Variant report

Variant	esv1795864
Chromosome Location	chr7:98013507-98040788
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:857)
CpG islands
(count:793)
Chromatin interactive
region (count:28)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:857 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:98028371-98029207	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:98030332-98030731	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:98028495-98029325	K562	blood:	n/a	n/a
4	ATF2	chr7:98030506-98030877	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr7:98028299-98028891	K562	blood:	n/a	n/a
6	BACH1	chr7:98028395-98028741	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr7:98030655-98030848	K562	blood:	n/a	n/a
8	BACH1	chr7:98034182-98034476	H1-hESC	embryonic stem cell:	n/a	chr7:98034309-98034323
9	BACH1	chr7:98030491-98030880	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr7:98028679-98028954	GM12878	blood:	n/a	chr7:98028794-98028805
11	BATF	chr7:98015317-98015518	GM12878	blood:	n/a	n/a
12	BATF	chr7:98015682-98015874	GM12878	blood:	n/a	n/a
13	BCL3	chr7:98029874-98030259	GM12878	blood:	n/a	n/a
14	BCL3	chr7:98039093-98039502	A549	lung:	n/a	n/a
15	BCL3	chr7:98029764-98030361	A549	lung:	n/a	n/a
16	BCL3	chr7:98029781-98030232	A549	lung:	n/a	n/a
17	BCLAF1	chr7:98028622-98029025	GM12878	blood:	n/a	chr7:98028822-98028831
18	BCLAF1	chr7:98030078-98030860	GM12878	blood:	n/a	n/a
19	BHLHE40	chr7:98031286-98031486	K562	blood:	n/a	n/a
20	BHLHE40	chr7:98030505-98030866	GM12878	blood:	n/a	n/a
21	BHLHE40	chr7:98030486-98030812	K562	blood:	n/a	n/a
22	BHLHE40	chr7:98028084-98028406	K562	blood:	n/a	n/a
23	BHLHE40	chr7:98030495-98030828	HepG2	liver:	n/a	n/a
24	BHLHE40	chr7:98029995-98030226	GM12878	blood:	n/a	n/a
25	BHLHE40	chr7:98030050-98030211	K562	blood:	n/a	n/a
26	BHLHE40	chr7:98031272-98031460	HepG2	liver:	n/a	n/a
27	BHLHE40	chr7:98029319-98029455	K562	blood:	n/a	n/a
28	BRCA1	chr7:98030622-98030725	HepG2	liver:	n/a	n/a
29	BRCA1	chr7:98030534-98030739	Hela-S3	cervix:	n/a	n/a
30	CBX3	chr7:98029872-98030832	K562	blood:	n/a	n/a
31	CCNT2	chr7:98029980-98030816	K562	blood:	n/a	n/a
32	CEBPB	chr7:98023720-98024173	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr7:98014693-98014841	K562	blood:	n/a	chr7:98014788-98014799
34	CEBPB	chr7:98027923-98028315	K562	blood:	n/a	chr7:98027954-98027971 chr7:98027956-98027967
35	CEBPB	chr7:98027767-98028559	A549	lung:	n/a	chr7:98027954-98027971 chr7:98027956-98027967
36	CEBPB	chr7:98027886-98028086	HepG2	liver:	n/a	chr7:98027954-98027971 chr7:98027956-98027967
37	CEBPB	chr7:98014722-98014852	A549	lung:	n/a	chr7:98014788-98014799
38	CEBPB	chr7:98039257-98039455	A549	lung:	n/a	n/a
39	CEBPB	chr7:98023581-98024151	A549	lung:	n/a	n/a
40	CEBPB	chr7:98023732-98023988	IMR90	lung:	n/a	n/a
41	CEBPB	chr7:98030181-98030776	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr7:98014736-98014874	HepG2	liver:	n/a	chr7:98014788-98014799
43	CEBPB	chr7:98021670-98021907	HepG2	liver:	n/a	chr7:98021755-98021766
44	CEBPD	chr7:98030106-98030834	HepG2	liver:	n/a	n/a
45	CHD1	chr7:98028783-98029273	GM12878	blood:	n/a	n/a
46	CHD1	chr7:98030052-98030396	GM12878	blood:	n/a	n/a
47	CHD1	chr7:98030067-98030278	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr7:98029512-98030870	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr7:98023786-98024105	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr7:98028885-98029640	GM12878	blood:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:98028207-98028257	GM19239	blood:	n/a
2	chr7:98026481-98026531	GM19239	blood:	n/a
3	chr7:98030641-98030691	AG04450	lung:	fetal
4	chr7:98030098-98030148	U87	brain:	n/a
5	chr7:98031846-98031896	NH-A	brain:	n/a
6	chr7:98029266-98029316	HCT-116	colon:	n/a
7	chr7:98030098-98030148	NHBE	bronchial:	n/a
8	chr7:98030098-98030148	HRE	kidney:	n/a
9	chr7:98029266-98029316	H1-hESC	embryonic stem cell:	embryo
10	chr7:98030482-98030532	BE2_C	brain:	n/a
11	chr7:98032586-98032636	GM12892	blood:	n/a
12	chr7:98031846-98031896	MCF10A-Er-Src	breast:	n/a
13	chr7:98030477-98030527	NB4	blood:	n/a
14	chr7:98029285-98029335	HAEpiC	amniotic membrane:	n/a
