Variant report

Variant	esv1802195
Chromosome Location	chr7:65886451-65945211
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:425)
CpG islands
(count:427)
Chromatin interactive
region (count:10)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:425 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:65904544-65905227	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:65925846-65926274	K562	blood:	n/a	n/a
3	ARID3A	chr7:65925355-65925383	K562	blood:	n/a	n/a
4	ARID3A	chr7:65924754-65925042	K562	blood:	n/a	n/a
5	ATF1	chr7:65904850-65904981	K562	blood:	n/a	n/a
6	ATF1	chr7:65924122-65924164	K562	blood:	n/a	n/a
7	BATF	chr7:65931161-65931434	GM12878	blood:	n/a	n/a
8	BHLHE40	chr7:65924116-65924275	K562	blood:	n/a	n/a
9	BHLHE40	chr7:65925317-65925485	K562	blood:	n/a	n/a
10	BHLHE40	chr7:65903690-65903961	HepG2	liver:	n/a	n/a
11	BHLHE40	chr7:65924673-65925023	K562	blood:	n/a	n/a
12	CBX3	chr7:65925976-65927020	K562	blood:	n/a	n/a
13	CBX3	chr7:65904776-65905196	K562	blood:	n/a	n/a
14	CBX3	chr7:65926079-65926724	K562	blood:	n/a	n/a
15	CCNT2	chr7:65925862-65926076	K562	blood:	n/a	n/a
16	CEBPB	chr7:65931116-65931295	HepG2	liver:	n/a	n/a
17	CEBPB	chr7:65909027-65909199	IMR90	lung:	n/a	n/a
18	CEBPB	chr7:65904829-65905057	HepG2	liver:	n/a	n/a
19	CEBPB	chr7:65904792-65905165	IMR90	lung:	n/a	n/a
20	CEBPB	chr7:65904816-65905103	K562	blood:	n/a	n/a
21	CEBPB	chr7:65904801-65905155	A549	lung:	n/a	n/a
22	CEBPB	chr7:65896531-65896704	IMR90	lung:	n/a	n/a
23	CEBPB	chr7:65904804-65905147	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr7:65904851-65905062	HepG2	liver:	n/a	n/a
25	CEBPB	chr7:65904722-65905151	K562	blood:	n/a	n/a
26	CEBPB	chr7:65904797-65905170	HepG2	liver:	n/a	n/a
27	CEBPB	chr7:65896613-65896675	K562	blood:	n/a	n/a
28	CEBPB	chr7:65931120-65931354	IMR90	lung:	n/a	n/a
29	CEBPB	chr7:65931272-65931427	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr7:65930093-65930163	A549	lung:	n/a	n/a
31	CEBPB	chr7:65931082-65931474	HepG2	liver:	n/a	n/a
32	CEBPB	chr7:65926045-65926245	K562	blood:	n/a	n/a
33	CEBPB	chr7:65904805-65905162	K562	blood:	n/a	n/a
34	CEBPB	chr7:65896599-65896798	HepG2	liver:	n/a	n/a
35	CEBPD	chr7:65924739-65925552	K562	blood:	n/a	n/a
36	CEBPD	chr7:65925856-65926135	K562	blood:	n/a	n/a
37	CEBPD	chr7:65904830-65905157	K562	blood:	n/a	n/a
38	CEBPD	chr7:65925912-65926221	K562	blood:	n/a	n/a
39	CREB1	chr7:65907284-65907713	HepG2	liver:	n/a	n/a
40	CREB1	chr7:65907414-65907804	HepG2	liver:	n/a	n/a
41	CTCF	chr7:65916834-65916923	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr7:65888861-65888948	HUVEC	blood vessel:	n/a	chr7:65888901-65888919 chr7:65888904-65888917
43	CTCF	chr7:65888893-65888954	GM12891	blood:	n/a	chr7:65888901-65888919 chr7:65888904-65888917
44	CTCF	chr7:65888820-65888970	MCF-7	breast:	n/a	chr7:65888901-65888919 chr7:65888904-65888917
45	CTCF	chr7:65888820-65888970	Caco-2	colon:	n/a	chr7:65888901-65888919 chr7:65888904-65888917
46	CTCF	chr7:65904860-65905010	HVMF	connective:	n/a	n/a
47	CTCF	chr7:65904840-65904990	HEK293	kidney:	n/a	n/a
48	CTCF	chr7:65888800-65888950	A549	lung:	n/a	chr7:65888901-65888919 chr7:65888904-65888917
49	CTCF	chr7:65916760-65916910	GM12873	blood:	n/a	n/a
50	CTCF	chr7:65916820-65916970	HCPEpiC	choroid plexus:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:65940909-65940959	HUVEC	blood vessel:	n/a
2	chr7:65939595-65939645	Jurkat	blood:	n/a
3	chr7:65941812-65941862	PANC-1	pancreas:	n/a
4	chr7:65939507-65939557	CMK	blood:	n/a
5	chr7:65939595-65939645	AG09319	gingival:	n/a
6	chr7:65941812-65941862	Hela-S3	cervix:	n/a
7	chr7:65939595-65939645	HIPEpiC	eye:	n/a
8	chr7:65938820-65938870	SAEC	small airway:	n/a
9	chr7:65940909-65940959	BE2_C	brain:	n/a
10	chr7:65939507-65939557	SAEC	small airway:	n/a
11	chr7:65941812-65941862	GM12891	blood:	n/a
12	chr7:65939595-65939645	NHBE	bronchial:	n/a
13	chr7:65939507-65939557	A549	lung:	n/a
14	chr7:65939712-65939762	NHDF-neo	bronchial:	n/a
15	chr7:65939712-65939762	H1-hESC	embryonic stem cell:	embryo
