Variant report

Variant	nsv888923
Chromosome Location	chr7:103143117-103199719
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	ATF1	chr7:103181075-103181326	K562	blood:	n/a	n/a
2	BACH1	chr7:103169886-103170043	K562	blood:	n/a	n/a
3	BATF	chr7:103188378-103188618	GM12878	blood:	n/a	n/a
4	BATF	chr7:103188327-103188616	GM12878	blood:	n/a	n/a
5	BHLHE40	chr7:103177290-103177312	K562	blood:	n/a	n/a
6	BHLHE40	chr7:103164790-103165165	K562	blood:	n/a	n/a
7	CBX3	chr7:103144961-103145834	K562	blood:	n/a	n/a
8	CBX3	chr7:103146592-103146957	K562	blood:	n/a	n/a
9	CCNT2	chr7:103182534-103182578	K562	blood:	n/a	n/a
10	CEBPB	chr7:103161929-103162195	IMR90	lung:	n/a	chr7:103162067-103162080 chr7:103162067-103162080
11	CEBPB	chr7:103151209-103151430	HepG2	liver:	n/a	chr7:103151301-103151312
12	CEBPB	chr7:103153516-103153722	A549	lung:	n/a	n/a
13	CEBPB	chr7:103179575-103179850	HepG2	liver:	n/a	chr7:103179718-103179729
14	CEBPB	chr7:103151193-103151456	Hela-S3	cervix:	n/a	chr7:103151301-103151312
15	CEBPB	chr7:103151123-103151490	K562	blood:	n/a	chr7:103151135-103151148 chr7:103151301-103151312
16	CEBPB	chr7:103151185-103151461	MCF-7	breast:	n/a	chr7:103151301-103151312
17	CEBPB	chr7:103151176-103151490	K562	blood:	n/a	chr7:103151301-103151312
18	CHD1	chr7:103164668-103165274	IMR90	lung:	n/a	n/a
19	CTCF	chr7:103164880-103165030	GM12801	blood:	n/a	chr7:103164961-103164969 chr7:103164956-103164974 chr7:103164958-103164979
20	CTCF	chr7:103164880-103165030	Hela-S3	cervix:	n/a	chr7:103164961-103164969 chr7:103164956-103164974 chr7:103164958-103164979
21	CTCF	chr7:103164900-103165050	NHLF	lung:	n/a	chr7:103164961-103164969 chr7:103164956-103164974 chr7:103164958-103164979
22	CTCF	chr7:103166545-103166562	MCF-7	breast:	n/a	n/a
23	CTCF	chr7:103164820-103164970	GM12865	blood:	n/a	chr7:103164961-103164969
24	CTCF	chr7:103164711-103165051	A549	lung:	n/a	chr7:103164961-103164969 chr7:103164956-103164974 chr7:103164958-103164979
25	CTCF	chr7:103164894-103165042	GM10248	blood:	n/a	chr7:103164961-103164969 chr7:103164956-103164974 chr7:103164958-103164979
26	CTCF	chr7:103164860-103165010	HFF-Myc	foreskin:	n/a	chr7:103164961-103164969 chr7:103164956-103164974 chr7:103164958-103164979
27	CTCF	chr7:103164780-103164930	GM12866	blood:	n/a	n/a
28	CTCF	chr7:103164880-103165030	HEEpiC	esophagus:	n/a	chr7:103164961-103164969 chr7:103164956-103164974 chr7:103164958-103164979
29	CTCF	chr7:103164880-103165030	AG04450	lung:	n/a	chr7:103164961-103164969 chr7:103164956-103164974 chr7:103164958-103164979
30	CTCF	chr7:103164860-103165010	HPF	lung:	n/a	chr7:103164961-103164969 chr7:103164956-103164974 chr7:103164958-103164979
31	CTCF	chr7:103164811-103165122	HepG2	liver:	n/a	chr7:103164961-103164969 chr7:103164956-103164974 chr7:103164958-103164979
32	CTCF	chr7:103164580-103164730	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr7:103164900-103165050	SK-N-SH_RA	brain:	n/a	chr7:103164961-103164969 chr7:103164956-103164974 chr7:103164958-103164979
34	CTCF	chr7:103164940-103165090	GM12875	blood:	n/a	chr7:103164961-103164969 chr7:103164956-103164974 chr7:103164958-103164979
35	CTCF	chr7:103164880-103165030	SAEC	small airway:	n/a	chr7:103164961-103164969 chr7:103164956-103164974 chr7:103164958-103164979
36	CTCF	chr7:103179533-103179618	MCF-7	breast:	n/a	n/a
37	CTCF	chr7:103164840-103164990	HRPEpiC	eye:	n/a	chr7:103164961-103164969 chr7:103164956-103164974 chr7:103164958-103164979
38	CTCF	chr7:103164860-103165010	RPTEC	kidney:	n/a	chr7:103164961-103164969 chr7:103164956-103164974 chr7:103164958-103164979
39	CTCF	chr7:103164880-103165030	HCFaa	heart:	n/a	chr7:103164961-103164969 chr7:103164956-103164974 chr7:103164958-103164979
40	CTCF	chr7:103164580-103164730	GM12870	blood:	n/a	n/a
41	CTCF	chr7:103164880-103165030	WERI-Rb-1	eye:	n/a	chr7:103164961-103164969 chr7:103164956-103164974 chr7:103164958-103164979
42	CTCF	chr7:103164840-103164990	GM12865	blood:	n/a	chr7:103164961-103164969 chr7:103164956-103164974 chr7:103164958-103164979
43	CTCF	chr7:103164893-103164998	A549	lung:	n/a	chr7:103164961-103164969 chr7:103164956-103164974 chr7:103164958-103164979