15	chr7:98032586-98032636	H1-hESC	embryonic stem cell:	embryo
16	chr7:98028207-98028257	GM06990	blood:	n/a
17	chr7:98030324-98030374	HMEC	breast:	n/a
18	chr7:98030280-98030330	ECC-1	luminal epithelium:	n/a
19	chr7:98030477-98030527	HPAEpiC	pulmonary alveolar:	n/a
20	chr7:98030641-98030691	ovcar-3	ovarian:	n/a
21	chr7:98030477-98030527	PFSK-1	brain:	n/a
22	chr7:98030280-98030330	HPAEpiC	pulmonary alveolar:	n/a
23	chr7:98030482-98030532	AG04449	skin:	fetal
24	chr7:98026481-98026531	HNPCEpiC	eye:	n/a
25	chr7:98029285-98029335	NHBE	bronchial:	n/a
26	chr7:98030324-98030374	U87	brain:	n/a
27	chr7:98032586-98032636	SK-N-SH	brain:	n/a
28	chr7:98032586-98032636	HEK293	kidney:	embryo
29	chr7:98030477-98030527	HNPCEpiC	eye:	n/a
30	chr7:98030477-98030527	ProgFib	skin:	n/a
31	chr7:98030795-98030845	HEK293	kidney:	embryo
32	chr7:98030098-98030148	HL-60	blood:	n/a
33	chr7:98030280-98030330	CMK	blood:	n/a
34	chr7:98031846-98031896	GM06990	blood:	n/a
35	chr7:98026481-98026531	PANC-1	pancreas:	n/a
36	chr7:98030324-98030374	PrEC	prostate:	n/a
37	chr7:98030280-98030330	RPTEC	kidney:	n/a
38	chr7:98029266-98029316	HRPEpiC	eye:	n/a
39	chr7:98029285-98029335	HL-60	blood:	n/a
40	chr7:98030324-98030374	HRCEpiC	kidney:	n/a
41	chr7:98030280-98030330	SK-N-SH_RA	brain:	n/a
42	chr7:98030477-98030527	AG09319	gingival:	n/a
43	chr7:98029285-98029335	HCM	heart:	n/a
44	chr7:98030641-98030691	SK-N-SH	brain:	n/a
45	chr7:98029266-98029316	PANC-1	pancreas:	n/a
46	chr7:98030641-98030691	RPTEC	kidney:	n/a
47	chr7:98030098-98030148	HCF	heart:	n/a
48	chr7:98029285-98029335	PFSK-1	brain:	n/a
49	chr7:98029285-98029335	SKMC	muscle:	n/a
50	chr7:98031846-98031896	HMEC	breast:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:98029240..98030921-chr7:98032784..98035321,2	K562	blood:
2	chr7:97998858..98000704-chr7:98027178..98028821,2	MCF-7	breast:
3	chr7:97923208..97926071-chr7:98023782..98025314,2	K562	blood:
4	chr7:98015865..98017595-chr7:98028896..98031691,2	MCF-7	breast:
5	chr7:98028827..98031634-chr7:98036336..98039927,3	MCF-7	breast:
6	chr7:98040759..98042460-chr7:98475931..98478744,2	K562	blood:
7	chr7:97987419..97989875-chr7:98026560..98028581,2	K562	blood:
8	chr7:98028440..98031404-chr7:98475727..98477431,2	MCF-7	breast:
9	chr7:98013767..98016196-chr7:98019830..98022730,2	K562	blood:
10	chr7:98011872..98013526-chr7:98027965..98030141,2	MCF-7	breast:
11	chr7:98023392..98026419-chr7:98028385..98032176,4	K562	blood:
12	chr7:97880638..97884180-chr7:98029742..98031678,3	MCF-7	breast:
13	chr7:98038571..98040812-chr7:98042172..98044286,2	K562	blood:
14	chr7:98030119..98030807-chr7:104652916..104653616,2	Hela-S3	cervix:
15	chr7:98018093..98019903-chr7:98028373..98029926,2	MCF-7	breast:
16	chr7:97951456..97952264-chr7:98030192..98031073,2	MCF-7	breast:
17	chr7:97501305..97502999-chr7:98028998..98030520,2	K562	blood:
18	chr7:98015865..98017595-chr7:98028896..98031691,2	MCF-7	breast:
19	chr7:97948846..97953573-chr7:98026962..98031463,6	MCF-7	breast:
20	chr7:98030340..98032059-chr7:98040781..98043607,2	MCF-7	breast:
21	chr7:98023705..98027880-chr7:98028270..98031310,4	MCF-7	breast:
22	chr7:98023816..98025610-chr7:98048649..98050466,2	MCF-7	breast:
23	chr7:97948534..97953392-chr7:98027922..98031084,5	MCF-7	breast:
24	chr7:98028301..98030360-chr7:98475060..98477669,2	K562	blood:
25	chr7:97951366..97952341-chr7:98030179..98031154,3	MCF-7	breast:
26	chr7:98023392..98027153-chr7:98028051..98031906,5	K562	blood:
27	chr7:97851992..97854043-chr7:98027877..98030619,2	K562	blood:
28	chr7:98033453..98035045-chr7:98047137..98049429,2	MCF-7	breast:

No data

Variant related genes	Relation type
BAIAP2L1	TF binding region
RPS3AP26	TF binding region
BAIAP2L1	CpG island
RPS3AP26	CpG island
ENSG00000070669	chromatin interactions
ENSG00000272950	chromatin interactions
ENSG00000006453	chromatin interactions
ENSG00000228393	chromatin interactions
ENSG00000214389	chromatin interactions
ENSG00000196367	chromatin interactions
ENSG00000205356	chromatin interactions
ENSG00000164713	chromatin interactions

Extended variants
