Variant report

Variant	nsv1031339
Chromosome Location	chr7:6990866-7098418
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:989)
CpG islands
(count:794)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:989 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:7035158-7035426	K562	blood:	n/a	n/a
2	ARID3A	chr7:7057749-7057838	K562	blood:	n/a	n/a
3	ARID3A	chr7:7082264-7082356	K562	blood:	n/a	n/a
4	ATF1	chr7:7035234-7035465	K562	blood:	n/a	n/a
5	ATF1	chr7:7030191-7030411	K562	blood:	n/a	n/a
6	ATF1	chr7:7087921-7088178	K562	blood:	n/a	n/a
7	ATF1	chr7:6995667-6996128	K562	blood:	n/a	n/a
8	ATF1	chr7:7082150-7082478	K562	blood:	n/a	n/a
9	BACH1	chr7:7030692-7031091	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr7:7026562-7026953	GM12878	blood:	n/a	n/a
11	BATF	chr7:6993800-6993986	GM12878	blood:	n/a	n/a
12	BATF	chr7:7036191-7036435	GM12878	blood:	n/a	n/a
13	BATF	chr7:7030120-7030540	GM12878	blood:	n/a	n/a
14	BATF	chr7:7026518-7026935	GM12878	blood:	n/a	n/a
15	BATF	chr7:7030101-7030522	GM12878	blood:	n/a	n/a
16	BATF	chr7:6992805-6993006	GM12878	blood:	n/a	n/a
17	BATF	chr7:7004618-7004964	GM12878	blood:	n/a	n/a
18	BCL11A	chr7:7026555-7026940	GM12878	blood:	n/a	n/a
19	BCL11A	chr7:7023396-7023703	GM12878	blood:	n/a	n/a
20	BCL11A	chr7:7030165-7030615	GM12878	blood:	n/a	n/a
21	BCL11A	chr7:7026425-7027000	GM12878	blood:	n/a	chr7:7026960-7026969
22	BCL11A	chr7:7030103-7030575	GM12878	blood:	n/a	n/a
23	BCL11A	chr7:7004553-7004898	GM12878	blood:	n/a	n/a
24	BHLHE40	chr7:7030675-7031050	K562	blood:	n/a	n/a
25	BHLHE40	chr7:7026567-7026738	GM12878	blood:	n/a	n/a
26	BHLHE40	chr7:7030667-7031069	GM12878	blood:	n/a	n/a
27	BHLHE40	chr7:6995939-6996011	K562	blood:	n/a	n/a
28	BHLHE40	chr7:7030675-7031056	HepG2	liver:	n/a	n/a
29	BHLHE40	chr7:7030288-7030351	GM12878	blood:	n/a	n/a
30	BHLHE40	chr7:7082156-7082340	K562	blood:	n/a	n/a
31	CBX3	chr7:7038679-7039319	K562	blood:	n/a	n/a
32	CBX3	chr7:7081926-7082829	K562	blood:	n/a	n/a
33	CBX3	chr7:6995674-6996047	K562	blood:	n/a	n/a
34	CBX3	chr7:7035202-7035848	K562	blood:	n/a	n/a
35	CBX3	chr7:7038631-7039377	K562	blood:	n/a	n/a
36	CBX3	chr7:7030732-7031655	K562	blood:	n/a	n/a
37	CCNT2	chr7:7082170-7082395	K562	blood:	n/a	n/a
38	CEBPB	chr7:7057458-7057830	MCF-7	breast:	n/a	n/a
39	CEBPB	chr7:7004784-7004979	K562	blood:	n/a	n/a
40	CEBPB	chr7:7035031-7035787	K562	blood:	n/a	n/a
41	CEBPB	chr7:7073879-7074082	Hela-S3	cervix:	n/a	chr7:7073937-7073948
42	CEBPB	chr7:7002510-7002874	HepG2	liver:	n/a	n/a
43	CEBPB	chr7:7097322-7097542	A549	lung:	n/a	chr7:7097431-7097442
44	CEBPB	chr7:7002619-7002711	IMR90	lung:	n/a	n/a
45	CEBPB	chr7:7057056-7057130	HepG2	liver:	n/a	chr7:7057118-7057129 chr7:7057085-7057096
46	CEBPB	chr7:7097348-7097548	IMR90	lung:	n/a	chr7:7097431-7097442
47	CEBPB	chr7:7035276-7035460	K562	blood:	n/a	n/a
48	CEBPB	chr7:7078904-7079160	HepG2	liver:	n/a	chr7:7078921-7078932 chr7:7079074-7079085 chr7:7078921-7078932
49	CEBPB	chr7:7035274-7035571	K562	blood:	n/a	n/a
50	CEBPB	chr7:7002622-7002771	MCF-7	breast:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:7031200-7031250	NHDF-neo	bronchial:	n/a
2	chr7:7031200-7031250	NHDF-neo	bronchial:	n/a
3	chr7:7032174-7032224	HRCEpiC	kidney:	n/a
4	chr7:7031200-7031250	SKMC	muscle:	n/a
5	chr7:7031200-7031250	HPAEpiC	pulmonary alveolar:	n/a
6	chr7:7098017-7098067	LNCaP	prostate:	n/a
7	chr7:7034818-7034868	GM19239	blood:	n/a
8	chr7:7015218-7015268	ECC-1	luminal epithelium:	n/a
9	chr7:7097910-7097960	AG04449	skin:	fetal
10	chr7:7034818-7034868	AG04450	lung:	fetal
11	chr7:7032174-7032224	Caco-2	colon:	n/a
