Variant report

Variant	nsv971172
Chromosome Location	chr7:65616238-65653268
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:481)
CpG islands
(count:246)
Chromatin interactive
region (count:15)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:481 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:65622130-65622328	K562	blood:	n/a	n/a
2	ARID3A	chr7:65632999-65633320	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:65648902-65649056	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:65646362-65646381	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:65635993-65636265	HepG2	liver:	n/a	n/a
6	ATF3	chr7:65643272-65643517	K562	blood:	n/a	n/a
7	BACH1	chr7:65622174-65622444	K562	blood:	n/a	n/a
8	BATF	chr7:65627677-65627935	GM12878	blood:	n/a	n/a
9	BHLHE40	chr7:65622160-65622476	K562	blood:	n/a	n/a
10	BHLHE40	chr7:65635242-65635605	K562	blood:	n/a	chr7:65635359-65635368 chr7:65635359-65635368
11	BHLHE40	chr7:65643276-65643552	K562	blood:	n/a	n/a
12	CBX3	chr7:65650785-65651176	K562	blood:	n/a	n/a
13	CBX3	chr7:65643216-65643628	K562	blood:	n/a	n/a
14	CBX3	chr7:65643147-65643681	K562	blood:	n/a	n/a
15	CCNT2	chr7:65622193-65622473	K562	blood:	n/a	n/a
16	CEBPB	chr7:65635259-65635577	K562	blood:	n/a	chr7:65635423-65635434
17	CEBPB	chr7:65647859-65648326	HepG2	liver:	n/a	n/a
18	CEBPB	chr7:65629007-65629306	A549	lung:	n/a	n/a
19	CEBPB	chr7:65621166-65621311	HepG2	liver:	n/a	n/a
20	CEBPB	chr7:65635242-65635615	HepG2	liver:	n/a	chr7:65635423-65635434
21	CEBPB	chr7:65648040-65648318	IMR90	lung:	n/a	n/a
22	CEBPB	chr7:65632992-65633357	IMR90	lung:	n/a	n/a
23	CEBPB	chr7:65617114-65617506	IMR90	lung:	n/a	n/a
24	CEBPB	chr7:65633008-65633300	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr7:65621035-65621396	A549	lung:	n/a	n/a
26	CEBPB	chr7:65621070-65621271	K562	blood:	n/a	n/a
27	CEBPB	chr7:65621052-65621400	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr7:65628157-65628414	HepG2	liver:	n/a	chr7:65628236-65628247
29	CEBPB	chr7:65648746-65649050	IMR90	lung:	n/a	n/a
30	CEBPB	chr7:65635319-65635524	HepG2	liver:	n/a	chr7:65635423-65635434
31	CEBPB	chr7:65628999-65629305	IMR90	lung:	n/a	n/a
32	CEBPB	chr7:65635264-65635560	ECC-1	luminal epithelium:	n/a	chr7:65635423-65635434
33	CEBPB	chr7:65621033-65621416	K562	blood:	n/a	n/a
34	CEBPB	chr7:65647922-65648283	HepG2	liver:	n/a	n/a
35	CEBPB	chr7:65621037-65621407	HepG2	liver:	n/a	n/a
36	CEBPB	chr7:65628978-65629290	HepG2	liver:	n/a	n/a
37	CEBPB	chr7:65635239-65635622	K562	blood:	n/a	chr7:65635423-65635434
38	CEBPB	chr7:65635338-65635618	ECC-1	luminal epithelium:	n/a	chr7:65635423-65635434
39	CEBPB	chr7:65635922-65636282	A549	lung:	n/a	n/a
40	CEBPB	chr7:65647972-65648231	HepG2	liver:	n/a	n/a
41	CEBPB	chr7:65636084-65636215	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr7:65621012-65621396	ECC-1	luminal epithelium:	n/a	n/a
43	CEBPB	chr7:65652907-65653260	HepG2	liver:	n/a	chr7:65653073-65653086 chr7:65653073-65653084
44	CEBPB	chr7:65621136-65621349	MCF-7	breast:	n/a	n/a
45	CEBPB	chr7:65635267-65635565	MCF-7	breast:	n/a	chr7:65635423-65635434
46	CEBPB	chr7:65635264-65636298	Hela-S3	cervix:	n/a	chr7:65635423-65635434
47	CEBPB	chr7:65621041-65621402	IMR90	lung:	n/a	n/a
48	CEBPB	chr7:65653058-65653143	Hela-S3	cervix:	n/a	chr7:65653073-65653086 chr7:65653073-65653084
49	CEBPB	chr7:65649445-65649706	HepG2	liver:	n/a	n/a
50	CEBPB	chr7:65621075-65621321	H1-hESC	embryonic stem cell:	n/a	n/a