information (count: 1229 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1229 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548869195	chr7:98013508-98013509	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs565202418	chr7:98013514-98013515	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs560586688	chr7:98013522-98013523	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs547691257	chr7:98013536-98013537	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs566123835	chr7:98013561-98013562	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs142187514	chr7:98013563-98013564	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs190620697	chr7:98013602-98013603	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs373454257	chr7:98013629-98013630	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs146351263	chr7:98013678-98013679	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs537671702	chr7:98013712-98013713	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs7788825	chr7:98013768-98013769	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs12539761	chr7:98013839-98013840	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs577347964	chr7:98013851-98013852	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs369572803	chr7:98013870-98013871	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs139761617	chr7:98013911-98013912	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs11413562	chr7:98014005-98014006	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs146074730	chr7:98014026-98014027	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs11772432	chr7:98014041-98014042	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs537950026	chr7:98014054-98014055	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs571718812	chr7:98014074-98014075	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs542171561	chr7:98014080-98014081	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs111749432	chr7:98014084-98014085	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs533739612	chr7:98014093-98014094	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs576024514	chr7:98014095-98014096	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs144451397	chr7:98014106-98014107	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs564959306	chr7:98014113-98014114	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs532328645	chr7:98014116-98014117	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs58891376	chr7:98014122-98014123	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs2394853	chr7:98014127-98014128	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs60608546	chr7:98014136-98014137	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs541375329	chr7:98014164-98014165	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs559645947	chr7:98014167-98014168	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs148411535	chr7:98014185-98014186	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs548572905	chr7:98014212-98014213	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs570148452	chr7:98014239-98014240	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs530937323	chr7:98014279-98014280	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs183133395	chr7:98014316-98014317	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs570998813	chr7:98014317-98014318	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs549970646	chr7:98014331-98014332	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs373065405	chr7:98014334-98014335	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs574618503	chr7:98014336-98014337	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs533834879	chr7:98014340-98014341	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs568389445	chr7:98014346-98014347	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs535863452	chr7:98014349-98014350	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs187121743	chr7:98014430-98014431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs575968778	chr7:98014432-98014433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs6960566	chr7:98014448-98014449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs112675086	chr7:98014464-98014465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs376424013	chr7:98014525-98014526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs558608613	chr7:98014528-98014529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
