Variant report

Variant	nsv970560
Chromosome Location	chr7:99821528-99832022
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:207)
CpG islands
(count:0)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:207 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:99824274-99824474	K562	blood:	n/a	n/a
2	BHLHE40	chr7:99824184-99824442	K562	blood:	n/a	n/a
3	CBX3	chr7:99824125-99824838	K562	blood:	n/a	n/a
4	CBX3	chr7:99828890-99829324	K562	blood:	n/a	n/a
5	CEBPD	chr7:99824274-99824532	K562	blood:	n/a	n/a
6	CTCF	chr7:99824380-99824530	HCPEpiC	choroid plexus:	n/a	n/a
7	CTCF	chr7:99824200-99824350	HCPEpiC	choroid plexus:	n/a	n/a
8	CTCF	chr7:99824110-99824810	K562	blood:	n/a	chr7:99824634-99824647 chr7:99824590-99824603
9	CTCF	chr7:99831027-99831136	Hela-S3	cervix:	n/a	n/a
10	CTCF	chr7:99824440-99824590	SK-N-SH_RA	brain:	n/a	n/a
11	CTCF	chr7:99831020-99831170	MCF-7	breast:	n/a	n/a
12	CTCF	chr7:99824380-99824530	WERI-Rb-1	eye:	n/a	n/a
13	CTCF	chr7:99824300-99824450	SAEC	small airway:	n/a	n/a
14	CTCF	chr7:99824164-99824637	K562	blood:	n/a	chr7:99824590-99824603
15	CTCF	chr7:99831057-99831121	HepG2	liver:	n/a	n/a
16	CTCF	chr7:99831015-99831158	HepG2	liver:	n/a	n/a
17	CTCF	chr7:99824294-99824587	K562	blood:	n/a	n/a
18	CTCF	chr7:99824460-99824610	HCM	heart:	n/a	chr7:99824590-99824603
19	CTCF	chr7:99830202-99830220	GM13976	blood:	n/a	n/a
20	CTCF	chr7:99824439-99824544	K562	blood:	n/a	n/a
21	CTCF	chr7:99824438-99824525	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr7:99824300-99824579	K562	blood:	n/a	n/a
23	CTCF	chr7:99824330-99824620	H1-hESC	embryonic stem cell:	n/a	chr7:99824590-99824603
24	E2F6	chr7:99824220-99824418	K562	blood:	n/a	n/a
25	ELF1	chr7:99824181-99824569	K562	blood:	n/a	n/a
26	ELF1	chr7:99824181-99824540	K562	blood:	n/a	n/a
27	EP300	chr7:99824268-99824526	K562	blood:	n/a	n/a
28	GATA2	chr7:99824091-99824617	K562	blood:	n/a	n/a
29	HEY1	chr7:99824244-99824647	K562	blood:	n/a	n/a
30	HEY1	chr7:99824303-99824544	K562	blood:	n/a	n/a
31	HMGN3	chr7:99824434-99824613	K562	blood:	n/a	n/a
32	IRF1	chr7:99824284-99824479	K562	blood:	n/a	n/a
33	JUND	chr7:99824178-99824481	K562	blood:	n/a	n/a
34	MAX	chr7:99824174-99824612	K562	blood:	n/a	n/a
35	MAX	chr7:99824363-99824534	K562	blood:	n/a	n/a
36	MAX	chr7:99828912-99829297	K562	blood:	n/a	n/a
37	MAZ	chr7:99824186-99824549	K562	blood:	n/a	n/a
38	MTA3	chr7:99831447-99832075	GM12878	blood:	n/a	n/a
39	MTA3	chr7:99822333-99822789	GM12878	blood:	n/a	n/a
40	MTA3	chr7:99828890-99829249	GM12878	blood:	n/a	n/a
41	MTA3	chr7:99824398-99824721	GM12878	blood:	n/a	n/a
42	MTA3	chr7:99825962-99826486	GM12878	blood:	n/a	n/a
43	MTA3	chr7:99823507-99824354	GM12878	blood:	n/a	n/a
44	MYC	chr7:99824410-99824461	K562	blood:	n/a	n/a
45	NFATC1	chr7:99825406-99825744	GM12878	blood:	n/a	n/a
46	NFATC1	chr7:99824976-99825247	GM12878	blood:	n/a	n/a
47	NFATC1	chr7:99831802-99832683	GM12878	blood:	n/a	n/a
48	NFYA	chr7:99824109-99824232	K562	blood:	n/a	n/a
49	NFYB	chr7:99824034-99824316	K562	blood:	n/a	chr7:99824219-99824234 chr7:99824219-99824234
50	NR2F2	chr7:99824019-99824842	K562	blood:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:99816172..99818771-chr7:99820736..99823098,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000222482	TF binding region
ENSG00000239521	TF binding region
ENSG00000222482	chromatin interactions
ENSG00000213413	chromatin interactions

Extended variants
information (count: 345 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:345 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555522877	chr7:99821533-99821534	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs375395151	chr7:99821541-99821542	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs369983684	chr7:99821543-99821544	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs200612169	chr7:99821544-99821545	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs185550112	chr7:99821571-99821572	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs546278079	chr7:99821572-99821573	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs199987021	chr7:99821592-99821593	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs369353023	chr7:99821603-99821604	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs372924600	chr7:99821615-99821616	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs376368839	chr7:99821629-99821630	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs568351142	chr7:99821630-99821631	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs201066587	chr7:99821631-99821632	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs535632275	chr7:99821633-99821634	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs557105539	chr7:99821634-99821635	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs192797829	chr7:99821667-99821668	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs201151121	chr7:99821668-99821669	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs863450	chr7:99821685-99821686	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs377722527	chr7:99821707-99821708	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs117078557	chr7:99821725-99821726	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