16	chr7:65941812-65941862	HPAEpiC	pulmonary alveolar:	n/a
17	chr7:65939595-65939645	HPAEpiC	pulmonary alveolar:	n/a
18	chr7:65940909-65940959	AG04449	skin:	fetal
19	chr7:65939712-65939762	GM12891	blood:	n/a
20	chr7:65941812-65941862	GM12892	blood:	n/a
21	chr7:65939712-65939762	PFSK-1	brain:	n/a
22	chr7:65941812-65941862	Jurkat	blood:	n/a
23	chr7:65939595-65939645	HCPEpiC	choroid plexus:	n/a
24	chr7:65939507-65939557	GM06990	blood:	n/a
25	chr7:65936514-65936564	HEK293	kidney:	embryo
26	chr7:65938820-65938870	AoSMC	blood vessel:	n/a
27	chr7:65939507-65939557	HPAEpiC	pulmonary alveolar:	n/a
28	chr7:65941812-65941862	H1-hESC	embryonic stem cell:	embryo
29	chr7:65941812-65941862	A549	lung:	n/a
30	chr7:65936514-65936564	ProgFib	skin:	n/a
31	chr7:65940909-65940959	T-47D	breast:	n/a
32	chr7:65939712-65939762	SK-N-SH	brain:	n/a
33	chr7:65940909-65940959	HPAEpiC	pulmonary alveolar:	n/a
34	chr7:65939595-65939645	NB4	blood:	n/a
35	chr7:65939595-65939645	SK-N-MC	brain:	n/a
36	chr7:65938820-65938870	HMEC	breast:	n/a
37	chr7:65941812-65941862	Caco-2	colon:	n/a
38	chr7:65936514-65936564	AG10803	skin:	n/a
39	chr7:65941812-65941862	AG09309	skin:	n/a
40	chr7:65938820-65938870	HRPEpiC	eye:	n/a
41	chr7:65941812-65941862	IMR90	lung:	fetal
42	chr7:65939595-65939645	SAEC	small airway:	n/a
43	chr7:65941812-65941862	PrEC	prostate:	n/a
44	chr7:65939712-65939762	HCM	heart:	n/a
45	chr7:65939507-65939557	GM19239	blood:	n/a
46	chr7:65938820-65938870	SK-N-MC	brain:	n/a
47	chr7:65939595-65939645	Caco-2	colon:	n/a
48	chr7:65936514-65936564	HCM	heart:	n/a
49	chr7:65941812-65941862	GM12878	blood:	n/a
50	chr7:65936514-65936564	HRE	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:65930280..65931785-chr7:66046752..66048531,2	K562	blood:
2	chr7:65540002..65542323-chr7:65893284..65895369,2	K562	blood:
3	chr7:65929041..65931095-chr7:65933234..65935922,2	K562	blood:
4	chr7:65891417..65893045-chr7:65957388..65959846,2	K562	blood:
5	chr7:65579328..65582100-chr7:65915520..65918046,2	K562	blood:
6	chr7:65935517..65938416-chr7:65957047..65958788,2	MCF-7	breast:
7	chr7:65850442..65853165-chr7:65885977..65887755,2	K562	blood:
8	chr7:65886870..65889729-chr7:65890003..65892844,2	K562	blood:
9	chr7:65885885..65889795-chr7:65890003..65893941,4	K562	blood:
10	chr7:65929041..65931095-chr7:65933234..65935922,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TPST1-3	chr7:65908967-65910376	NONHSAT121181
2	lnc-GUSB-14	chr7:65943996-65944083	NONHSAT121184
3	lnc-GUSB-14	chr7:65941250-65941314	NONHSAT147568
4	lnc-GUSB-14	chr7:65943996-65944083	NONHSAT147568
5	lnc-GUSB-11	chr7:65916830-65917175	NONHSAT121180
6	lnc-TPST1-4	chr7:65921737-65922530	NONHSAT121183
7	lnc-GUSB-11	chr7:65908393-65909616	NONHSAT121180
8	lnc-GUSB-14	chr7:65941290-65941314	NONHSAT121184

No data

Variant related genes	Relation type
SKP1P1	TF binding region
ENSG00000230189	TF binding region
ENSG00000267941	TF binding region
ENSG00000252265	TF binding region
ENSG00000236928	TF binding region
SKP1P1	CpG island
ENSG00000230189	CpG island
ENSG00000267941	CpG island
ENSG00000252265	CpG island
ENSG00000236928	CpG island
ENSG00000237310	chromatin interactions
ENSG00000223473	chromatin interactions
ENSG00000126522	chromatin interactions
ENSG00000241258	chromatin interactions
ENSG00000231234	chromatin interactions

Extended variants
information (count: 2360 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:2360 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541868807	chr7:65886461-65886462	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs201784118	chr7:65886528-65886529	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs191606649	chr7:65886531-65886532	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs78591112	chr7:65886533-65886534	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs75327217	chr7:65886534-65886535	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs373374415	chr7:65886535-65886536	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs186636579	chr7:65886562-65886563	