44	CTCF	chr7:103164820-103164970	GM12868	blood:	n/a	chr7:103164961-103164969
45	CTCF	chr7:103164940-103165090	HAc	cerebellar:	n/a	chr7:103164961-103164969 chr7:103164956-103164974 chr7:103164958-103164979
46	CTCF	chr7:103164860-103165010	AoAF	blood vessel:	n/a	chr7:103164961-103164969 chr7:103164956-103164974 chr7:103164958-103164979
47	CTCF	chr7:103164900-103165050	HEK293	kidney:	n/a	chr7:103164961-103164969 chr7:103164956-103164974 chr7:103164958-103164979
48	CTCF	chr7:103164880-103165030	HRE	kidney:	n/a	chr7:103164961-103164969 chr7:103164956-103164974 chr7:103164958-103164979
49	CTCF	chr7:103164820-103164970	HVMF	connective:	n/a	chr7:103164961-103164969
50	CTCF	chr7:103164480-103164630	HRPEpiC	eye:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:103169385..103171495-chr7:103172563..103174585,2	K562	blood:
2	chr7:103199365..103201003-chr7:103418048..103420205,2	K562	blood:
3	chr7:103178267..103180295-chr7:103189000..103191734,2	K562	blood:
4	chr7:103157236..103158766-chr7:103162513..103164623,2	MCF-7	breast:
5	chr7:103190662..103192734-chr7:103192820..103195209,2	K562	blood:
6	chr7:103164751..103165375-chr7:103796685..103797398,2	MCF-7	breast:
7	chr7:103160470..103163343-chr7:103165325..103168288,2	MCF-7	breast:
8	chr7:103165602..103166287-chr7:103800636..103801478,2	K562	blood:
9	chr7:103192696..103194335-chr7:103197390..103199163,2	K562	blood:
10	chr7:103155726..103158237-chr7:103158510..103161401,2	MCF-7	breast:
11	chr7:103139301..103141097-chr7:103143967..103145942,2	MCF-7	breast:
12	chr7:103164482..103165037-chr7:103393511..103394116,2	K562	blood:
13	chr7:103138361..103141055-chr7:103143694..103145615,2	K562	blood:
14	chr7:103160470..103163343-chr7:103165325..103168288,2	MCF-7	breast:
15	chr7:103129342..103131885-chr7:103164301..103166214,2	MCF-7	breast:
16	chr7:103162513..103164108-chr7:103188694..103190915,2	MCF-7	breast:
17	chr7:103182952..103185456-chr7:103199000..103201044,2	MCF-7	breast:
18	chr7:103157236..103158766-chr7:103162513..103164623,2	MCF-7	breast:
19	chr7:103184302..103189500-chr7:103191909..103194832,5	K562	blood:
20	chr7:103135205..103136843-chr7:103141167..103143732,2	K562	blood:
21	chr7:103190662..103192734-chr7:103192820..103195209,2	K562	blood:
22	chr7:103153712..103155227-chr7:103156826..103158839,2	K562	blood:
23	chr7:103164527..103165513-chr7:103797019..103797902,4	K562	blood:
24	chr7:103166728..103167430-chr7:103797013..103797864,2	MCF-7	breast:
25	chr7:103156424..103158894-chr7:103835584..103837385,2	K562	blood:
26	chr7:103192696..103194335-chr7:103197390..103199163,2	K562	blood:
27	chr7:103197401..103199581-chr7:103200668..103203292,3	K562	blood:
28	chr7:103164895..103165412-chr7:104559006..104559639,2	K562	blood:
29	chr7:103192591..103194940-chr7:103200480..103202400,2	K562	blood:
30	chr7:103087660..103088653-chr7:103164100..103165409,6	MCF-7	breast:
31	chr7:103153712..103155227-chr7:103156826..103158839,2	K562	blood:
32	chr7:103162513..103164108-chr7:103188694..103190915,2	MCF-7	breast:
33	chr7:103172799..103178070-chr7:103178210..103181701,6	K562	blood:
34	chr7:103155726..103158237-chr7:103158510..103161401,2	MCF-7	breast:
35	chr7:103169385..103171495-chr7:103172563..103174585,2	K562	blood:
36	chr7:103182952..103185456-chr7:103199000..103201044,2	MCF-7	breast:
37	chr7:103184302..103189500-chr7:103191909..103194832,5	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PSMC2-1	chr7:103144851-103144971	ENSG00000234715
2	lnc-PSMC2-1	chr7:103153216-103154454	ENSG00000234715

Variant related genes	Relation type
RELN	TF binding region
ENSG00000189056	chromatin interactions
TRIM59	miRNA target sites
CDK19	miRNA target sites

Extended variants