12	chr7:7032174-7032224	HUVEC	blood vessel:	n/a
13	chr7:7098017-7098067	AG10803	skin:	n/a
14	chr7:7034818-7034868	SK-N-SH	brain:	n/a
15	chr7:6993393-6993443	CMK	blood:	n/a
16	chr7:7031200-7031250	GM12891	blood:	n/a
17	chr7:7097910-7097960	SK-N-SH_RA	brain:	n/a
18	chr7:7034864-7034914	HAEpiC	amniotic membrane:	n/a
19	chr7:7034864-7034914	HMEC	breast:	n/a
20	chr7:6993393-6993443	PFSK-1	brain:	n/a
21	chr7:7032174-7032224	RPTEC	kidney:	n/a
22	chr7:7034864-7034914	HEK293	kidney:	embryo
23	chr7:7015218-7015268	SAEC	small airway:	n/a
24	chr7:7034759-7034809	CMK	blood:	n/a
25	chr7:7034864-7034914	HRPEpiC	eye:	n/a
26	chr7:7098182-7098232	SAEC	small airway:	n/a
27	chr7:7098182-7098232	HEK293	kidney:	embryo
28	chr7:7032174-7032224	PFSK-1	brain:	n/a
29	chr7:7031200-7031250	ovcar-3	ovarian:	n/a
30	chr7:7097910-7097960	HepG2	liver:	n/a
31	chr7:7032174-7032224	NH-A	brain:	n/a
32	chr7:7032174-7032224	AG09309	skin:	n/a
33	chr7:7034864-7034914	Hela-S3	cervix:	n/a
34	chr7:6993429-6993479	ovcar-3	ovarian:	n/a
35	chr7:7098182-7098232	HRCEpiC	kidney:	n/a
36	chr7:7098182-7098232	NH-A	brain:	n/a
37	chr7:7034864-7034914	AG04449	skin:	fetal
38	chr7:7015218-7015268	HIPEpiC	eye:	n/a
39	chr7:7034864-7034914	HRCEpiC	kidney:	n/a
40	chr7:6993393-6993443	U87	brain:	n/a
41	chr7:7031200-7031250	GM19239	blood:	n/a
42	chr7:6993429-6993479	HRCEpiC	kidney:	n/a
43	chr7:7098182-7098232	HMEC	breast:	n/a
44	chr7:7032174-7032224	K562	blood:	n/a
45	chr7:7098017-7098067	PrEC	prostate:	n/a
46	chr7:7031200-7031250	NHBE	bronchial:	n/a
47	chr7:7015218-7015268	SK-N-MC	brain:	n/a
48	chr7:7031959-7032009	SK-N-SH	brain:	n/a
49	chr7:7097910-7097960	HIPEpiC	eye:	n/a
50	chr7:7034759-7034809	GM19239	blood:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:7053634..7055657-chr7:7056741..7058413,2	MCF-7	breast:
2	chr7:7074211..7076243-chr7:7083711..7086454,2	K562	blood:
3	chr7:7071081..7073048-chr7:7074220..7077008,2	K562	blood:
4	chr7:7039931..7042582-chr7:7043359..7045821,2	K562	blood:
5	chr7:7074211..7076243-chr7:7083711..7086454,2	K562	blood:
6	chr7:7075155..7077103-chr7:7078870..7080838,2	K562	blood:
7	chr7:7039931..7042582-chr7:7043359..7045821,2	K562	blood:
8	chr7:7081880..7084410-chr7:7088797..7091542,2	K562	blood:
9	chr7:7075155..7077103-chr7:7078870..7080838,2	K562	blood:
10	chr7:7082115..7084689-chr7:7085988..7087819,2	K562	blood:
11	chr7:7074008..7077103-chr7:7078870..7082330,3	K562	blood:
12	chr7:7071081..7073048-chr7:7074220..7077008,2	K562	blood:
13	chr7:7053634..7055657-chr7:7056741..7058413,2	MCF-7	breast:
14	chr7:7082115..7084689-chr7:7085988..7087819,2	K562	blood:
15	chr7:7081880..7084410-chr7:7088797..7091542,2	K562	blood:
16	chr7:7084346..7086372-chr7:7102099..7103966,2	K562	blood:
17	chr7:7074008..7077103-chr7:7078870..7082330,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000221011	TF binding region
ENSG00000221011	CpG island

Extended variants
information (count: 4107 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:4107 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560739011	chr7:6990881-6990882	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs368450498	chr7:6990885-6990886	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs144631765	chr7:6990887-6990888	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs6943507	chr7:6990891-6990892	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs78545775	chr7:6990895-6990896	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs564270919	chr7:6990897-6990898	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs148472141	