Variant report

Variant	esv1815526
Chromosome Location	chr7:65286678-65338375
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:561)
CpG islands
(count:427)
Chromatin interactive
region (count:12)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:561 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:65301736-65302051	K562	blood:	n/a	n/a
2	ARID3A	chr7:65301784-65302028	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:65317529-65317586	HepG2	liver:	n/a	n/a
4	ATF1	chr7:65302462-65302647	K562	blood:	n/a	n/a
5	BACH1	chr7:65338017-65338205	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr7:65302528-65302815	K562	blood:	n/a	n/a
7	BRCA1	chr7:65305283-65305337	GM12878	blood:	n/a	n/a
8	CBX3	chr7:65313184-65313538	K562	blood:	n/a	n/a
9	CBX3	chr7:65305453-65305819	K562	blood:	n/a	n/a
10	CBX3	chr7:65302488-65302854	K562	blood:	n/a	n/a
11	CCNT2	chr7:65300352-65300552	K562	blood:	n/a	n/a
12	CCNT2	chr7:65337783-65338592	K562	blood:	n/a	chr7:65338186-65338195
13	CEBPB	chr7:65316853-65317020	Hela-S3	cervix:	n/a	chr7:65316972-65316983
14	CEBPB	chr7:65317549-65317757	A549	lung:	n/a	n/a
15	CEBPB	chr7:65313890-65313913	HepG2	liver:	n/a	chr7:65313890-65313901
16	CEBPB	chr7:65316843-65317061	K562	blood:	n/a	chr7:65316972-65316983
17	CEBPB	chr7:65316813-65317139	K562	blood:	n/a	chr7:65316972-65316983
18	CEBPB	chr7:65316917-65317009	HepG2	liver:	n/a	chr7:65316972-65316983
19	CEBPB	chr7:65316797-65317059	K562	blood:	n/a	chr7:65316972-65316983
20	CEBPB	chr7:65332776-65332976	HepG2	liver:	n/a	chr7:65332889-65332900
21	CEBPB	chr7:65308651-65308852	HepG2	liver:	n/a	chr7:65308694-65308705 chr7:65308693-65308706
22	CEBPB	chr7:65337762-65338153	IMR90	lung:	n/a	n/a
23	CEBPB	chr7:65317457-65317641	HepG2	liver:	n/a	n/a
24	CEBPB	chr7:65334430-65334653	IMR90	lung:	n/a	n/a
25	CEBPB	chr7:65313883-65313907	IMR90	lung:	n/a	chr7:65313890-65313901
26	CEBPB	chr7:65302565-65302719	K562	blood:	n/a	n/a
27	CEBPB	chr7:65332878-65332911	K562	blood:	n/a	chr7:65332889-65332900
28	CEBPB	chr7:65319992-65320101	HepG2	liver:	n/a	chr7:65320028-65320039
29	CEBPB	chr7:65319952-65320112	K562	blood:	n/a	chr7:65320028-65320039
30	CEBPB	chr7:65332768-65333066	IMR90	lung:	n/a	chr7:65332889-65332900
31	CEBPB	chr7:65289893-65289961	A549	lung:	n/a	n/a
32	CEBPB	chr7:65302559-65302726	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr7:65337697-65338239	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr7:65302461-65302809	IMR90	lung:	n/a	n/a
35	CEBPB	chr7:65289910-65289963	K562	blood:	n/a	n/a
36	CEBPB	chr7:65302541-65302720	K562	blood:	n/a	n/a
37	CEBPB	chr7:65338072-65338234	HepG2	liver:	n/a	n/a
38	CEBPB	chr7:65337913-65338272	HepG2	liver:	n/a	n/a
39	CEBPB	chr7:65338009-65338209	K562	blood:	n/a	n/a
40	CEBPB	chr7:65332341-65332420	K562	blood:	n/a	chr7:65332396-65332407
41	CEBPB	chr7:65305553-65305716	K562	blood:	n/a	n/a
42	CEBPB	chr7:65334430-65334631	A549	lung:	n/a	n/a
43	CEBPB	chr7:65338012-65338138	A549	lung:	n/a	n/a
44	CEBPB	chr7:65302514-65302800	A549	lung:	n/a	n/a
45	CEBPB	chr7:65332307-65332445	HepG2	liver:	n/a	chr7:65332396-65332407
46	CEBPD	chr7:65337963-65338299	HepG2	liver:	n/a	n/a
47	CHD2	chr7:65337705-65338547	Hela-S3	cervix:	n/a	n/a
48	CREB1	chr7:65337861-65338372	K562	blood:	n/a	n/a
49	CREB1	chr7:65337827-65338529	HepG2	liver:	n/a	n/a
50	CREB1	chr7:65337864-65338263	A549	lung:	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	chr7:65338055-65338105	RPTEC	kidney:	n/a
2	chr7:65338055-65338105	HEEpiC	esophagus:	n/a
3	chr7:65302258-65302308	HCM	heart:	n/a
4	chr7:65302258-65302308	NT2-D1	testis:	n/a
5	chr7:65334477-65334527	PFSK-1	brain:	n/a
6	chr7:65337924-65337974	IMR90	lung:	fetal
7	chr7:65334477-65334527	LNCaP	prostate:	n/a
8	chr7:65303149-65303199	HPAEpiC	pulmonary alveolar:	n/a
9	chr7:65303149-65303199	H1-hESC	embryonic stem cell:	embryo
10	chr7:65303149-65303199	CMK	blood:	n/a
