Variant report

Variant	nsv981812
Chromosome Location	chr7:86827166-86829678
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:124)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:124 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	HCFC1	chr7:86828483-86828503	K562	blood:	n/a	n/a
2	MTA3	chr7:86828305-86828904	GM12878	blood:	n/a	n/a
3	MTA3	chr7:86829164-86830202	GM12878	blood:	n/a	n/a
4	NFATC1	chr7:86828125-86830150	GM12878	blood:	n/a	n/a
5	NFATC1	chr7:86826873-86827553	GM12878	blood:	n/a	n/a
6	NFATC1	chr7:86827898-86830828	GM12878	blood:	n/a	n/a
7	PML	chr7:86829004-86829962	GM12878	blood:	n/a	chr7:86829625-86829633
8	PML	chr7:86827118-86828988	GM12878	blood:	n/a	n/a
9	POLR2A	chr7:86829171-86829192	MCF-7	breast:	n/a	n/a
10	POLR2A	chr7:86828282-86828289	Hela-S3	cervix:	n/a	n/a
11	POLR2A	chr7:86829207-86829216	MCF-7	breast:	n/a	n/a
12	POLR2A	chr7:86828584-86828829	H1-hESC	embryonic stem cell:	n/a	n/a
13	POLR2A	chr7:86828111-86828971	GM12878	blood:	n/a	n/a
14	POLR2A	chr7:86827144-86827468	GM12891	blood:	n/a	n/a
15	POLR2A	chr7:86828147-86829001	GM12878	blood:	n/a	n/a
16	POLR2A	chr7:86829543-86829611	Hela-S3	cervix:	n/a	n/a
17	POLR2A	chr7:86829313-86830246	K562	blood:	n/a	n/a
18	POLR2A	chr7:86828341-86828935	GM12891	blood:	n/a	n/a
19	POLR2A	chr7:86829051-86829062	HUVEC	blood vessel:	n/a	n/a
20	POLR2A	chr7:86829039-86830155	PFSK-1	brain:	n/a	n/a
21	POLR2A	chr7:86826895-86827624	H1-hESC	embryonic stem cell:	n/a	n/a
22	POLR2A	chr7:86829245-86829316	MCF-7	breast:	n/a	n/a
23	POLR2A	chr7:86827698-86827772	Hela-S3	cervix:	n/a	n/a
24	POLR2A	chr7:86829057-86830376	GM12878	blood:	n/a	n/a
25	POLR2A	chr7:86829045-86830022	K562	blood:	n/a	n/a
26	POLR2A	chr7:86829161-86829916	K562	blood:	n/a	n/a
27	POLR2A	chr7:86829174-86830322	HCT-116	colon:	n/a	n/a
28	POLR2A	chr7:86829090-86830786	SK-N-SH	brain:	n/a	n/a
29	POLR2A	chr7:86828693-86828977	HUVEC	blood vessel:	n/a	n/a
30	POLR2A	chr7:86829095-86829891	GM12891	blood:	n/a	n/a
31	POLR2A	chr7:86828696-86828714	K562	blood:	n/a	n/a
32	POLR2A	chr7:86829218-86830685	A549	lung:	n/a	n/a
33	POLR2A	chr7:86828270-86830908	H1-hESC	embryonic stem cell:	n/a	n/a
34	POLR2A	chr7:86827357-86827840	K562	blood:	n/a	n/a
35	POLR2A	chr7:86829084-86829974	GM12878	blood:	n/a	n/a
36	POLR2A	chr7:86829174-86830143	HepG2	liver:	n/a	n/a
37	POLR2A	chr7:86829205-86829376	Hela-S3	cervix:	n/a	n/a
38	POLR2A	chr7:86828677-86828681	K562	blood:	n/a	n/a
39	POLR2A	chr7:86829415-86829798	K562	blood:	n/a	n/a
40	POLR2A	chr7:86828322-86828989	SK-N-SH	brain:	n/a	n/a
41	POLR2A	chr7:86827396-86827548	HUVEC	blood vessel:	n/a	n/a
42	POLR2A	chr7:86828970-86830333	GM12892	blood:	n/a	n/a
43	POLR2A	chr7:86827029-86827732	PFSK-1	brain:	n/a	n/a
44	POLR2A	chr7:86826090-86827563	GM12892	blood:	n/a	n/a
45	POLR2A	chr7:86828380-86829011	GM12891	blood:	n/a	n/a
46	POLR2A	chr7:86828558-86828628	HUVEC	blood vessel:	n/a	n/a
47	POLR2A	chr7:86828384-86829513	HepG2	liver:	n/a	n/a
48	POLR2A	chr7:86829412-86829870	MCF-7	breast:	n/a	n/a
49	POLR2A	chr7:86829001-86829017	HUVEC	blood vessel:	n/a	n/a
50	POLR2A	chr7:86827917-86832918	GM12878	blood:	n/a	n/a

