Variant report

Variant	nsv5708
Chromosome Location	chr7:39814330-39855535
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:536)
CpG islands
(count:489)
Chromatin interactive
region (count:7)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:536 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:39849823-39850155	K562	blood:	n/a	n/a
2	ARID3A	chr7:39850954-39851273	K562	blood:	n/a	n/a
3	ATF1	chr7:39849719-39850193	K562	blood:	n/a	n/a
4	ATF3	chr7:39849876-39850034	K562	blood:	n/a	n/a
5	ATF3	chr7:39849753-39850225	K562	blood:	n/a	n/a
6	BATF	chr7:39826291-39826499	GM12878	blood:	n/a	n/a
7	BATF	chr7:39826290-39826567	GM12878	blood:	n/a	n/a
8	BCL3	chr7:39849695-39850169	K562	blood:	n/a	n/a
9	BCLAF1	chr7:39849671-39850246	K562	blood:	n/a	chr7:39849683-39849692
10	BCLAF1	chr7:39849788-39850204	K562	blood:	n/a	n/a
11	BHLHE40	chr7:39849789-39850210	K562	blood:	n/a	n/a
12	BHLHE40	chr7:39837834-39837963	K562	blood:	n/a	n/a
13	BHLHE40	chr7:39837820-39837975	HepG2	liver:	n/a	n/a
14	CBX3	chr7:39849669-39850317	K562	blood:	n/a	n/a
15	CBX3	chr7:39849736-39850145	K562	blood:	n/a	n/a
16	CBX3	chr7:39831433-39831839	K562	blood:	n/a	n/a
17	CBX3	chr7:39836592-39836899	K562	blood:	n/a	n/a
18	CCNT2	chr7:39850960-39851275	K562	blood:	n/a	n/a
19	CCNT2	chr7:39849685-39850235	K562	blood:	n/a	n/a
20	CEBPB	chr7:39851095-39851364	K562	blood:	n/a	n/a
21	CEBPB	chr7:39852929-39853086	K562	blood:	n/a	n/a
22	CEBPB	chr7:39853010-39853058	HepG2	liver:	n/a	n/a
23	CEBPB	chr7:39825939-39826087	HepG2	liver:	n/a	chr7:39826051-39826062
24	CEBPB	chr7:39849860-39850321	MCF-7	breast:	n/a	n/a
25	CEBPB	chr7:39816708-39817032	K562	blood:	n/a	chr7:39816882-39816893
26	CEBPB	chr7:39851884-39851983	HepG2	liver:	n/a	chr7:39851930-39851941
27	CEBPB	chr7:39825964-39826087	K562	blood:	n/a	chr7:39826051-39826062
28	CEBPB	chr7:39816765-39817021	IMR90	lung:	n/a	chr7:39816882-39816893
29	CEBPB	chr7:39851907-39852065	K562	blood:	n/a	chr7:39851930-39851941
30	CEBPB	chr7:39849825-39850261	K562	blood:	n/a	n/a
31	CEBPB	chr7:39849754-39850271	K562	blood:	n/a	n/a
32	CEBPB	chr7:39825902-39826102	IMR90	lung:	n/a	chr7:39826051-39826062
33	CEBPB	chr7:39816783-39817025	A549	lung:	n/a	chr7:39816882-39816893
34	CEBPB	chr7:39849914-39850125	K562	blood:	n/a	n/a
35	CEBPB	chr7:39839062-39839260	K562	blood:	n/a	n/a
36	CEBPB	chr7:39816708-39817080	HepG2	liver:	n/a	chr7:39816882-39816893
37	CEBPB	chr7:39821141-39821517	IMR90	lung:	n/a	n/a
38	CEBPD	chr7:39849639-39850311	K562	blood:	n/a	n/a
39	CEBPD	chr7:39849650-39850233	K562	blood:	n/a	n/a
40	CHD2	chr7:39849803-39850213	K562	blood:	n/a	n/a
41	CREB1	chr7:39849720-39850222	K562	blood:	n/a	n/a
42	CREB1	chr7:39849659-39850312	K562	blood:	n/a	n/a
43	CTCF	chr7:39831583-39831812	MCF-7	breast:	n/a	n/a
44	CTCF	chr7:39831612-39831776	A549	lung:	n/a	n/a
45	CTCF	chr7:39849980-39850130	NHEK	skin:	n/a	chr7:39850087-39850105
46	CTCF	chr7:39831620-39831770	GM12874	blood:	n/a	n/a
47	CTCF	chr7:39843761-39844099	A549	lung:	n/a	n/a
48	CTCF	chr7:39831540-39831790	HCT-116	colon:	n/a	n/a
49	CTCF	chr7:39831600-39831750	GM12871	blood:	n/a	n/a
50	CTCF	chr7:39831631-39831779	GM19240	blood:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:39832738-39832788	BE2_C	brain:	n/a
2	chr7:39832738-39832788	BE2_C	brain:	n/a
3	chr7:39831928-39831978	GM19239	blood:	n/a
4	chr7:39833648-39833698	A549	lung:	n/a
5	chr7:39833648-39833698	T-47D	breast:	n/a
6	chr7:39831642-39831692	LNCaP	prostate:	n/a
7	chr7:39833944-39833994	U87	brain:	n/a
8	chr7:39831642-39831692	GM19239	blood:	n/a
9	chr7:39833628-39833678	GM06990	blood:	n/a
10	chr7:39832738-39832788	SKMC	muscle:	n/a
11	chr7:39833648-39833698	Jurkat	blood:	n/a
12	chr7:39833495-39833545	RPTEC	kidney:	n/a
13	chr7:39833944-39833994	AG04450	lung:	fetal
14	chr7:39833495-39833545	NH-A	brain:	n/a
15	chr7:39831928-39831978	AG09309	skin:	n/a
16	chr7:39833944-39833994	Hepatocyte	liver:	n/a
17	chr7:39831928-39831978	ProgFib	skin:	n/a
18	chr7:39833648-39833698	K562	blood:	n/a
19	chr7:39833648-39833698	U87	brain:	n/a
