Variant report

Variant	nsv608466
Chromosome Location	chr7:137356651-137404781
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	ARID3A	chr7:137380646-137381136	HepG2	liver:	n/a	n/a
2	ATF2	chr7:137402631-137403096	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr7:137402686-137402952	K562	blood:	n/a	n/a
4	BACH1	chr7:137402628-137402982	H1-hESC	embryonic stem cell:	n/a	chr7:137402800-137402814
5	BATF	chr7:137402665-137402933	GM12878	blood:	n/a	chr7:137402800-137402810 chr7:137402799-137402810
6	BHLHE40	chr7:137380718-137381057	HepG2	liver:	n/a	n/a
7	BHLHE40	chr7:137379871-137380030	GM12878	blood:	n/a	n/a
8	BHLHE40	chr7:137380676-137381268	HepG2	liver:	n/a	n/a
9	BHLHE40	chr7:137379092-137379535	GM12878	blood:	n/a	n/a
10	CEBPB	chr7:137361723-137361870	K562	blood:	n/a	n/a
11	CEBPB	chr7:137400019-137400231	IMR90	lung:	n/a	n/a
12	CEBPB	chr7:137376335-137376647	A549	lung:	n/a	chr7:137376410-137376423 chr7:137376479-137376490 chr7:137376478-137376489 chr7:137376480-137376489 chr7:137376478-137376491
13	CEBPB	chr7:137366916-137367281	HepG2	liver:	n/a	chr7:137367094-137367105
14	CEBPB	chr7:137367000-137367219	H1-hESC	embryonic stem cell:	n/a	chr7:137367094-137367105
15	CEBPB	chr7:137366929-137367275	K562	blood:	n/a	chr7:137367094-137367105
16	CEBPB	chr7:137366958-137367187	A549	lung:	n/a	chr7:137367094-137367105
17	CEBPB	chr7:137366924-137367269	A549	lung:	n/a	chr7:137367094-137367105
18	CEBPB	chr7:137376343-137376608	K562	blood:	n/a	chr7:137376410-137376423 chr7:137376479-137376490 chr7:137376478-137376489 chr7:137376480-137376489 chr7:137376478-137376491
19	CEBPB	chr7:137366629-137367681	IMR90	lung:	n/a	chr7:137367094-137367105
20	CEBPB	chr7:137366972-137367259	MCF-7	breast:	n/a	chr7:137367094-137367105
21	CEBPB	chr7:137366847-137367341	A549	lung:	n/a	chr7:137367094-137367105
22	CEBPB	chr7:137376308-137376664	IMR90	lung:	n/a	chr7:137376410-137376423 chr7:137376479-137376490 chr7:137376478-137376489 chr7:137376480-137376489 chr7:137376478-137376491
23	CEBPB	chr7:137376353-137376553	Hela-S3	cervix:	n/a	chr7:137376410-137376423 chr7:137376479-137376490 chr7:137376478-137376489 chr7:137376480-137376489 chr7:137376478-137376491
24	CEBPB	chr7:137402537-137403091	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr7:137366904-137367298	Hela-S3	cervix:	n/a	chr7:137367094-137367105
26	CEBPB	chr7:137356764-137356797	HepG2	liver:	n/a	n/a
27	CEBPB	chr7:137401248-137401492	IMR90	lung:	n/a	n/a
28	CEBPB	chr7:137376305-137376644	HepG2	liver:	n/a	chr7:137376410-137376423 chr7:137376479-137376490 chr7:137376478-137376489 chr7:137376480-137376489 chr7:137376478-137376491
29	CEBPB	chr7:137361741-137361829	HepG2	liver:	n/a	n/a
30	CEBPB	chr7:137376444-137376644	H1-hESC	embryonic stem cell:	n/a	chr7:137376479-137376490 chr7:137376478-137376489 chr7:137376480-137376489 chr7:137376478-137376491
31	CEBPB	chr7:137366917-137367232	K562	blood:	n/a	chr7:137367094-137367105
32	CEBPB	chr7:137388158-137388192	IMR90	lung:	n/a	n/a
33	CEBPB	chr7:137402504-137402779	IMR90	lung:	n/a	n/a
34	CEBPB	chr7:137366975-137367177	HepG2	liver:	n/a	chr7:137367094-137367105
35	CEBPB	chr7:137380788-137381081	HepG2	liver:	n/a	n/a
36	CEBPB	chr7:137384478-137384652	K562	blood:	n/a	chr7:137384574-137384587
37	CHD2	chr7:137387901-137388100	K562	blood:	n/a	n/a
38	CTCF	chr7:137375620-137375770	HAc	cerebellar:	n/a	n/a
39	CTCF	chr7:137371420-137371570	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr7:137403100-137403250	K562	blood:	n/a	n/a
41	CTCF	chr7:137375520-137375670	MCF-7	breast:	n/a	n/a
42	CTCF	chr7:137375500-137375650	GM12874	blood:	n/a	n/a
43	CTCF	chr7:137375440-137375590	BE2_C	brain:	n/a	n/a
44	CTCF	chr7:137361569-137361589	Lung_OC	lung:	n/a	n/a
45	CTCF	chr7:137392054-137392135	Fibrobl	skin:	n/a	n/a
46	CTCF	chr7:137375420-137375570	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr7:137375520-137375670	HRPEpiC	eye:	n/a	n/a
48	CTCF	chr7:137375480-137375630	GM12873	blood:	n/a	n/a
49	CTCF	chr7:137375420-137375570	GM12875	blood:	n/a	n/a
50	CTCF	chr7:137375500-137375650	AG04450	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:137367341-137367391	HMEC	breast:	n/a
2	chr7:137358753-137358803	ProgFib	skin:	n/a
3	chr7:137367341-137367391	AG09309	skin:	n/a
4	chr7:137358753-137358803	NB4	blood:	n/a
5	chr7:137358753-137358803	AoSMC	blood vessel:	n/a