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:86828530..86830093-chr7:86847651..86850923,3	MCF-7	breast:
2	chr7:86828750..86830318-chr7:86830762..86833577,2	MCF-7	breast:
3	chr7:86829249..86831947-chr7:86848696..86850606,2	MCF-7	breast:
4	chr7:86820172..86822835-chr7:86826143..86828085,2	K562	blood:
5	chr7:86826618..86828739-chr7:86829824..86832016,2	K562	blood:
6	chr7:86813289..86815868-chr7:86827062..86829282,2	K562	blood:
7	chr7:86821386..86824076-chr7:86824725..86827371,3	MCF-7	breast:
8	chr7:86780600..86784245-chr7:86826808..86830083,3	K562	blood:
9	chr7:86826595..86828118-chr7:86848559..86850853,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIAA1324L-3	chr7:86828323-86828373	NONHSAT121820
2	lnc-KIAA1324L-3	chr7:86827544-86828373	NONHSAT121822
3	lnc-KIAA1324L-3	chr7:86828323-86828929	NONHSAT121821
4	lnc-KIAA1324L-3	chr7:86827034-86827361	NONHSAT121820
5	lnc-KIAA1324L-3	chr7:86827299-86827361	NONHSAT121821

No data

Variant related genes	Relation type
TMEM243	TF binding region
ENSG00000135164	chromatin interactions
ENSG00000224046	chromatin interactions
ENSG00000135185	chromatin interactions
ENSG00000200397	chromatin interactions