20	chr7:39833648-39833698	ProgFib	skin:	n/a
21	chr7:39837692-39837742	NHDF-neo	bronchial:	n/a
22	chr7:39833648-39833698	HCM	heart:	n/a
23	chr7:39831928-39831978	NB4	blood:	n/a
24	chr7:39833648-39833698	HPAEpiC	pulmonary alveolar:	n/a
25	chr7:39832738-39832788	GM12892	blood:	n/a
26	chr7:39833628-39833678	Hepatocyte	liver:	n/a
27	chr7:39833495-39833545	U87	brain:	n/a
28	chr7:39831928-39831978	HepG2	liver:	n/a
29	chr7:39831642-39831692	HAEpiC	amniotic membrane:	n/a
30	chr7:39833648-39833698	LNCaP	prostate:	n/a
31	chr7:39833944-39833994	H1-hESC	embryonic stem cell:	embryo
32	chr7:39833648-39833698	AG10803	skin:	n/a
33	chr7:39833495-39833545	K562	blood:	n/a
34	chr7:39832738-39832788	T-47D	breast:	n/a
35	chr7:39831928-39831978	RPTEC	kidney:	n/a
36	chr7:39831928-39831978	HRPEpiC	eye:	n/a
37	chr7:39833648-39833698	GM19239	blood:	n/a
38	chr7:39837692-39837742	AG04449	skin:	fetal
39	chr7:39837692-39837742	SKMC	muscle:	n/a
40	chr7:39833495-39833545	HCPEpiC	choroid plexus:	n/a
41	chr7:39833944-39833994	SKMC	muscle:	n/a
42	chr7:39831928-39831978	SK-N-MC	brain:	n/a
43	chr7:39837692-39837742	IMR90	lung:	fetal
44	chr7:39833648-39833698	BE2_C	brain:	n/a
45	chr7:39832738-39832788	NT2-D1	testis:	n/a
46	chr7:39833944-39833994	NT2-D1	testis:	n/a
47	chr7:39833495-39833545	ProgFib	skin:	n/a
48	chr7:39831928-39831978	PANC-1	pancreas:	n/a
49	chr7:39831928-39831978	HRE	kidney:	n/a
50	chr7:39831928-39831978	SK-N-SH	brain:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:39847752..39849916-chr7:39989058..39991146,2	K562	blood:
2	chr7:39453463..39455969-chr7:39846035..39848815,2	K562	blood:
3	chr7:39619917..39620450-chr7:39831240..39831746,2	K562	blood:
4	chr7:39850013..39852934-chr7:39855133..39858067,2	MCF-7	breast:
5	chr7:39849762..39852736-chr7:39853685..39855413,2	K562	blood:
6	chr7:39849762..39852736-chr7:39853685..39855413,2	K562	blood:
7	chr7:39847399..39849610-chr7:40172983..40175978,2	K562	blood:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RALA-1	chr7:39822334-39822398	ENSG00000188185
2	lnc-RALA-1	chr7:39822334-39822346	NONHSAT120225
3	lnc-RALA-1	chr7:39822334-39822369	XLOC_006058
4	lnc-RALA-1	chr7:39828081-39828203	ENSG00000188185
5	lnc-RALA-1	chr7:39822334-39822369	XLOC_006058
6	lnc-RALA-1	chr7:39821706-39821711	XLOC_006058
7	lnc-RALA-1	chr7:39820783-39821484	XLOC_006058
8	lnc-RALA-1	chr7:39828953-39829024	ENSG00000188185
9	lnc-RALA-1	chr7:39820934-39820950	XLOC_006058
10	lnc-RALA-1	chr7:39821161-39821495	XLOC_006058
11	lnc-RALA-1	chr7:39818870-39819091	XLOC_006057
12	lnc-RALA-1	chr7:39820742-39821484	NONHSAT120225
13	lnc-RALA-1	chr7:39821343-39821627	XLOC_006058
14	lnc-RALA-1	chr7:39821161-39821484	XLOC_006058
15	lnc-C7orf11-12	chr7:39828566-39828903	NONHSAT120229
16	lnc-RALA-1	chr7:39821288-39821495	ENSG00000188185

No data

Variant related genes	Relation type
ENSG00000270797	TF binding region
LINC00265	TF binding region
ENSG00000237251	TF binding region
CICP22	TF binding region
ENSG00000270797	CpG island
LINC00265	CpG island
ENSG00000237251	CpG island
CICP22	CpG island
ENSG00000175600	chromatin interactions
ENSG00000237251	chromatin interactions
ENSG00000065883	chromatin interactions
ENSG00000168303	chromatin interactions
ENSG00000259826	chromatin interactions
CRK	miRNA target sites
ZMYND11	miRNA target sites
TMED10	miRNA target sites
SMARCD1	miRNA target sites

Extended variants
information (count: 1708 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1708 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376125115	chr7:39814341-39814342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs539141640	chr7:39814349-39814350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs559143007	chr7:39814351-39814352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs3966602	chr7:39814367-39814368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs4052220	chr7:39814370-39814371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs575700240	chr7:39814386-39814387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs542333721	