6	chr7:137367341-137367391	GM19239	blood:	n/a
7	chr7:137358753-137358803	GM12891	blood:	n/a
8	chr7:137358753-137358803	K562	blood:	n/a
9	chr7:137358753-137358803	Jurkat	blood:	n/a
10	chr7:137358753-137358803	RPTEC	kidney:	n/a
11	chr7:137358753-137358803	HL-60	blood:	n/a
12	chr7:137358753-137358803	NT2-D1	testis:	n/a
13	chr7:137358753-137358803	SK-N-MC	brain:	n/a
14	chr7:137367341-137367391	HCF	heart:	n/a
15	chr7:137367341-137367391	SK-N-MC	brain:	n/a
16	chr7:137367341-137367391	HUVEC	blood vessel:	n/a
17	chr7:137358753-137358803	BE2_C	brain:	n/a
18	chr7:137358753-137358803	A549	lung:	n/a
19	chr7:137358753-137358803	HRE	kidney:	n/a
20	chr7:137358753-137358803	AG04449	skin:	fetal
21	chr7:137358753-137358803	ovcar-3	ovarian:	n/a
22	chr7:137367341-137367391	SKMC	muscle:	n/a
23	chr7:137358753-137358803	HCPEpiC	choroid plexus:	n/a
24	chr7:137358753-137358803	HCM	heart:	n/a
25	chr7:137367341-137367391	HRCEpiC	kidney:	n/a
26	chr7:137367341-137367391	HRPEpiC	eye:	n/a
27	chr7:137358753-137358803	HAEpiC	amniotic membrane:	n/a
28	chr7:137367341-137367391	RPTEC	kidney:	n/a
29	chr7:137367341-137367391	U87	brain:	n/a
30	chr7:137358753-137358803	BJ	skin:	n/a
31	chr7:137358753-137358803	CMK	blood:	n/a
32	chr7:137367341-137367391	HEEpiC	esophagus:	n/a
33	chr7:137358753-137358803	HepG2	liver:	n/a
34	chr7:137367341-137367391	HAEpiC	amniotic membrane:	n/a
35	chr7:137367341-137367391	Jurkat	blood:	n/a
36	chr7:137358753-137358803	HRCEpiC	kidney:	n/a
37	chr7:137358753-137358803	AG04450	lung:	fetal
38	chr7:137358753-137358803	GM12892	blood:	n/a
39	chr7:137358753-137358803	MCF10A-Er-Src	breast:	n/a
40	chr7:137367341-137367391	MCF-7	breast:	n/a
41	chr7:137358753-137358803	U87	brain:	n/a
42	chr7:137367341-137367391	ovcar-3	ovarian:	n/a
43	chr7:137367341-137367391	HL-60	blood:	n/a
44	chr7:137367341-137367391	NT2-D1	testis:	n/a
45	chr7:137358753-137358803	AG10803	skin:	n/a
46	chr7:137358753-137358803	LNCaP	prostate:	n/a
47	chr7:137358753-137358803	HEEpiC	esophagus:	n/a
48	chr7:137367341-137367391	PFSK-1	brain:	n/a
49	chr7:137367341-137367391	CMK	blood:	n/a
50	chr7:137367341-137367391	MCF10A-Er-Src	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:137369548..137371096-chr7:137379761..137381577,2	K562	blood:
2	chr7:137393034..137395033-chr7:137396178..137398498,3	K562	blood:
3	chr7:137350182..137352785-chr7:137361022..137363744,2	K562	blood:
4	chr7:137400906..137403879-chr7:137418023..137420463,3	K562	blood:
5	chr7:137358034..137360973-chr7:137366222..137368060,2	K562	blood:
6	chr7:137364114..137367092-chr7:137379026..137381477,2	K562	blood:
7	chr7:137369548..137371096-chr7:137379761..137381577,2	K562	blood:
8	chr7:137364114..137367092-chr7:137379026..137381477,2	K562	blood:
9	chr7:137393034..137395033-chr7:137396178..137398498,3	K562	blood:
10	chr7:137358034..137360973-chr7:137366222..137368060,2	K562	blood:
11	chr11:62607010..62609154-chr7:137377166..137379355,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AKR1D1-6	chr7:137356474-137357129	l_3488_chr7:137337580-137357129_testes

Variant related genes	Relation type
ENSG00000230383	TF binding region
ENSG00000230383	CpG island
ENSG00000133316	chromatin interactions

Extended variants
information (count: 1705 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1705 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs270904	chr7:137356651-137356652	Weak transcription Strong transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs142116266	chr7:137356745-137356746	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs192609728	chr7:137356749-137356750	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs184220894	chr7:137356759-137356760	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