(count:246 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:65617362-65617412	HCF	heart:	n/a
2	chr7:65647940-65647990	NHBE	bronchial:	n/a
3	chr7:65617362-65617412	HCF	heart:	n/a
4	chr7:65647940-65647990	NHBE	bronchial:	n/a
5	chr7:65647940-65647990	T-47D	breast:	n/a
6	chr7:65647940-65647990	HNPCEpiC	eye:	n/a
7	chr7:65635328-65635378	GM12891	blood:	n/a
8	chr7:65647940-65647990	AG10803	skin:	n/a
9	chr7:65617362-65617412	PFSK-1	brain:	n/a
10	chr7:65617362-65617412	SKMC	muscle:	n/a
11	chr7:65647879-65647929	Hela-S3	cervix:	n/a
12	chr7:65617362-65617412	MCF-7	breast:	n/a
13	chr7:65635328-65635378	NHBE	bronchial:	n/a
14	chr7:65635328-65635378	NH-A	brain:	n/a
15	chr7:65647940-65647990	HIPEpiC	eye:	n/a
16	chr7:65647879-65647929	SAEC	small airway:	n/a
17	chr7:65617362-65617412	HPAEpiC	pulmonary alveolar:	n/a
18	chr7:65635328-65635378	HCM	heart:	n/a
19	chr7:65617362-65617412	BJ	skin:	n/a
20	chr7:65635328-65635378	HL-60	blood:	n/a
21	chr7:65635328-65635378	HNPCEpiC	eye:	n/a
22	chr7:65635328-65635378	MCF-7	breast:	n/a
23	chr7:65647940-65647990	SAEC	small airway:	n/a
24	chr7:65647940-65647990	SK-N-SH	brain:	n/a
25	chr7:65617362-65617412	HL-60	blood:	n/a
26	chr7:65647879-65647929	NT2-D1	testis:	n/a
27	chr7:65635328-65635378	ECC-1	luminal epithelium:	n/a
28	chr7:65635328-65635378	HEK293	kidney:	embryo
29	chr7:65635328-65635378	GM12878	blood:	n/a
30	chr7:65647879-65647929	Jurkat	blood:	n/a
31	chr7:65617362-65617412	HAEpiC	amniotic membrane:	n/a
32	chr7:65647940-65647990	HCM	heart:	n/a
33	chr7:65647940-65647990	Jurkat	blood:	n/a
34	chr7:65635328-65635378	IMR90	lung:	fetal
35	chr7:65617362-65617412	Hela-S3	cervix:	n/a
36	chr7:65647879-65647929	SK-N-SH	brain:	n/a
37	chr7:65647940-65647990	GM12878	blood:	n/a
38	chr7:65647879-65647929	HRE	kidney:	n/a
39	chr7:65617362-65617412	Caco-2	colon:	n/a
40	chr7:65635328-65635378	PrEC	prostate:	n/a
41	chr7:65647879-65647929	HCM	heart:	n/a
42	chr7:65647879-65647929	HRPEpiC	eye:	n/a
43	chr7:65647879-65647929	GM12891	blood:	n/a
44	chr7:65647940-65647990	NT2-D1	testis:	n/a
45	chr7:65617362-65617412	NT2-D1	testis:	n/a
46	chr7:65635328-65635378	Hela-S3	cervix:	n/a
47	chr7:65647940-65647990	HCPEpiC	choroid plexus:	n/a
48	chr7:65635328-65635378	HMEC	breast:	n/a
49	chr7:65647879-65647929	A549	lung:	n/a
50	chr7:65647879-65647929	GM12878	blood:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:65617048..65619822-chr7:65625013..65626809,2	MCF-7	breast:
2	chr7:65630028..65632424-chr7:65633980..65636859,2	K562	blood:
3	chr7:65630028..65632424-chr7:65633980..65636859,2	K562	blood:
4	chr7:65633079..65635754-chr7:65815405..65818400,2	K562	blood:
5	chr7:65649367..65652359-chr7:65653960..65655617,2	K562	blood:
6	chr7:65611050..65612887-chr7:65620053..65622926,2	K562	blood:
7	chr7:65446691..65448444-chr7:65618479..65620177,2	K562	blood:
8	chr7:65625074..65627224-chr7:65631943..65634316,2	K562	blood:
9	chr7:65540658..65542432-chr7:65622209..65624155,2	K562	blood:
10	chr7:65625074..65627224-chr7:65631943..65634316,2	K562	blood:
11	chr7:65640707..65643373-chr7:65647388..65648894,2	K562	blood:
12	chr7:65640707..65643373-chr7:65647388..65648894,2	K562	blood:
13	chr7:65617048..65619822-chr7:65625013..65626809,2	MCF-7	breast:
14	chr7:65613342..65615029-chr7:65615766..65618205,2	MCF-7	breast:
15	chr7:65614360..65616994-chr7:65636358..65639293,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GUSB-4	chr7:65617658-65618970	ENSG00000245589
2	lnc-GUSB-3	chr7:65629970-65629998	ENSG00000234185.2
3	lnc-GUSB-4	chr7:65619245-65619549	ENSG00000245589