information (count: 2384 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:2384 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17152191	chr7:103143117-103143118	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs568813128	chr7:103143118-103143119	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs74988109	chr7:103143145-103143146	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs34904354	chr7:103143154-103143155	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs557346700	chr7:103143163-103143164	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs572865956	chr7:103143235-103143236	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs116963021	chr7:103143244-103143245	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs553513259	chr7:103143251-103143252	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs574972067	chr7:103143258-103143259	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs114910094	chr7:103143268-103143269	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs563927127	chr7:103143346-103143347	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs375319118	chr7:103143376-103143377	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs576019453	chr7:103143399-103143400	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs79477580	chr7:103143402-103143403	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs559898276	chr7:103143515-103143516	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs377669512	chr7:103143527-103143528	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs192835206	chr7:103143541-103143542	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs574879897	chr7:103143627-103143628	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs148821179	chr7:103143657-103143658	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs528564288	chr7:103143680-103143681	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs149567032	chr7:103143696-103143697	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs185322698	chr7:103143700-103143701	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs200488546	chr7:103143706-103143707	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs532846105	chr7:103143717-103143718	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs199546320	chr7:103143722-103143723	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs79615780	chr7:103143723-103143724	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs191671732	chr7:103143729-103143730	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs17355678	chr7:103143731-103143732	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs370580315	chr7:103143742-103143743	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs144218164	chr7:103143748-103143749	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs184128313	chr7:103143787-103143788	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs373875667	chr7:103143812-103143813	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs573684562	chr7:103143828-103143829	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs536018562	chr7:103143844-103143845	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs367740692	chr7:103143884-103143885	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs372825647	chr7:103143897-103143898	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs75302567	chr7:103143919-103143920	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs78530360	chr7:103143923-103143924	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546548134	chr7:103143947-103143948	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs2711835	chr7:103144034-103144035	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs17152211	chr7:103144044-103144045	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs540718797	chr7:103144059-103144060	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs561999573	chr7:103144102-103144103	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs139351519	chr7:103144291-103144292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs188089433	chr7:103144302-103144303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs181006752	chr7:103144303-103144304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs578076034	chr7:103144307-103144308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs533038915	chr7:103144335-103144336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs376297308	chr7:103144341-103144342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs202169077	chr7:103144345-103144346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	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