5	rs562711434	chr7:137356772-137356773	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs531745495	chr7:137356785-137356786	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs35522978	chr7:137356809-137356810	Weak transcription ZNF genes & repeats Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs3778796	chr7:137356846-137356847	Weak transcription ZNF genes & repeats Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs139499084	chr7:137356868-137356869	Weak transcription ZNF genes & repeats Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs527834490	chr7:137356888-137356889	Weak transcription ZNF genes & repeats Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs541266337	chr7:137356914-137356915	Weak transcription ZNF genes & repeats Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs189595148	chr7:137356916-137356917	Weak transcription ZNF genes & repeats Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs567506166	chr7:137356919-137356920	Weak transcription ZNF genes & repeats Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs181897554	chr7:137356930-137356931	Weak transcription ZNF genes & repeats Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs564671208	chr7:137356936-137356937	Weak transcription ZNF genes & repeats Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs73730089	chr7:137356965-137356966	Weak transcription ZNF genes & repeats Enhancers Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs73454835	chr7:137356985-137356986	Weak transcription ZNF genes & repeats Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs199655606	chr7:137357038-137357039	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs184712991	chr7:137357044-137357045	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs145012954	chr7:137357080-137357081	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
21	rs188911599	chr7:137357099-137357100	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
22	rs147965060	chr7:137357104-137357105	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
23	rs370208517	chr7:137357110-137357111	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
24	rs6969979	chr7:137357111-137357112	Weak transcription Strong transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs563428536	chr7:137357113-137357114	Weak transcription Strong transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
26	rs563208138	chr7:137357177-137357178	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs531561569	chr7:137357236-137357237	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs73730092	chr7:137357255-137357256	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs565174373	chr7:137357425-137357426	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs527774001	chr7:137357444-137357445	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs140067278	chr7:137357498-137357499	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs60078498	chr7:137357539-137357540	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs113823675	chr7:137357540-137357541	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs547941741	chr7:137357568-137357569	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs181333951	chr7:137357573-137357574	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs529931180	chr7:137357589-137357590	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs140626981	chr7:137357596-137357597	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs370988091	chr7:137357600-137357601	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs538594751	chr7:137357612-137357613	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs111276421	chr7:137357629-137357630	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs565364370	chr7:137357641-137357642	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs548962801	chr7:137357659-137357660	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs565641249	chr7:137357660-137357661	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs554259462	chr7:137357662-137357663	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572812382	chr7:137357663-137357664	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs536452365	chr7:137357679-137357680	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs79480898	chr7:137357683-137357684	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs576664719	chr7:137357687-137357688	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs270903	chr7:137357802-137357803	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs145356454	chr7:137357805-137357806	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
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
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	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
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
