Variant report

Variant	nsv1032610
Chromosome Location	chr7:84683282-84725413
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	CEBPB	chr7:84722987-84723198	HepG2	liver:	n/a	chr7:84723072-84723083
2	CEBPB	chr7:84698114-84698707	IMR90	lung:	n/a	n/a
3	CEBPB	chr7:84716026-84716363	IMR90	lung:	n/a	chr7:84716195-84716206 chr7:84716195-84716208
4	CEBPB	chr7:84716021-84716380	A549	lung:	n/a	chr7:84716195-84716206 chr7:84716195-84716208
5	CEBPB	chr7:84698240-84698528	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr7:84722951-84723231	IMR90	lung:	n/a	chr7:84723072-84723083
7	CEBPB	chr7:84700492-84701473	IMR90	lung:	n/a	n/a
8	CEBPB	chr7:84716033-84716591	HepG2	liver:	n/a	chr7:84716195-84716206 chr7:84716195-84716208
9	CEBPB	chr7:84700274-84700807	ECC-1	luminal epithelium:	n/a	n/a
10	CEBPB	chr7:84716035-84716343	H1-hESC	embryonic stem cell:	n/a	chr7:84716195-84716206 chr7:84716195-84716208
11	CTCF	chr7:84700600-84700750	AG04449	skin:	n/a	n/a
12	CTCF	chr7:84700520-84700670	HBMEC	blood vessel:	n/a	n/a
13	CTCF	chr7:84695560-84695710	GM12875	blood:	n/a	n/a
14	E2F4	chr7:84706573-84706762	MCF10A-Er-Src	breast:	n/a	n/a
15	EP300	chr7:84719099-84719971	SK-N-SH	brain:	n/a	n/a
16	EP300	chr7:84700084-84700933	ECC-1	luminal epithelium:	n/a	n/a
17	EP300	chr7:84719414-84719943	SK-N-SH_RA	brain:	n/a	n/a
18	EP300	chr7:84700218-84700962	SK-N-SH	brain:	n/a	n/a
19	EP300	chr7:84719377-84720030	SK-N-SH_RA	brain:	n/a	n/a
20	ESR1	chr7:84703318-84703683	ECC-1	luminal epithelium:	n/a	n/a
21	ESR1	chr7:84699875-84700865	ECC-1	luminal epithelium:	n/a	n/a
22	FOS	chr7:84716086-84716204	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr7:84698220-84698575	MCF10A-Er-Src	breast:	n/a	chr7:84698403-84698415 chr7:84698404-84698414 chr7:84698405-84698412 chr7:84698403-84698414 chr7:84698405-84698414 chr7:84698404-84698414 chr7:84698406-84698417 chr7:84698404-84698413
24	FOS	chr7:84700783-84700966	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr7:84698214-84698583	MCF10A-Er-Src	breast:	n/a	chr7:84698403-84698415 chr7:84698404-84698414 chr7:84698405-84698412 chr7:84698403-84698414 chr7:84698405-84698414 chr7:84698404-84698414 chr7:84698406-84698417 chr7:84698404-84698413
26	FOS	chr7:84698227-84698574	MCF10A-Er-Src	breast:	n/a	chr7:84698403-84698415 chr7:84698404-84698414 chr7:84698405-84698412 chr7:84698403-84698414 chr7:84698405-84698414 chr7:84698404-84698414 chr7:84698406-84698417 chr7:84698404-84698413
