Variant report

Variant	nsv971208
Chromosome Location	chr7:98992671-98997201
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:451)
CpG islands
(count:122)
Chromatin interactive
region (count:10)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:451 , 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	ATF2	chr7:98994315-98996128	GM12878	blood:	n/a	n/a
2	ATF2	chr7:98996158-98996950	GM12878	blood:	n/a	n/a
3	BCL3	chr7:98994483-98997722	A549	lung:	n/a	n/a
4	BCL3	chr7:98995540-98997091	GM12878	blood:	n/a	n/a
5	BCL3	chr7:98992972-98993739	A549	lung:	n/a	n/a
6	BCL3	chr7:98997130-98997491	GM12878	blood:	n/a	n/a
7	BCL3	chr7:98994171-98995529	GM12878	blood:	n/a	n/a
8	BCL3	chr7:98994159-98998037	A549	lung:	n/a	chr7:98997835-98997843
9	BCL3	chr7:98993161-98994027	GM12878	blood:	n/a	n/a
10	BCL3	chr7:98992155-98992946	A549	lung:	n/a	n/a
11	BCL3	chr7:98993260-98994046	A549	lung:	n/a	n/a
12	BCLAF1	chr7:98996249-98996874	GM12878	blood:	n/a	n/a
13	BCLAF1	chr7:98997068-98997439	GM12878	blood:	n/a	n/a
14	BCLAF1	chr7:98994292-98995061	GM12878	blood:	n/a	n/a
15	BCLAF1	chr7:98995211-98996173	GM12878	blood:	n/a	n/a
16	BHLHE40	chr7:98994351-98994512	K562	blood:	n/a	n/a
17	BRCA1	chr7:98997161-98997232	HepG2	liver:	n/a	n/a
18	CCNT2	chr7:98994456-98994625	K562	blood:	n/a	n/a
19	CCNT2	chr7:98992424-98992672	K562	blood:	n/a	n/a
20	CHD2	chr7:98993916-98993921	K562	blood:	n/a	n/a
21	CHD2	chr7:98995006-98995412	K562	blood:	n/a	n/a
22	CHD2	chr7:98996738-98996892	Hela-S3	cervix:	n/a	n/a
23	CHD2	chr7:98996528-98996828	K562	blood:	n/a	n/a
24	CHD2	chr7:98995818-98995833	K562	blood:	n/a	n/a
25	CHD2	chr7:98994347-98994543	K562	blood:	n/a	n/a
26	CTCF	chr7:98993200-98993350	HPAF	blood vessel:	n/a	n/a
27	CTCF	chr7:98993160-98993310	GM12873	blood:	n/a	n/a
28	CTCF	chr7:98993276-98993350	Gliobla	brain:	n/a	n/a
29	CTCF	chr7:98993240-98993390	RPTEC	kidney:	n/a	n/a
30	CTCF	chr7:98993270-98993371	MCF-7	breast:	n/a	n/a
31	CTCF	chr7:98993240-98993390	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr7:98993300-98993450	AoAF	blood vessel:	n/a	n/a
33	CTCF	chr7:98993220-98993370	NHEK	skin:	n/a	n/a
34	CTCF	chr7:98993285-98993349	MCF-7	breast:	n/a	n/a
35	CTCF	chr7:98993260-98993410	HBMEC	blood vessel:	n/a	n/a
36	CTCF	chr7:98993220-98993370	AG09319	gingival:	n/a	n/a
37	CTCF	chr7:98993180-98993330	SAEC	small airway:	n/a	n/a
38	CTCF	chr7:98993185-98993447	K562	blood:	n/a	n/a
39	CTCF	chr7:98993220-98993370	HFF-Myc	foreskin:	n/a	n/a
40	CTCF	chr7:98993260-98993410	A549	lung:	n/a	n/a
41	CTCF	chr7:98993240-98993390	NB4	blood:	n/a	n/a
42	CTCF	chr7:98993214-98993460	GM12878	blood:	n/a	n/a
43	CTCF	chr7:98993240-98993390	NHDF-neo	bronchial:	n/a	n/a
44	CTCF	chr7:98993257-98993389	GM19239	blood:	n/a	n/a
45	CTCF	chr7:98993238-98993371	MCF-7	breast:	n/a	n/a
46	CTCF	chr7:98993180-98993330	K562	blood:	n/a	n/a
47	CTCF	chr7:98996428-98996446	GM12891	blood:	n/a	n/a
48	CTCF	chr7:98993260-98993410	GM12866	blood:	n/a	n/a
49	CTCF	chr7:98993300-98993450	HMF	breast:	n/a	n/a
50	CTCF	chr7:98996448-98996456	GM12891	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:98996656-98996706	RPTEC	kidney:	n/a
