine Large	intestine
11	chr7:50604400-50612000	Strong transcription	HepG2	liver
12	chr7:50604600-50609600	Weak transcription	Liver	Liver
13	chr7:50604600-50612400	Strong transcription	Fetal Intestine Small	intestine
14	chr7:50606400-50608000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr7:50607000-50612000	Weak transcription	Fetal Stomach	stomach
16	chr7:50608000-50608400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr7:50608400-50608600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr7:50608600-50610000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr7:50609000-50611800	Strong transcription	Rectal Mucosa Donor 29	rectum
20	chr7:50609600-50609800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr7:50609600-50611600	Strong transcription	Liver	Liver
22	chr7:50609800-50610200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr7:50610000-50610400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr7:50610000-50611200	Weak transcription	Stomach Mucosa	stomach
25	chr7:50610200-50610600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr7:50610200-50611000	Strong transcription	Colonic Mucosa	Colon
27	chr7:50610200-50611000	Enhancers	Placenta	Placenta
28	chr7:50610600-50611000	Weak transcription	Spleen	Spleen
29	chr7:50611000-50631800	Weak transcription	Colonic Mucosa	Colon
30	chr7:50611600-50623800	Weak transcription	Liver	Liver
31	chr7:50611800-50614200	Weak transcription	Rectal Mucosa Donor 29	rectum
32	chr7:50612000-50612600	Weak transcription	HepG2	liver
33	chr7:50612000-50619600	Weak transcription	Fetal Intestine Large	intestine
34	chr7:50612400-50617600	Weak transcription	Fetal Intestine Small	intestine
35	chr7:50612600-50613000	Enhancers	HepG2	liver
36	chr7:50613000-50614400	Weak transcription	HepG2	liver
37	chr7:50613000-50621600	Weak transcription	Duodenum Mucosa	Duodenum
38	chr7:50614000-50614400	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr7:50614000-50614400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr7:50614400-50614800	Enhancers	HepG2	liver
41	chr7:50614800-50619400	Weak transcription	HepG2	liver
42	chr7:50617600-50619400	Strong transcription	Fetal Intestine Small	intestine
43	chr7:50617800-50618000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
44	chr7:50618200-50618400	Enhancers	Fetal Lung	lung
45	chr7:50618200-50618600	Enhancers	Pancreas	Pancrea
46	chr7:50618600-50620000	Weak transcription	Pancreas	Pancrea
47	chr7:50619400-50620600	Enhancers	Pancreatic Islets	Pancreatic Islet
48	chr7:50619400-50624400	Genic enhancers	Fetal Intestine Small	intestine
49	chr7:50619400-50628200	Enhancers	HepG2	liver
50	chr7:50619600-50620600	Enhancers	Stomach Mucosa	stomach

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