27	FOS	chr7:84700710-84700951	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr7:84698220-84698588	MCF10A-Er-Src	breast:	n/a	chr7:84698403-84698415 chr7:84698404-84698414 chr7:84698405-84698412 chr7:84698403-84698414 chr7:84698405-84698414 chr7:84698404-84698414 chr7:84698406-84698417 chr7:84698404-84698413
29	FOS	chr7:84698175-84698600	HUVEC	blood vessel:	n/a	chr7:84698403-84698415 chr7:84698404-84698414 chr7:84698405-84698412 chr7:84698403-84698414 chr7:84698405-84698414 chr7:84698404-84698414 chr7:84698406-84698417 chr7:84698404-84698413
30	FOSL2	chr7:84700328-84701074	SK-N-SH	brain:	n/a	n/a
31	FOSL2	chr7:84698150-84698693	SK-N-SH	brain:	n/a	chr7:84698403-84698415 chr7:84698404-84698414 chr7:84698405-84698412 chr7:84698405-84698414 chr7:84698404-84698414 chr7:84698406-84698417 chr7:84698404-84698413
32	FOSL2	chr7:84698060-84698640	SK-N-SH	brain:	n/a	chr7:84698403-84698415 chr7:84698404-84698414 chr7:84698405-84698412 chr7:84698405-84698414 chr7:84698404-84698414 chr7:84698406-84698417 chr7:84698404-84698413
33	FOSL2	chr7:84698259-84698473	HepG2	liver:	n/a	chr7:84698403-84698415 chr7:84698404-84698414 chr7:84698405-84698412 chr7:84698405-84698414 chr7:84698404-84698414 chr7:84698406-84698417 chr7:84698404-84698413
34	FOXA1	chr7:84703326-84703506	ECC-1	luminal epithelium:	n/a	chr7:84703432-84703444
35	FOXA1	chr7:84695201-84695379	ECC-1	luminal epithelium:	n/a	chr7:84695274-84695286
36	FOXA1	chr7:84703203-84703648	ECC-1	luminal epithelium:	n/a	chr7:84703432-84703444
37	FOXP2	chr7:84707620-84707864	SK-N-MC	brain:	n/a	n/a
38	FOXP2	chr7:84710777-84711005	SK-N-MC	brain:	n/a	n/a
39	GATA3	chr7:84704772-84705384	SK-N-SH	brain:	n/a	chr7:84705101-84705108 chr7:84704774-84704784 chr7:84705099-84705108
40	GATA3	chr7:84700158-84701109	SK-N-SH	brain:	n/a	chr7:84700489-84700496
41	GATA3	chr7:84700199-84701172	SK-N-SH	brain:	n/a	chr7:84700489-84700496
42	GATA3	chr7:84704742-84705456	SK-N-SH	brain:	n/a	chr7:84705101-84705108 chr7:84704774-84704784 chr7:84705099-84705108
43	GATA3	chr7:84685227-84685649	SH-SY5Y	brain:	n/a	n/a
44	GATA3	chr7:84685270-84685543	MCF-7	breast:	n/a	n/a
45	GATA3	chr7:84685120-84685729	MCF-7	breast:	n/a	n/a
46	GATA3	chr7:84697987-84698709	SK-N-SH	brain:	n/a	chr7:84698406-84698415
47	GATA3	chr7:84685289-84685487	T-47D	breast:	n/a	n/a
48	GATA3	chr7:84697982-84698739	SK-N-SH	brain:	n/a	chr7:84698406-84698415
49	GATA3	chr7:84689236-84689255	SH-SY5Y	brain:	n/a	n/a
50	JUN	chr7:84704292-84704402	HepG2	liver:	n/a	chr7:84704382-84704389 chr7:84704334-84704347