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21509527	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Neuroticism	17667963	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute myeloid leukemia	17237825	CNVD
Esophageal cancer	21851588	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Bladder cancer	21909424	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell acute lymphoblastic leukemia	16673021	CNVD
Cancer	21183584	CNVD
Intracranial ependymoma	16609018	CNVD
Non-small cell lung cancer	21829676	CNVD
Developmental delay	19490664	CNVD
Pancreatitis	20877625	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD

Chromatin state (count:433 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:137343800-137359000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr7:137344000-137358000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr7:137350400-137356800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr7:137350400-137358000	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr7:137350600-137358000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr7:137351400-137357000	Enhancers	HSMMtube	muscle
7	chr7:137352000-137357000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr7:137352800-137356800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr7:137353600-137357400	Enhancers	Muscle Satellite Cultured Cells	--
10	chr7:137354600-137357000	Enhancers	Fetal Brain Male	brain
11	chr7:137355000-137357000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr7:137355800-137356800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr7:137355800-137356800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr7:137355800-137356800	Weak transcription	Left Ventricle	heart
15	chr7:137355800-137357400	Enhancers	Osteobl	bone
16	chr7:137355800-137370600	Weak transcription	Aorta	Aorta
17	chr7:137356000-137361800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr7:137356200-137357800	Weak transcription	NHDF-Ad	bronchial
19	chr7:137356400-137356800	Weak transcription	Brain Anterior Caudate	brain
20	chr7:137356400-137365800	Weak transcription	HSMM	muscle
21	chr7:137356600-137357000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
22	chr7:137356600-137357000	Enhancers	Fetal Heart	heart
23	chr7:137356600-137358600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr7:137356800-137357000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr7:137356800-137357000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr7:137356800-137357000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr7:137356800-137357000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr7:137356800-137357000	Enhancers	Left Ventricle	heart
29	chr7:137356800-137357400	Enhancers	Brain Anterior Caudate	brain
30	chr7:137357000-137358400	Weak transcription	HSMMtube	muscle
31	chr7:137357000-137359400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr7:137357000-137366400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr7:137357000-137367600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr7:137357200-137361000	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr7:137357400-137360800	Weak transcription	Muscle Satellite Cultured Cells	--
36	chr7:137357400-137365600	Weak transcription	Osteobl	bone
37	chr7:137357800-137358000	Enhancers	NHDF-Ad	bronchial
38	chr7:137358000-137359400	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr7:137358000-137359600	Enhancers	H1 Cell Line	embryonic stem cell
40	chr7:137358000-137359600	Enhancers	H9 Cell Line	embryonic stem cell
41	chr7:137358000-137360000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr7:137358000-137360200	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr7:137358000-137360600	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr7:137358000-137360800	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr7:137358200-137359800	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr7:137358200-137361000	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr7:137358400-137358600	Enhancers	HSMMtube	muscle
48	chr7:137358600-137359000	Weak transcription	HSMMtube	muscle
49	chr7:137358600-137360600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr7:137359000-137359200	Enhancers	ES-WA7 Cell Line	embryonic stem cell

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