20	rs201579733	chr7:99821726-99821727	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs540773230	chr7:99821778-99821779	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs182615311	chr7:99821779-99821780	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs77890086	chr7:99821838-99821839	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs372167927	chr7:99821839-99821840	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs79943159	chr7:99821854-99821855	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs386410818	chr7:99821859-99821860	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs10673922	chr7:99821860-99821861	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs858510	chr7:99821894-99821895	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs527340927	chr7:99821938-99821939	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs542058555	chr7:99821967-99821968	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs563455890	chr7:99821991-99821992	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs112937896	chr7:99822002-99822003	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs139202020	chr7:99822032-99822033	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs11762063	chr7:99822056-99822057	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs546075256	chr7:99822070-99822071	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs563964671	chr7:99822094-99822095	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs372223851	chr7:99822122-99822123	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs528062422	chr7:99822164-99822165	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs546318618	chr7:99822179-99822180	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs188082461	chr7:99822207-99822208	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs541231161	chr7:99822217-99822218	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs191780932	chr7:99822266-99822267	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs143330194	chr7:99822269-99822270	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs147528467	chr7:99822300-99822301	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs564247533	chr7:99822313-99822314	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs184226498	chr7:99822388-99822389	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs558419961	chr7:99822422-99822423	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs566777842	chr7:99822482-99822483	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs534205334	chr7:99822500-99822501	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs555761097	chr7:99822514-99822515	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
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
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99801400-99826000	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr7:99807200-99828400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr7:99807200-99847000	Weak transcription	Fetal Kidney	kidney
4	chr7:99809200-99834800	Weak transcription	HSMMtube	muscle
5	chr7:99810600-99864000	Weak transcription	Right Atrium	heart
6	chr7:99811400-99828600	Weak transcription	HepG2	liver
7	chr7:99811600-99823800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr7:99811600-99834800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr7:99812200-99823800	Weak transcription	Stomach Mucosa	stomach
10	chr7:99812400-99839600	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr7:99813800-99825000	Weak transcription	Psoas Muscle	Psoas
12	chr7:99813800-99829400	Weak transcription	Colon Smooth Muscle	Colon
13	chr7:99813800-99838800	Weak transcription	Fetal Brain Male	brain
14	chr7:99813800-99841200	Weak transcription	Left Ventricle	heart
15	chr7:99813800-99846800	Weak transcription	Ovary	ovary
16	chr7:99815000-99828200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
17	chr7:99815200-99828800	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr7:99815400-99825600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr7:99815400-99834800	Weak transcription	A549	lung
20	chr7:99815400-99834800	Weak transcription	Osteobl	bone
21	chr7:99815600-99835200	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr7:99815600-99844800	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr7:99815800-99839600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr7:99816400-99823000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr7:99816600-99826400	Strong transcription	Fetal Brain Female	brain
26	chr7:99816600-99827600	Weak transcription	Aorta	Aorta
27	chr7:99816800-99822000	Strong transcription	Brain Angular Gyrus	brain
28	chr7:99816800-99822000	Strong transcription	Brain Substantia Nigra	brain
29	chr7:99816800-99822200	Strong transcription	Brain Hippocampus Middle	brain
30	chr7:99816800-99822600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr7:99816800-99823200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
32	chr7:99816800-99823200	Strong transcription	Brain Cingulate Gyrus	brain
33	chr7:99816800-99823600	Strong transcription	Fetal Stomach	stomach
34	chr7:99816800-99824800	Strong transcription	Brain Germinal Matrix	brain
35	chr7:99816800-99825200	Strong transcription	Brain Inferior Temporal Lobe	brain
36	chr7:99816800-99832000	Strong transcription	Fetal Intestine Small	intestine
37	chr7:99817000-99821600	Strong transcription	Lung	lung
38	chr7:99817000-99824200	Strong transcription	Cortex derived primary cultured neurospheres	brain
39	chr7:99817000-99824200	Strong transcription	Fetal Muscle Trunk	muscle
40	chr7:99817400-99822600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr7:99817400-99822600	Strong transcription	Pancreas	Pancrea
42	chr7:99817600-99821800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr7:99817600-99822600	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
44	chr7:99818000-99821600	Strong transcription	Brain Anterior Caudate	brain
45	chr7:99818000-99830400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr7:99818200-99821800	Strong transcription	Adipose Nuclei	Adipose
47	chr7:99818200-99822000	Transcr. at gene 5' and 3'	Fetal Thymus	thymus
48	chr7:99818200-99822000	Strong transcription	Skeletal Muscle Female	skeletal muscle
49	chr7:99818400-99821800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr7:99818400-99822600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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