2	chr7:98993133-98993183	K562	blood:	n/a
3	chr7:98993133-98993183	Hela-S3	cervix:	n/a
4	chr7:98996656-98996706	HEK293	kidney:	embryo
5	chr7:98996656-98996706	AG09309	skin:	n/a
6	chr7:98993133-98993183	BE2_C	brain:	n/a
7	chr7:98996656-98996706	HCM	heart:	n/a
8	chr7:98993133-98993183	GM12878	blood:	n/a
9	chr7:98996656-98996706	HPAEpiC	pulmonary alveolar:	n/a
10	chr7:98996656-98996706	IMR90	lung:	fetal
11	chr7:98996656-98996706	GM12892	blood:	n/a
12	chr7:98993133-98993183	AG09319	gingival:	n/a
13	chr7:98993133-98993183	GM06990	blood:	n/a
14	chr7:98993133-98993183	LNCaP	prostate:	n/a
15	chr7:98993133-98993183	H1-hESC	embryonic stem cell:	embryo
16	chr7:98993133-98993183	HNPCEpiC	eye:	n/a
17	chr7:98993133-98993183	HMEC	breast:	n/a
18	chr7:98993133-98993183	MCF-7	breast:	n/a
19	chr7:98996656-98996706	SK-N-SH_RA	brain:	n/a
20	chr7:98993133-98993183	HEK293	kidney:	embryo
21	chr7:98993133-98993183	SK-N-SH_RA	brain:	n/a
22	chr7:98993133-98993183	U87	brain:	n/a
23	chr7:98996656-98996706	NH-A	brain:	n/a
24	chr7:98993133-98993183	HEEpiC	esophagus:	n/a
25	chr7:98996656-98996706	AG10803	skin:	n/a
26	chr7:98993133-98993183	AG04450	lung:	fetal
27	chr7:98993133-98993183	HRCEpiC	kidney:	n/a
28	chr7:98993133-98993183	HCT-116	colon:	n/a
29	chr7:98996656-98996706	A549	lung:	n/a
30	chr7:98996656-98996706	AoSMC	blood vessel:	n/a
31	chr7:98996656-98996706	HNPCEpiC	eye:	n/a
32	chr7:98996656-98996706	PANC-1	pancreas:	n/a
33	chr7:98993133-98993183	HCPEpiC	choroid plexus:	n/a
34	chr7:98996656-98996706	HRCEpiC	kidney:	n/a
35	chr7:98993133-98993183	PFSK-1	brain:	n/a
36	chr7:98993133-98993183	ProgFib	skin:	n/a
37	chr7:98993133-98993183	HUVEC	blood vessel:	n/a
38	chr7:98993133-98993183	AG09309	skin:	n/a
39	chr7:98996656-98996706	MCF10A-Er-Src	breast:	n/a
40	chr7:98996656-98996706	U87	brain:	n/a
41	chr7:98993133-98993183	NHDF-neo	bronchial:	n/a
42	chr7:98993133-98993183	HCM	heart:	n/a
43	chr7:98996656-98996706	H1-hESC	embryonic stem cell:	embryo
44	chr7:98993133-98993183	GM19239	blood:	n/a
45	chr7:98996656-98996706	HEEpiC	esophagus:	n/a
46	chr7:98993133-98993183	PANC-1	pancreas:	n/a
47	chr7:98993133-98993183	MCF10A-Er-Src	breast:	n/a
48	chr7:98996656-98996706	BJ	skin:	n/a
49	chr7:98996656-98996706	GM06990	blood:	n/a
50	chr7:98993133-98993183	HAEpiC	amniotic membrane:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:98995708..98998425-chr7:98998981..99002328,3	MCF-7	breast:
2	chr7:98970545..98974719-chr7:98992685..98998543,7	MCF-7	breast:
3	chr7:98966757..98974253-chr7:98988800..98995304,7	K562	blood:
4	chr7:98972319..98974314-chr7:98993358..98995077,3	MCF-7	breast:
5	chr7:98988826..98993566-chr7:99002963..99006762,7	MCF-7	breast:
6	chr7:98587958..98590431-chr7:98993222..98994998,2	K562	blood:
7	chr7:98983107..98985699-chr7:98992878..98994475,2	MCF-7	breast:
8	chr7:98979371..98979879-chr7:98993328..98994292,2	MCF-7	breast:
9	chr7:98971244..98973231-chr7:98989224..98993180,5	MCF-7	breast:
10	chr7:98992027..98994559-chr7:99000326..99002906,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARPC1B-2	chr7:98996547-98997308	expReg_chr7_6206_+