chr7:39814410-39814411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs140588291	chr7:39814411-39814412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs189601838	chr7:39814437-39814438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs574667375	chr7:39814443-39814444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs9769590	chr7:39814466-39814467	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs62453010	chr7:39814491-39814492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs560098357	chr7:39814507-39814508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs576825792	chr7:39814536-39814537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs545488243	chr7:39814542-39814543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs562281719	chr7:39814575-39814576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs2329510	chr7:39814641-39814642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs2876878	chr7:39814645-39814646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs3040146	chr7:39814648-39814649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs531190169	chr7:39814669-39814670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs547808833	chr7:39814676-39814677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs2329511	chr7:39814690-39814691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs182184464	chr7:39814692-39814693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs185176657	chr7:39814710-39814711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs547127549	chr7:39814718-39814719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs3966603	chr7:39814803-39814804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs566951496	chr7:39814810-39814811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs373099031	chr7:39814821-39814822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs539280162	chr7:39814823-39814824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs190003205	chr7:39814867-39814868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs3966604	chr7:39814878-39814879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs4052221	chr7:39814885-39814886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs142576903	chr7:39814887-39814888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs538215836	chr7:39814913-39814914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs2329512	chr7:39814914-39814915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs4052222	chr7:39814935-39814936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs554679863	chr7:39814939-39814940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs2329513	chr7:39814946-39814947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs2329514	chr7:39814954-39814955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs2876879	chr7:39814963-39814964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs2876880	chr7:39814971-39814972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs565150193	chr7:39814972-39814973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs2876881	chr7:39814973-39814974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs2876882	chr7:39814995-39814996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs2329515	chr7:39815031-39815032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs111441520	chr7:39815037-39815038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs574634588	chr7:39815044-39815045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs145868025	chr7:39815052-39815053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs112058436	chr7:39815061-39815062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs554082342	chr7:39815103-39815104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
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
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
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	17237825	CNVD
Breast cancer	17899364	CNVD
Breast cancer	20409316	CNVD