11	chr7:65337924-65337974	H1-hESC	embryonic stem cell:	embryo
12	chr7:65337924-65337974	HRE	kidney:	n/a
13	chr7:65315216-65315266	SKMC	muscle:	n/a
14	chr7:65337924-65337974	AoSMC	blood vessel:	n/a
15	chr7:65338055-65338105	SK-N-MC	brain:	n/a
16	chr7:65338055-65338105	NB4	blood:	n/a
17	chr7:65337895-65337945	HCM	heart:	n/a
18	chr7:65303149-65303199	AG09319	gingival:	n/a
19	chr7:65302258-65302308	HEK293	kidney:	embryo
20	chr7:65338055-65338105	NHBE	bronchial:	n/a
21	chr7:65334477-65334527	HIPEpiC	eye:	n/a
22	chr7:65315216-65315266	PANC-1	pancreas:	n/a
23	chr7:65337924-65337974	NT2-D1	testis:	n/a
24	chr7:65302258-65302308	NH-A	brain:	n/a
25	chr7:65303149-65303199	HCF	heart:	n/a
26	chr7:65338055-65338105	HRCEpiC	kidney:	n/a
27	chr7:65337924-65337974	HPAEpiC	pulmonary alveolar:	n/a
28	chr7:65337924-65337974	GM06990	blood:	n/a
29	chr7:65338055-65338105	AG09309	skin:	n/a
30	chr7:65337895-65337945	ECC-1	luminal epithelium:	n/a
31	chr7:65315216-65315266	A549	lung:	n/a
32	chr7:65337924-65337974	HEK293	kidney:	embryo
33	chr7:65334477-65334527	H1-hESC	embryonic stem cell:	embryo
34	chr7:65337924-65337974	HMEC	breast:	n/a
35	chr7:65337895-65337945	SK-N-MC	brain:	n/a
36	chr7:65334477-65334527	U87	brain:	n/a
37	chr7:65337924-65337974	T-47D	breast:	n/a
38	chr7:65302258-65302308	HCF	heart:	n/a
39	chr7:65338055-65338105	BE2_C	brain:	n/a
40	chr7:65315216-65315266	HNPCEpiC	eye:	n/a
41	chr7:65338055-65338105	AoSMC	blood vessel:	n/a
42	chr7:65334477-65334527	PANC-1	pancreas:	n/a
43	chr7:65302258-65302308	NHDF-neo	bronchial:	n/a
44	chr7:65338055-65338105	SKMC	muscle:	n/a
45	chr7:65315216-65315266	HUVEC	blood vessel:	n/a
46	chr7:65337895-65337945	BJ	skin:	n/a
47	chr7:65337895-65337945	SK-N-SH	brain:	n/a
48	chr7:65303149-65303199	HEEpiC	esophagus:	n/a
49	chr7:65302258-65302308	SAEC	small airway:	n/a
50	chr7:65337895-65337945	GM12892	blood:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:65303936..65305643-chr7:65310020..65312064,2	MCF-7	breast:
2	chr7:64498559..64499288-chr7:65338067..65339051,2	NB4	blood:
3	chr7:65287691..65289965-chr7:65292443..65295054,2	K562	blood:
4	chr7:65337864..65339398-chr7:65445758..65448693,2	K562	blood:
5	chr11:62609016..62609720-chr7:65338341..65338852,2	Hela-S3	cervix:
6	chr7:65296135..65298930-chr7:65301259..65302803,2	K562	blood:
7	chr7:65290518..65293145-chr7:65296020..65298724,2	MCF-7	breast:
8	chr7:65287691..65289965-chr7:65292443..65295054,2	K562	blood:
9	chr7:65214366..65217502-chr7:65337041..65339664,3	MCF-7	breast:
10	chr7:64498619..64500351-chr7:65337220..65338727,3	MCF-7	breast:
11	chr7:65296135..65298930-chr7:65301259..65302803,2	K562	blood:
12	chr7:65290518..65293145-chr7:65296020..65298724,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-VKORC1L1-4	chr7:65318013-65318060	NONHSAT121122
2	lnc-VKORC1L1-1	chr7:65292534-65292729	XLOC_006132
3	lnc-VKORC1L1-1	chr7:65293604-65293652	XLOC_006132
4	lnc-VKORC1L1-4	chr7:65300762-65300945	NONHSAT121122
5	lnc-VKORC1L1-4	chr7:65303020-65303077	NONHSAT121122
6	lnc-VKORC1L1-2	chr7:65286972-65287116	ENSG00000249705
7	lnc-VKORC1L1-3	chr7:65305199-65305583	NONHSAT121123

No data

Variant related genes	Relation type
ENSG00000236529	TF binding region
RNU6-973P	TF binding region
VKORC1L1	TF binding region
ENSG00000236529	CpG island
RNU6-973P	CpG island
VKORC1L1	CpG island
ENSG00000236529	chromatin interactions
ENSG00000239985	chromatin interactions
ENSG00000234585	chromatin interactions
ENSG00000169919	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000228409	chromatin interactions
FOXP1	miRNA target sites

Extended variants