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs575357629	chr7:65886569-65886570	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs140131576	chr7:65886583-65886584	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs150292338	chr7:65886676-65886677	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs11291264	chr7:65886750-65886751	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs549725673	chr7:65886751-65886752	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs76804296	chr7:65886752-65886753	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs397889926	chr7:65886767-65886768	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553766946	chr7:65886834-65886835	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs76528019	chr7:65886849-65886850	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs540868929	chr7:65886850-65886851	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs556345265	chr7:65886858-65886859	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs576213139	chr7:65886880-65886881	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs368500909	chr7:65886918-65886919	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs541933970	chr7:65886969-65886970	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs561767275	chr7:65886989-65886990	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs558612588	chr7:65887001-65887002	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs193140050	chr7:65887008-65887009	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs541747242	chr7:65887010-65887011	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs185721233	chr7:65887042-65887043	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs533420448	chr7:65887046-65887047	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs188589631	chr7:65887058-65887059	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs76570778	chr7:65887091-65887092	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs370422155	chr7:65887116-65887117	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs73148663	chr7:65887149-65887150	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs569875415	chr7:65887153-65887154	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs532234579	chr7:65887281-65887282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs549062876	chr7:65887309-65887310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs193176556	chr7:65887321-65887322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs546075352	chr7:65887353-65887354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs377243112	chr7:65887372-65887373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs534722327	chr7:65887450-65887451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561091891	chr7:65887451-65887452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs367568964	chr7:65887488-65887489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs201286251	chr7:65887515-65887516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs184403658	chr7:65887547-65887548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs570656687	chr7:65887561-65887562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs539703093	chr7:65887586-65887587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs78009800	chr7:65887608-65887609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs112087355	chr7:65887652-65887653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs34192067	chr7:65887657-65887658	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs548209413	chr7:65887667-65887668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs117709719	chr7:65887685-65887686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs535574601	chr7:65887694-65887695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
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
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
Follicular lymphoma	20505157	CNVD
Biliary cancer	19435499	CNVD
Williams-beuren syndrome	22470819	CNVD