chr7:6990899-6990900	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs6943512	chr7:6990900-6990901	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs147147118	chr7:6990944-6990945	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs551009746	chr7:6990949-6990950	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs78178175	chr7:6990967-6990968	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs74788788	chr7:6990985-6990986	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs62440065	chr7:6991011-6991012	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs201673453	chr7:6991027-6991028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs548157957	chr7:6991039-6991040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs144317900	chr7:6991045-6991046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs534011428	chr7:6991059-6991060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs62440066	chr7:6991079-6991080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs186653724	chr7:6991082-6991083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs150733444	chr7:6991085-6991086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs139908309	chr7:6991088-6991089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs191503955	chr7:6991104-6991105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs574303974	chr7:6991116-6991117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs542529193	chr7:6991120-6991121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs75461587	chr7:6991123-6991124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs572385081	chr7:6991156-6991157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs546037265	chr7:6991160-6991161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs564332204	chr7:6991168-6991169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs76254233	chr7:6991184-6991185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs76130501	chr7:6991193-6991194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs80216480	chr7:6991218-6991219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs368289026	chr7:6991220-6991221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs543506655	chr7:6991235-6991236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs182950813	chr7:6991237-6991238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs4320463	chr7:6991241-6991242	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs547755043	chr7:6991244-6991245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs73676420	chr7:6991264-6991265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566799878	chr7:6991265-6991266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs527581142	chr7:6991291-6991292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs552440741	chr7:6991295-6991296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs149816012	chr7:6991298-6991299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs187954828	chr7:6991326-6991327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs555955727	chr7:6991330-6991331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs62440067	chr7:6991344-6991345	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs77457838	chr7:6991347-6991348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs535136126	chr7:6991355-6991356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs74911955	chr7:6991360-6991361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs76688961	chr7:6991387-6991388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs553352126	chr7:6991389-6991390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs77403302	chr7:6991394-6991395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	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