No data

Variant related genes	Relation type
PDAP1	TF binding region
PDAP1	CpG island
ENSG00000106244	chromatin interactions
ENSG00000106245	chromatin interactions
ENSG00000130429	chromatin interactions

Extended variants
information (count: 180 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:180 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563294534	chr7:98992674-98992675	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs149137422	chr7:98992703-98992704	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs530470574	chr7:98992729-98992730	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs546085956	chr7:98992759-98992760	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs564214152	chr7:98992803-98992804	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs528333149	chr7:98992809-98992810	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs184637196	chr7:98992817-98992818	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs568247553	chr7:98992833-98992834	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs529359787	chr7:98992835-98992836	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs79185041	chr7:98992900-98992901	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs568917324	chr7:98992911-98992912	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs539409428	chr7:98992960-98992961	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs558470578	chr7:98992961-98992962	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs375464115	chr7:98993037-98993038	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs560322110	chr7:98993103-98993104	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs10277362	chr7:98993112-98993113	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs73711206	chr7:98993114-98993115	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs3180759	chr7:98993167-98993168	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs555666393	chr7:98993187-98993188	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs3179479	chr7:98993193-98993194	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs28460612	chr7:98993205-98993206	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs541948270	chr7:98993210-98993211	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs141293967	chr7:98993236-98993237	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs3180760	chr7:98993325-98993326	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs575349926	chr7:98993338-98993339	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs545478115	chr7:98993345-98993346	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs28558950	chr7:98993354-98993355	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs3180761	chr7:98993365-98993366	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs3201781	chr7:98993413-98993414	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs528358424	chr7:98993453-98993454	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs7457303	chr7:98993510-98993511	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs540483621	chr7:98993519-98993520	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs151295043	chr7:98993526-98993527	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs529010700	chr7:98993564-98993565	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs140638970	chr7:98993565-98993566	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs562635425	chr7:98993570-98993571	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs73148810	chr7:98993575-98993576	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs551465074	chr7:98993593-98993594	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs111567746	chr7:98993721-98993722	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs567188475	chr7:98993743-98993744	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs562117246	chr7:98993748-98993749	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs1044111	chr7:98993760-98993761	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs1044101	chr7:98993782-98993783	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs386716088	chr7:98993797-98993798	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs113520208	chr7:98993820-98993821	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs189504181	chr7:98993865-98993866	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs386716089	chr7:98993867-98993868	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs73711208	chr7:98993868-98993869	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs371219946	chr7:98993903-98993904	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs549537131	chr7:98993927-98993928	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	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
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
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
Breast cancer	21509527	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Pancreatic cancer	17952125	CNVD
Prostate cancer	18632612	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:214 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:98979400-99001800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr7:98980400-99003800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
3	chr7:98980800-99000600	Strong transcription	Dnd41	blood
4	chr7:98981000-98993000	Strong transcription	A549	lung
5	chr7:98985600-99003800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr7:98987000-99004200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr7:98990000-99002800	Strong transcription	GM12878-XiMat	blood
8	chr7:98990200-98994600	Weak transcription	NHDF-Ad	bronchial
9	chr7:98991000-98993200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr7:98991000-98995000	Weak transcription	Aorta	Aorta
11	chr7:98991000-98996200	Strong transcription	Monocytes-CD14+_RO01746	blood
12	chr7:98991000-99001600	Strong transcription	Muscle Satellite Cultured Cells	--
13	chr7:98991000-99001600	Strong transcription	Osteobl	bone
14	chr7:98991000-99002000	Strong transcription	NHEK	skin
15	chr7:98991000-99002600	Strong transcription	Primary monocytes fromperipheralblood	blood
16	chr7:98991000-99002600	Strong transcription	Primary neutrophils fromperipheralblood	blood
17	chr7:98991200-98993800	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr7:98991200-98996400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr7:98991200-98996600	Strong transcription	HSMM	muscle
20	chr7:98991400-98993600	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr7:98991400-98994200	Weak transcription	Ovary	ovary
22	chr7:98991400-98995400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr7:98991400-99001800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr7:98991400-99001800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr7:98991400-99001800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr7:98991400-99002400	Strong transcription	Esophagus	oesophagus
27	chr7:98991400-99002400	Weak transcription	Right Atrium	heart
28	chr7:98991400-99004200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr7:98991600-98993200	Weak transcription	Brain Angular Gyrus	brain
30	chr7:98991600-98993200	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr7:98991600-98993400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr7:98991600-98993800	Strong transcription	Rectal Smooth Muscle	rectum
33	chr7:98991600-98994600	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
34	chr7:98991600-98995400	Strong transcription	NH-A	brain
35	chr7:98991600-98996200	Strong transcription	HMEC	breast
36	chr7:98991600-98996400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr7:98991600-98997200	Weak transcription	Pancreatic Islets	Pancreatic Islet
38	chr7:98991600-98999000	Strong transcription	Primary B cells from cord blood	blood
39	chr7:98991600-99001400	Strong transcription	Placenta	Placenta
40	chr7:98991600-99001600	Strong transcription	Duodenum Smooth Muscle	Duodenum
41	chr7:98991600-99001800	Strong transcription	NHLF	lung
42	chr7:98991600-99002000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr7:98991600-99002000	Strong transcription	Adipose Nuclei	Adipose
44	chr7:98991600-99002400	Strong transcription	Primary T helper cells fromperipheralblood	blood
45	chr7:98991600-99002800	Strong transcription	Sigmoid Colon	Sigmoid Colon
46	chr7:98991600-99003000	Strong transcription	Primary T cells from cord blood	blood
47	chr7:98991600-99003000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr7:98991600-99003400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr7:98991600-99003400	Weak transcription	Stomach Mucosa	stomach
50	chr7:98991600-99003400	Strong transcription	K562	blood

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