No.	Distal block	Cell Line	Cell type
1	chr7:84689168..84690751-chr7:84693182..84694886,2	K562	blood:
2	chr7:84710975..84713239-chr7:84714640..84716583,2	K562	blood:
3	chr7:84694165..84696935-chr7:84697891..84700074,2	K562	blood:
4	chr7:84692893..84695665-chr7:84697192..84699391,2	K562	blood:
5	chr7:84692893..84695665-chr7:84697192..84699391,2	K562	blood:
6	chr7:84717702..84719769-chr7:84720076..84722909,2	K562	blood:
7	chr7:84694165..84696935-chr7:84697891..84700074,2	K562	blood:
8	chr7:84710975..84713239-chr7:84714640..84716583,2	K562	blood:
9	chr7:84689168..84690751-chr7:84693182..84694886,2	K562	blood:
10	chr7:84717702..84719769-chr7:84720076..84722909,2	K562	blood:
11	chr7:84718632..84720833-chr7:84723046..84725256,2	K562	blood:
12	chr7:84718632..84720833-chr7:84723046..84725256,2	K562	blood:

Variant related genes	Relation type
SEMA3D	TF binding region

Extended variants
information (count: 1483 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1483 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374864304	chr7:84683283-84683284	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs577147529	chr7:84683300-84683301	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs77760597	chr7:84683350-84683351	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs144509266	chr7:84683351-84683352	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs577564764	chr7:84683386-84683387	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs530228944	chr7:84683399-84683400	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs551100269	chr7:84683422-84683423	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs150613922	chr7:84683470-84683471	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs78157024	chr7:84683551-84683552	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560309525	chr7:84683789-84683790	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs527963777	chr7:84683792-84683793	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs552630948	chr7:84683820-84683821	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs77173412	chr7:84683880-84683881	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs7811875	chr7:84683935-84683936	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs371691944	chr7:84683990-84683991	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs377084465	chr7:84684107-84684108	Weak transcription Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs149793566	chr7:84684206-84684207	Weak transcription Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs187284049	chr7:84684214-84684215	Weak transcription Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs554525813	chr7:84684256-84684257	Weak transcription Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs192611790	chr7:84684288-84684289	Weak transcription Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs534083223	chr7:84684292-84684293	Weak transcription Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs558623656	chr7:84684338-84684339	Weak transcription Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs59006756	chr7:84684392-84684393	Weak transcription Enhancers Active TSS Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs538000105	chr7:84684462-84684463	Weak transcription Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs112623813	chr7:84684463-84684464	Weak transcription Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs547239651	chr7:84684513-84684514	Weak transcription Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs184538640	chr7:84684523-84684524	Weak transcription Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs145776047	chr7:84684582-84684583	Weak transcription Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs76289807	chr7:84684583-84684584	Weak transcription Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs374034657	chr7:84684629-84684630	Weak transcription Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs572390620	chr7:84684684-84684685	Weak transcription Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs377702909	chr7:84684686-84684687	Weak transcription Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs187457106	chr7:84684690-84684691	Weak transcription Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs564398244	chr7:84684691-84684692	Weak transcription Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs546823355	chr7:84684756-84684757	Weak transcription Enhancers Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs555489742	chr7:84684807-84684808	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs140002212	chr7:84684857-84684858	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs549933711	chr7:84684900-84684901	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs544796529	chr7:84684925-84684926	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs199946932	chr7:84684962-84684963	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs60798714	chr7:84684996-84684997	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs56131427	chr7:84684998-84684999	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs57323073	chr7:84685017-84685018	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs193256257	chr7:84685021-84685022	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs371170073	chr7:84685022-84685023	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs201852843	chr7:84685026-84685027	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs566459043	chr7:84685041-84685042	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs200541130	chr7:84685048-84685049	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs552162067	chr7:84685072-84685073	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs150804633	chr7:84685079-84685080	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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

Chromatin state (count:216 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:84656200-84694800	Weak transcription	Fetal Stomach	stomach
2	chr7:84676400-84683600	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr7:84676400-84694800	Weak transcription	Colon Smooth Muscle	Colon
4	chr7:84678400-84689800	Weak transcription	Aorta	Aorta
5	chr7:84679000-84683800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr7:84679200-84692600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr7:84679400-84683600	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr7:84680400-84694600	Weak transcription	Fetal Kidney	kidney
9	chr7:84681000-84684600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr7:84681600-84684800	Strong transcription	Fetal Lung	lung
11	chr7:84682400-84684400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr7:84682400-84684800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr7:84682400-84685600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr7:84683000-84683400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr7:84683400-84684800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr7:84683600-84684000	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr7:84683600-84684000	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr7:84683600-84684000	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr7:84683600-84684000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr7:84683600-84684200	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr7:84683600-84684200	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr7:84683600-84684400	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr7:84683600-84685600	Enhancers	NHEK	skin
24	chr7:84683800-84684000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr7:84683800-84684000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr7:84683800-84684000	Enhancers	Fetal Muscle Leg	muscle
27	chr7:84683800-84685800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr7:84684000-84685600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr7:84684000-84700000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr7:84684400-84695000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr7:84684600-84684800	Enhancers	HMEC	breast
32	chr7:84684600-84685800	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr7:84684800-84689800	Weak transcription	Fetal Lung	lung
34	chr7:84685400-84685600	Enhancers	HMEC	breast
35	chr7:84685600-84685800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr7:84685600-84685800	Flanking Active TSS	NHEK	skin
37	chr7:84685800-84686800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr7:84685800-84695600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr7:84686800-84687400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
40	chr7:84687400-84695200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr7:84689400-84690000	Enhancers	Fetal Heart	heart
42	chr7:84689800-84690000	Enhancers	Aorta	Aorta
43	chr7:84689800-84690000	Enhancers	Spleen	Spleen
44	chr7:84689800-84692200	Enhancers	Fetal Lung	lung
45	chr7:84690000-84691000	Weak transcription	Spleen	Spleen
46	chr7:84691000-84691400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr7:84691000-84691400	Enhancers	Spleen	Spleen
48	chr7:84691200-84691400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr7:84691400-84693000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr7:84692200-84692400	Genic enhancers	Fetal Lung	lung

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