Acute monocytic leukemia	16498392	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Gastric cancer	24379144	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Bladder cancer	21909424	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:376 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:39776600-39820400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
2	chr7:39785000-39831800	Weak transcription	Primary B cells from cord blood	blood
3	chr7:39794000-39830800	Weak transcription	Pancreas	Pancrea
4	chr7:39794200-39820800	Weak transcription	Ovary	ovary
5	chr7:39794200-39837400	Weak transcription	Stomach Smooth Muscle	stomach
6	chr7:39794600-39830800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr7:39795400-39833400	Weak transcription	Primary T helper cells fromperipheralblood	blood
8	chr7:39798200-39820800	Weak transcription	Esophagus	oesophagus
9	chr7:39798200-39831000	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr7:39798400-39830800	Weak transcription	Fetal Intestine Small	intestine
11	chr7:39799000-39821200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr7:39799800-39820400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr7:39801600-39820800	Weak transcription	Placenta	Placenta
14	chr7:39801600-39831600	Weak transcription	Gastric	stomach
15	chr7:39801600-39833600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr7:39801800-39831000	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr7:39801800-39831400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr7:39802000-39830800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr7:39802000-39835200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr7:39802600-39820200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr7:39802600-39821200	Weak transcription	Adipose Nuclei	Adipose
22	chr7:39802600-39833000	Weak transcription	Dnd41	blood
23	chr7:39802800-39830800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr7:39802800-39835000	Weak transcription	Brain Hippocampus Middle	brain
25	chr7:39803000-39820400	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr7:39803000-39820800	Weak transcription	Fetal Muscle Leg	muscle
27	chr7:39803000-39824400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr7:39803400-39820200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr7:39803400-39832000	Weak transcription	Fetal Thymus	thymus
30	chr7:39803600-39820400	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr7:39805200-39834400	Weak transcription	Duodenum Smooth Muscle	Duodenum
32	chr7:39805400-39821000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
33	chr7:39805400-39831000	Weak transcription	Fetal Brain Female	brain
34	chr7:39805600-39823400	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr7:39806000-39822800	Weak transcription	Primary T helper cells PMA-I stimulated	--
36	chr7:39806200-39820800	Weak transcription	Rectal Mucosa Donor 29	rectum
37	chr7:39806400-39814600	Weak transcription	Fetal Lung	lung
38	chr7:39807400-39830800	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr7:39807800-39820200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr7:39807800-39821200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr7:39807800-39830800	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr7:39807800-39830800	Weak transcription	Brain Cingulate Gyrus	brain
43	chr7:39807800-39830800	Weak transcription	Thymus	Thymus
44	chr7:39807800-39832800	Weak transcription	Brain Anterior Caudate	brain
45	chr7:39808200-39833000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr7:39808200-39833800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr7:39808400-39832800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr7:39808400-39833200	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr7:39808600-39820400	Weak transcription	Primary T cells fromperipheralblood	blood
50	chr7:39809400-39830800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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