Extended variants
information (count: 114 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:114 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375910303	chr7:86827178-86827179	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
2	rs141327172	chr7:86827180-86827181	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
3	rs187647988	chr7:86827209-86827210	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
4	rs199725948	chr7:86827230-86827231	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
5	rs542357341	chr7:86827287-86827288	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
6	rs111700668	chr7:86827302-86827303	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
7	rs62486481	chr7:86827313-86827314	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
8	rs376712723	chr7:86827314-86827315	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
9	rs201194367	chr7:86827329-86827330	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
10	rs371594820	chr7:86827352-86827353	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
11	rs374589748	chr7:86827357-86827358	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
12	rs377465214	chr7:86827377-86827378	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs370336373	chr7:86827380-86827381	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs374735589	chr7:86827381-86827382	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs113398152	chr7:86827470-86827471	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs532305537	chr7:86827472-86827473	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs138930758	chr7:86827488-86827489	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs568755756	chr7:86827525-86827526	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs190373387	chr7:86827526-86827527	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs530924705	chr7:86827542-86827543	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs181730476	chr7:86827563-86827564	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
22	rs73208517	chr7:86827567-86827568	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs117986766	chr7:86827611-86827612	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
24	rs185902102	chr7:86827651-86827652	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
25	rs149355204	chr7:86827657-86827658	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
26	rs190360013	chr7:86827660-86827661	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
27	rs535268074	chr7:86827664-86827665	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
28	rs113235617	chr7:86827675-86827676	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
29	rs556893743	chr7:86827693-86827694	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
30	rs181261646	chr7:86827710-86827711	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
31	rs368256554	chr7:86827726-86827727	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
32	rs577512813	chr7:86827731-86827732	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
33	rs112944566	chr7:86827733-86827734	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
34	rs542071059	chr7:86827759-86827760	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
35	rs73208519	chr7:86827760-86827761	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs571642928	chr7:86827768-86827769	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
37	rs572471416	chr7:86827772-86827773	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
38	rs546260999	chr7:86827774-86827775	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
39	rs564178326	chr7:86827792-86827793	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
40	rs144698368	chr7:86827800-86827801	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
41	rs543362726	chr7:86827817-86827818	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
42	rs562451965	chr7:86827820-86827821	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
43	rs138273856	chr7:86827846-86827847	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
44	rs185370637	chr7:86827901-86827902	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
45	rs73208521	chr7:86827942-86827943	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs557354924	chr7:86828002-86828003	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
47	rs552292659	chr7:86828016-86828017	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
48	rs575960943	chr7:86828070-86828071	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
49	rs35727906	chr7:86828123-86828124	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs537843538	chr7:86828133-86828134	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	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
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	16616336	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:199 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:86783000-86834000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:86786600-86828400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr7:86788600-86830400	Strong transcription	HUES64 Cell Line	embryonic stem cell
4	chr7:86788600-86832400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr7:86789000-86832400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr7:86789000-86832400	Strong transcription	Dnd41	blood
7	chr7:86789400-86830800	Strong transcription	Monocytes-CD14+_RO01746	blood
8	chr7:86789600-86832400	Strong transcription	Fetal Thymus	thymus
9	chr7:86789800-86833000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
10	chr7:86791000-86831600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr7:86791200-86829400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
12	chr7:86791400-86830000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr7:86791400-86831800	Strong transcription	HUES48 Cell Line	embryonic stem cell
14	chr7:86791400-86831800	Strong transcription	HUES6 Cell Line	embryonic stem cell
15	chr7:86791600-86830600	Strong transcription	Primary T cells fromperipheralblood	blood
16	chr7:86791600-86830600	Strong transcription	NHDF-Ad	bronchial
17	chr7:86791800-86831000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr7:86792000-86829200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr7:86792400-86827200	Strong transcription	Primary T helper cells fromperipheralblood	blood
20	chr7:86792400-86828600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr7:86792400-86828600	Strong transcription	HUVEC	blood vessel
22	chr7:86792400-86829800	Strong transcription	Primary monocytes fromperipheralblood	blood
23	chr7:86792400-86831600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr7:86792600-86828800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
25	chr7:86792600-86829800	Strong transcription	H1 Cell Line	embryonic stem cell
26	chr7:86792600-86830800	Strong transcription	Primary B cells from cord blood	blood
27	chr7:86792600-86832200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr7:86793400-86833400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr7:86794200-86832200	Strong transcription	Muscle Satellite Cultured Cells	--
30	chr7:86803400-86831400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr7:86804600-86832400	Strong transcription	Rectal Mucosa Donor 31	rectum
32	chr7:86807000-86832200	Strong transcription	HSMM	muscle
33	chr7:86808600-86827800	Strong transcription	Rectal Mucosa Donor 29	rectum
34	chr7:86808600-86828400	Strong transcription	Primary B cells from peripheral blood	blood
35	chr7:86808600-86828800	Strong transcription	Liver	Liver
36	chr7:86808600-86830200	Strong transcription	Primary neutrophils fromperipheralblood	blood
37	chr7:86808800-86827600	Strong transcription	Skeletal Muscle Female	skeletal muscle
38	chr7:86808800-86827800	Strong transcription	Placenta	Placenta
39	chr7:86808800-86829200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr7:86808800-86830600	Strong transcription	Fetal Muscle Trunk	muscle
41	chr7:86809400-86829400	Strong transcription	Fetal Intestine Large	intestine
42	chr7:86810200-86827600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr7:86810200-86829000	Strong transcription	Sigmoid Colon	Sigmoid Colon
44	chr7:86810600-86827600	Strong transcription	Skeletal Muscle Male	skeletal muscle
45	chr7:86810600-86828600	Strong transcription	Adipose Nuclei	Adipose
46	chr7:86810600-86830000	Strong transcription	Fetal Lung	lung
47	chr7:86810600-86832200	Strong transcription	Osteobl	bone
48	chr7:86810800-86827400	Strong transcription	ES-I3 Cell Line	embryonic stem cell
49	chr7:86810800-86828200	Strong transcription	K562	blood
50	chr7:86810800-86830400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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