No data

Variant related genes	Relation type
ENSG00000234185	TF binding region
ENSG00000234185	CpG island
ENSG00000169919	chromatin interactions
ENSG00000126522	chromatin interactions
ENSG00000241258	chromatin interactions
ENSG00000169902	chromatin interactions
SIRT1	miRNA target sites

Extended variants
information (count: 1385 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1385 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534087874	chr7:65616239-65616240	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
2	rs373214743	chr7:65616290-65616291	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
3	rs181265000	chr7:65616295-65616296	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
4	rs528131769	chr7:65616299-65616300	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
5	rs572100977	chr7:65616357-65616358	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
6	rs532257744	chr7:65616398-65616399	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
7	rs551980278	chr7:65616401-65616402	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs116984296	chr7:65616419-65616420	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs537564681	chr7:65616435-65616436	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs183853270	chr7:65616533-65616534	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs567967751	chr7:65616557-65616558	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs143133173	chr7:65616561-65616562	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs78439535	chr7:65616562-65616563	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs148236050	chr7:65616563-65616564	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs7779258	chr7:65616587-65616588	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs546500991	chr7:65616596-65616597	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs316303	chr7:65616623-65616624	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs189309234	chr7:65616626-65616627	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs13223921	chr7:65616648-65616649	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs141979300	chr7:65616654-65616655	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs34143961	chr7:65616660-65616661	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs62465481	chr7:65616662-65616663	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs113338652	chr7:65616663-65616664	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs62465482	chr7:65616664-65616665	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs113170482	chr7:65616665-65616666	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs112589222	chr7:65616666-65616667	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs144946397	chr7:65616734-65616735	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs376797256	chr7:65616738-65616739	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs10256691	chr7:65616739-65616740	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
30	rs562254722	chr7:65616761-65616762	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs369701906	chr7:65616782-65616783	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs527774349	chr7:65616810-65616811	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs374428276	chr7:65616840-65616841	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs77257935	chr7:65616843-65616844	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs180807227	chr7:65616871-65616872	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs78469253	chr7:65616883-65616884	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs316304	chr7:65616894-65616895	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs200724302	chr7:65616905-65616906	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs150369233	chr7:65616935-65616936	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs538651956	chr7:65616957-65616958	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs568721003	chr7:65617050-65617051	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
42	rs138076238	chr7:65617051-65617052	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
43	rs548081975	chr7:65617059-65617060	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
44	rs568190207	chr7:65617060-65617061	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
45	rs113324236	chr7:65617071-65617072	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
46	rs553833961	chr7:65617107-65617108	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
47	rs570424872	chr7:65617133-65617134	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
48	rs373264589	chr7:65617150-65617151	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
49	rs376463571	chr7:65617197-65617198	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
50	rs371302904	chr7:65617216-65617217	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
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
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
Follicular lymphoma	20505157	CNVD
Biliary cancer	19435499	CNVD
Williams-beuren syndrome	22470819	CNVD
Acute lymphoblastic leukemia	20067559	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
T-cell prolymphocytic leukemia	17713554	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	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
Glioblastoma	21080181	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
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD

Chromatin state (count:748 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:65581000-65617200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr7:65595200-65622000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
3	chr7:65595600-65623200	Strong transcription	Dnd41	blood
4	chr7:65595600-65623800	Strong transcription	Primary T cells from cord blood	blood
5	chr7:65595800-65617200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
6	chr7:65595800-65620000	Strong transcription	Primary neutrophils fromperipheralblood	blood
7	chr7:65599200-65623400	Strong transcription	Primary B cells from peripheral blood	blood
8	chr7:65606600-65617600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr7:65607400-65617000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr7:65608200-65617000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr7:65609000-65622400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr7:65609200-65623200	Weak transcription	Fetal Brain Male	brain
13	chr7:65609200-65623400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr7:65609600-65624600	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr7:65610400-65617000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr7:65611200-65617000	Enhancers	NHDF-Ad	bronchial
17	chr7:65612000-65635400	Weak transcription	Fetal Kidney	kidney
18	chr7:65612600-65617000	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr7:65612600-65617000	Weak transcription	Aorta	Aorta
20	chr7:65612800-65617000	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr7:65613600-65621600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr7:65613800-65617000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr7:65614000-65617200	Enhancers	HUVEC	blood vessel
24	chr7:65614200-65616800	Enhancers	HepG2	liver
25	chr7:65614200-65620000	Strong transcription	GM12878-XiMat	blood
26	chr7:65614800-65618200	Enhancers	Right Atrium	heart
27	chr7:65615200-65616600	Flanking Active TSS	Liver	Liver
28	chr7:65615200-65616600	Enhancers	Osteobl	bone
29	chr7:65615200-65617000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr7:65615200-65617200	Strong transcription	HUES48 Cell Line	embryonic stem cell
31	chr7:65615200-65618000	Genic enhancers	Fetal Muscle Leg	muscle
32	chr7:65615200-65618200	Genic enhancers	Fetal Muscle Trunk	muscle
33	chr7:65615200-65618400	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr7:65615200-65618400	Genic enhancers	Fetal Stomach	stomach
35	chr7:65615200-65622600	Strong transcription	Fetal Brain Female	brain
36	chr7:65615200-65623400	Strong transcription	Primary monocytes fromperipheralblood	blood
37	chr7:65615200-65623800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr7:65615200-65623800	Strong transcription	Monocytes-CD14+_RO01746	blood
39	chr7:65615400-65616400	Enhancers	Colon Smooth Muscle	Colon
40	chr7:65615400-65616400	Genic enhancers	Duodenum Smooth Muscle	Duodenum
41	chr7:65615400-65616400	Genic enhancers	Esophagus	oesophagus
42	chr7:65615400-65616600	Enhancers	Left Ventricle	heart
43	chr7:65615400-65616800	Enhancers	Brain Substantia Nigra	brain
44	chr7:65615400-65617000	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr7:65615400-65617000	Enhancers	Right Ventricle	heart
46	chr7:65615400-65617000	Enhancers	NH-A	brain
47	chr7:65615400-65617800	Genic enhancers	Brain Cingulate Gyrus	brain
48	chr7:65615400-65617800	Genic enhancers	Brain Inferior Temporal Lobe	brain
49	chr7:65615400-65618000	Genic enhancers	Pancreas	Pancrea
50	chr7:65615400-65618000	Genic enhancers	Rectal Mucosa Donor 31	rectum

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