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	21525872	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:296 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6990200-6991000	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr7:6990600-6992800	Weak transcription	NHEK	skin
3	chr7:6992800-6993000	Enhancers	NHEK	skin
4	chr7:6993000-6993200	Enhancers	Rectal Mucosa Donor 31	rectum
5	chr7:6993000-6993600	Active TSS	Breast Myoepithelial Primary Cells	Breast
6	chr7:6993000-6993600	Flanking Active TSS	NHEK	skin
7	chr7:6993200-6993400	Enhancers	Duodenum Mucosa	Duodenum
8	chr7:6993200-6993600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr7:6993200-6993600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
10	chr7:6993200-6994000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr7:6993200-6994000	Enhancers	HMEC	breast
12	chr7:6993600-6993800	Enhancers	NHEK	skin
13	chr7:6993600-6994200	Enhancers	Rectal Mucosa Donor 31	rectum
14	chr7:6993800-6994000	Enhancers	Stomach Mucosa	stomach
15	chr7:6994200-6994800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr7:6995400-6996600	Enhancers	K562	blood
17	chr7:6995400-6997000	Enhancers	Fetal Lung	lung
18	chr7:6995600-6996000	Enhancers	Fetal Heart	heart
19	chr7:7002600-7002800	Enhancers	HepG2	liver
20	chr7:7002800-7003400	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr7:7017400-7018200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr7:7026000-7026800	Enhancers	K562	blood
23	chr7:7026400-7026800	Enhancers	GM12878-XiMat	blood
24	chr7:7026800-7027800	Weak transcription	K562	blood
25	chr7:7027800-7028000	Enhancers	Fetal Lung	lung
26	chr7:7027800-7028200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr7:7027800-7028600	Enhancers	Fetal Intestine Large	intestine
28	chr7:7027800-7030800	Enhancers	K562	blood
29	chr7:7028000-7030600	Weak transcription	Fetal Lung	lung
30	chr7:7028200-7031000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr7:7028600-7029000	Weak transcription	Fetal Intestine Large	intestine
32	chr7:7028800-7029600	Enhancers	Rectal Mucosa Donor 29	rectum
33	chr7:7029000-7029800	Enhancers	Fetal Intestine Large	intestine
34	chr7:7029400-7029600	Enhancers	Rectal Mucosa Donor 31	rectum
35	chr7:7029400-7030000	Enhancers	HepG2	liver
36	chr7:7029400-7030200	Enhancers	Stomach Mucosa	stomach
37	chr7:7029400-7030400	Enhancers	Fetal Intestine Small	intestine
38	chr7:7029600-7029800	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr7:7029600-7029800	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr7:7029600-7029800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
41	chr7:7029600-7030000	Active TSS	Rectal Mucosa Donor 31	rectum
42	chr7:7029600-7030200	Enhancers	Fetal Heart	heart
43	chr7:7029600-7030400	Enhancers	Duodenum Mucosa	Duodenum
44	chr7:7029600-7031400	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr7:7029600-7031400	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr7:7029800-7030400	Weak transcription	Fetal Intestine Large	intestine
47	chr7:7029800-7030800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
48	chr7:7029800-7032200	Active TSS	Rectal Mucosa Donor 29	rectum
49	chr7:7030000-7030200	Weak transcription	Rectal Mucosa Donor 31	rectum
50	chr7:7030000-7031000	Weak transcription	HepG2	liver

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