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
Cancer	20164920	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bladder cancer	21909424	CNVD
Acute lymphoblastic leukemia	21339820	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
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:687 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:97990400-98017200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr7:97990400-98028000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr7:97992000-98029400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr7:97992800-98017400	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr7:97995800-98028200	Weak transcription	Esophagus	oesophagus
6	chr7:98002600-98027600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr7:98003000-98021600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr7:98003000-98023600	Weak transcription	Hela-S3	cervix
9	chr7:98003400-98016600	Weak transcription	NHEK	skin
10	chr7:98004000-98017200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr7:98005800-98018400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr7:98007400-98016600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr7:98007400-98028000	Weak transcription	Fetal Stomach	stomach
14	chr7:98007800-98018400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr7:98008200-98014200	Weak transcription	Lung	lung
16	chr7:98008800-98014000	Weak transcription	Pancreas	Pancrea
17	chr7:98009800-98017800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr7:98010200-98013600	Enhancers	Rectal Mucosa Donor 31	rectum
19	chr7:98010400-98016200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr7:98010400-98021200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr7:98010800-98015400	Weak transcription	HMEC	breast
22	chr7:98011000-98014000	Weak transcription	Gastric	stomach
23	chr7:98011000-98014800	Weak transcription	Colonic Mucosa	Colon
24	chr7:98011000-98014800	Enhancers	Fetal Intestine Small	intestine
25	chr7:98011000-98016200	Weak transcription	Fetal Muscle Leg	muscle
26	chr7:98011000-98016400	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr7:98011000-98016400	Weak transcription	A549	lung
28	chr7:98011200-98020800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
29	chr7:98011200-98021000	Weak transcription	GM12878-XiMat	blood
30	chr7:98011200-98021200	Weak transcription	HepG2	liver
31	chr7:98011600-98016400	Weak transcription	Fetal Muscle Trunk	muscle
32	chr7:98011800-98016200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr7:98013000-98013600	Weak transcription	Fetal Intestine Large	intestine
34	chr7:98013000-98015000	Enhancers	Liver	Liver
35	chr7:98013200-98016400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr7:98013400-98013800	Weak transcription	Stomach Mucosa	stomach
37	chr7:98013400-98014000	Active TSS	Duodenum Mucosa	Duodenum
38	chr7:98013400-98014000	Enhancers	Pancreatic Islets	Pancreatic Islet
39	chr7:98013400-98014000	Active TSS	Rectal Mucosa Donor 29	rectum
40	chr7:98013600-98014000	Active TSS	Rectal Mucosa Donor 31	rectum
41	chr7:98013600-98014600	Enhancers	Fetal Intestine Large	intestine
42	chr7:98013600-98023600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr7:98013800-98015200	Enhancers	Stomach Mucosa	stomach
44	chr7:98014000-98014200	Flanking Active TSS	Duodenum Mucosa	Duodenum
45	chr7:98014000-98014400	Enhancers	Gastric	stomach
46	chr7:98014000-98014400	Enhancers	Pancreas	Pancrea
47	chr7:98014000-98014400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
48	chr7:98014000-98014400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
49	chr7:98014200-98014600	Enhancers	Duodenum Mucosa	Duodenum
50	chr7:98014200-98014600	Enhancers	Lung	lung

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