information (count: 1581 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:1581 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12537026	chr7:65286697-65286698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs386714053	chr7:65286711-65286712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs4452696	chr7:65286712-65286713	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs538840694	chr7:65286715-65286716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs112730199	chr7:65286722-65286723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs373328955	chr7:65286724-65286725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs371690899	chr7:65286727-65286728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs12540309	chr7:65286761-65286762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs139046367	chr7:65286806-65286807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs59847374	chr7:65286807-65286808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs397965222	chr7:65286809-65286810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs60571067	chr7:65286815-65286816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs569370797	chr7:65286816-65286817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs538383222	chr7:65286874-65286875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs139857199	chr7:65286885-65286886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs61577036	chr7:65286887-65286888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs554959251	chr7:65286922-65286923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs373570550	chr7:65286927-65286928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs113364063	chr7:65286930-65286931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs148923758	chr7:65286931-65286932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs58512437	chr7:65286932-65286933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs59543325	chr7:65286947-65286948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554120187	chr7:65286949-65286950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs574742444	chr7:65286965-65286966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs112990537	chr7:65286966-65286967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs553007000	chr7:65286967-65286968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs372962726	chr7:65286986-65286987	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs190929928	chr7:65287021-65287022	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs564788153	chr7:65287022-65287023	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs183078613	chr7:65287045-65287046	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs543914921	chr7:65287065-65287066	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs35009664	chr7:65287069-65287070	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs529680992	chr7:65287083-65287084	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs547239557	chr7:65287099-65287100	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs542770127	chr7:65287100-65287101	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs13242173	chr7:65287122-65287123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs113779286	chr7:65287145-65287146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs111403331	chr7:65287154-65287155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs36020095	chr7:65287221-65287222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs367833464	chr7:65287239-65287240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs377572611	chr7:65287244-65287245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs58603109	chr7:65287245-65287246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs143931894	chr7:65287255-65287256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs58234605	chr7:65287257-65287258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs569482033	chr7:65287324-65287325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs538295421	chr7:65287332-65287333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs547755733	chr7:65287334-65287335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs543891198	chr7:65287340-65287341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs35651853	chr7:65287376-65287377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs548414764	chr7:65287378-65287379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:313 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:65247800-65303400	Weak transcription	Duodenum Mucosa	Duodenum