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	19907438	CNVD
Breast cancer	21364760	CNVD
abnormal development	18461090	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	21147910	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:212 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103130800-103155000	Weak transcription	Brain Substantia Nigra	brain
2	chr7:103130800-103163600	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr7:103131200-103145000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr7:103137400-103164400	Weak transcription	Brain Anterior Caudate	brain
5	chr7:103138000-103144200	Strong transcription	HepG2	liver
6	chr7:103142800-103143600	Strong transcription	K562	blood
7	chr7:103143000-103143600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr7:103143600-103144800	Weak transcription	K562	blood
9	chr7:103143600-103153200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr7:103144200-103153000	Weak transcription	HepG2	liver
11	chr7:103144800-103145000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr7:103144800-103145000	Enhancers	K562	blood
13	chr7:103145000-103145200	Active TSS	HUES6 Cell Line	embryonic stem cell
14	chr7:103145000-103145400	Active TSS	ES-I3 Cell Line	embryonic stem cell
15	chr7:103145000-103145400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr7:103145000-103145600	Flanking Active TSS	K562	blood
17	chr7:103145000-103145800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr7:103145200-103145400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
19	chr7:103145200-103145400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr7:103145200-103145600	Active TSS	iPS-15b Cell Line	embryonic stem cell
21	chr7:103145200-103145800	Enhancers	Stomach Mucosa	stomach
22	chr7:103145600-103145800	Enhancers	K562	blood
23	chr7:103153000-103153600	Strong transcription	HepG2	liver
24	chr7:103153200-103153600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr7:103153600-103155600	Weak transcription	HepG2	liver
26	chr7:103155000-103156400	Strong transcription	Brain Substantia Nigra	brain
27	chr7:103155600-103161000	Strong transcription	HepG2	liver
28	chr7:103156000-103162400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr7:103156400-103163800	Weak transcription	Brain Substantia Nigra	brain
30	chr7:103158000-103198600	Weak transcription	Liver	Liver
31	chr7:103158200-103158600	Enhancers	K562	blood
32	chr7:103161000-103168000	Weak transcription	HepG2	liver
33	chr7:103161400-103163400	Weak transcription	Brain Cingulate Gyrus	brain
34	chr7:103162200-103162600	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr7:103162400-103162800	Enhancers	H1 Cell Line	embryonic stem cell
36	chr7:103162400-103162800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr7:103162400-103162800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr7:103162400-103163000	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr7:103162400-103163000	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr7:103162400-103163000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr7:103162400-103163200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr7:103162400-103163200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr7:103162600-103163200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr7:103162800-103168000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr7:103163000-103163800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr7:103163400-103165800	Enhancers	Brain Cingulate Gyrus	brain
47	chr7:103163600-103166000	Enhancers	Brain Inferior Temporal Lobe	brain
48	chr7:103163800-103164200	Enhancers	Brain Hippocampus Middle	brain
49	chr7:103163800-103164400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr7:103163800-103165800	Enhancers	Brain Substantia Nigra	brain

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