Acute lymphoblastic leukemia	20067559	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
T-cell prolymphocytic leukemia	17713554	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	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
Glioblastoma	21080181	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
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:754 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:65876200-65888600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr7:65877000-65888600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr7:65879000-65890000	Weak transcription	HSMM	muscle
4	chr7:65879000-65891800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr7:65879000-65893200	Weak transcription	Aorta	Aorta
6	chr7:65879000-65905600	Weak transcription	Lung	lung
7	chr7:65879000-65909000	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr7:65879000-65922200	Weak transcription	Small Intestine	intestine
9	chr7:65879200-65886800	Weak transcription	Brain Hippocampus Middle	brain
10	chr7:65879200-65888600	Weak transcription	Adipose Nuclei	Adipose
11	chr7:65879200-65889600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr7:65879200-65891400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr7:65879200-65893000	Weak transcription	Gastric	stomach
14	chr7:65879200-65893800	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr7:65879200-65894600	Weak transcription	HMEC	breast
16	chr7:65879200-65894800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr7:65879200-65896000	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr7:65879200-65902000	Weak transcription	Brain Substantia Nigra	brain
19	chr7:65879200-65904000	Weak transcription	Fetal Lung	lung
20	chr7:65879200-65907400	Weak transcription	Esophagus	oesophagus
21	chr7:65879200-65924600	Weak transcription	Brain Anterior Caudate	brain
22	chr7:65879200-65939800	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr7:65879200-65946000	Weak transcription	NHEK	skin
24	chr7:65879200-65957600	Weak transcription	Psoas Muscle	Psoas
25	chr7:65879400-65888200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr7:65879400-65889400	Weak transcription	Fetal Muscle Leg	muscle
27	chr7:65879400-65889600	Weak transcription	Primary T cells from cord blood	blood
28	chr7:65879400-65889800	Weak transcription	Ovary	ovary
29	chr7:65879400-65890800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr7:65879400-65891200	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr7:65879400-65891400	Weak transcription	Colonic Mucosa	Colon
32	chr7:65879400-65892600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr7:65879400-65900600	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr7:65879400-65901000	Weak transcription	Brain Angular Gyrus	brain
35	chr7:65879400-65901200	Weak transcription	Stomach Smooth Muscle	stomach
36	chr7:65879400-65909200	Weak transcription	Primary hematopoietic stem cells	blood
37	chr7:65879400-65914200	Weak transcription	Left Ventricle	heart
38	chr7:65879400-65914200	Weak transcription	GM12878-XiMat	blood
39	chr7:65879400-65917200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr7:65879400-65921000	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr7:65879400-65921400	Weak transcription	Fetal Kidney	kidney
42	chr7:65879600-65888600	Weak transcription	Primary T helper cells fromperipheralblood	blood
43	chr7:65879600-65888800	Weak transcription	Fetal Intestine Small	intestine
44	chr7:65879600-65889600	Weak transcription	Fetal Intestine Large	intestine
45	chr7:65879600-65892200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr7:65879600-65893800	Weak transcription	Skeletal Muscle Male	skeletal muscle
47	chr7:65879600-65895000	Weak transcription	Duodenum Mucosa	Duodenum
48	chr7:65879600-65899400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr7:65879600-65900600	Weak transcription	Brain Germinal Matrix	brain
50	chr7:65879600-65907600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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