2	chr7:65260800-65302600	Weak transcription	Gastric	stomach
3	chr7:65264000-65302600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr7:65264000-65302800	Weak transcription	Esophagus	oesophagus
5	chr7:65264000-65310800	Weak transcription	Fetal Intestine Small	intestine
6	chr7:65264200-65292400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr7:65264600-65292800	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr7:65265600-65304400	Weak transcription	Left Ventricle	heart
9	chr7:65266800-65311000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr7:65267600-65304000	Weak transcription	Placenta	Placenta
11	chr7:65270200-65302800	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr7:65273400-65305400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr7:65273800-65303200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr7:65274600-65303000	Weak transcription	Stomach Smooth Muscle	stomach
15	chr7:65275200-65290800	Weak transcription	Pancreas	Pancrea
16	chr7:65275200-65304000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr7:65285600-65294200	Weak transcription	Spleen	Spleen
18	chr7:65288200-65292200	Weak transcription	Rectal Mucosa Donor 29	rectum
19	chr7:65288800-65306000	Weak transcription	Aorta	Aorta
20	chr7:65290400-65290600	Enhancers	HepG2	liver
21	chr7:65290400-65305800	Weak transcription	GM12878-XiMat	blood
22	chr7:65290600-65294600	Weak transcription	HepG2	liver
23	chr7:65290800-65292000	Strong transcription	Pancreas	Pancrea
24	chr7:65291000-65295600	Weak transcription	Adipose Nuclei	Adipose
25	chr7:65291200-65302200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr7:65292000-65292400	Weak transcription	Pancreas	Pancrea
27	chr7:65292200-65292800	Strong transcription	Rectal Mucosa Donor 29	rectum
28	chr7:65292400-65292800	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr7:65292400-65292800	Strong transcription	Pancreas	Pancrea
30	chr7:65292400-65293000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr7:65292800-65301200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr7:65292800-65302600	Weak transcription	Pancreas	Pancrea
33	chr7:65292800-65303800	Weak transcription	Rectal Mucosa Donor 29	rectum
34	chr7:65294200-65298400	Weak transcription	Psoas Muscle	Psoas
35	chr7:65297200-65305000	Weak transcription	Small Intestine	intestine
36	chr7:65297400-65311000	Weak transcription	Liver	Liver
37	chr7:65300200-65300400	Enhancers	K562	blood
38	chr7:65300200-65300600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
39	chr7:65300200-65300600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr7:65300400-65302600	Weak transcription	K562	blood
41	chr7:65301200-65301400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr7:65301200-65303000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr7:65301200-65303000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr7:65301200-65303800	Weak transcription	Duodenum Smooth Muscle	Duodenum
45	chr7:65301400-65302600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr7:65302200-65311000	Weak transcription	Right Ventricle	heart
47	chr7:65302400-65302800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr7:65302400-65302800	Enhancers	HUVEC	blood vessel
49	chr7:65302400-65302800	Enhancers	NHEK	skin
50	chr7:65302400-65303000	Enhancers	Hela-S3	cervix

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