Variant report

Variant	nsv603007
Chromosome Location	chr6:44909515-45008779
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:44928633-44929024	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:44918920-44919276	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:44942228-44942585	K562	blood:	n/a	n/a
4	ARID3A	chr6:44934203-44935340	K562	blood:	n/a	n/a
5	ATF1	chr6:44934477-44934865	K562	blood:	n/a	n/a
6	ATF2	chr6:44966735-44967151	GM12878	blood:	n/a	n/a
7	ATF2	chr6:44966734-44967257	GM12878	blood:	n/a	n/a
8	ATF3	chr6:44934407-44934925	K562	blood:	n/a	n/a
9	BACH1	chr6:44965357-44965412	K562	blood:	n/a	n/a
10	BATF	chr6:44977334-44977648	GM12878	blood:	n/a	chr6:44977540-44977551
11	BATF	chr6:44947204-44947474	GM12878	blood:	n/a	n/a
12	BATF	chr6:44966783-44967196	GM12878	blood:	n/a	n/a
13	BATF	chr6:44966841-44967148	GM12878	blood:	n/a	n/a
14	BATF	chr6:44977286-44977716	GM12878	blood:	n/a	chr6:44977540-44977551
15	BCL3	chr6:44934546-44934913	K562	blood:	n/a	n/a
16	BHLHE40	chr6:44928669-44928955	GM12878	blood:	n/a	n/a
17	BHLHE40	chr6:44934500-44934832	K562	blood:	n/a	n/a
18	BHLHE40	chr6:44969459-44969727	GM12878	blood:	n/a	n/a
19	CBX3	chr6:44934407-44934915	K562	blood:	n/a	n/a
20	CBX3	chr6:44940439-44940814	K562	blood:	n/a	n/a
21	CBX3	chr6:44934427-44934905	HCT-116	colon:	n/a	n/a
22	CBX3	chr6:44928552-44929041	HCT-116	colon:	n/a	n/a
23	CBX3	chr6:44934371-44934913	HCT-116	colon:	n/a	n/a
24	CBX3	chr6:44934470-44934850	K562	blood:	n/a	n/a
25	CBX3	chr6:44940388-44940854	K562	blood:	n/a	n/a
26	CCNT2	chr6:45003117-45003383	K562	blood:	n/a	n/a
27	CCNT2	chr6:44934499-44934885	K562	blood:	n/a	n/a
28	CEBPB	chr6:44963658-44963730	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr6:44946246-44946503	HepG2	liver:	n/a	n/a
30	CEBPB	chr6:45000205-45000525	Hela-S3	cervix:	n/a	chr6:45000351-45000360 chr6:45000350-45000361 chr6:45000351-45000360 chr6:45000351-45000360 chr6:45000349-45000362
31	CEBPB	chr6:45000180-45000537	K562	blood:	n/a	chr6:45000351-45000360 chr6:45000350-45000361 chr6:45000351-45000360 chr6:45000351-45000360 chr6:45000349-45000362
32	CEBPB	chr6:45000179-45000543	IMR90	lung:	n/a	chr6:45000351-45000360 chr6:45000350-45000361 chr6:45000351-45000360 chr6:45000351-45000360 chr6:45000349-45000362
33	CEBPB	chr6:44934462-44934822	IMR90	lung:	n/a	chr6:44934624-44934633
34	CEBPB	chr6:44934384-44934901	K562	blood:	n/a	chr6:44934624-44934633
35	CEBPB	chr6:44993903-44994225	K562	blood:	n/a	chr6:44994071-44994082 chr6:44994071-44994080 chr6:44994069-44994082 chr6:44994069-44994080 chr6:44994069-44994082
36	CEBPB	chr6:45000170-45000547	HepG2	liver:	n/a	chr6:45000351-45000360 chr6:45000350-45000361 chr6:45000351-45000360 chr6:45000351-45000360 chr6:45000349-45000362
37	CEBPB	chr6:44934437-44934855	Hela-S3	cervix:	n/a	chr6:44934624-44934633
38	CEBPB	chr6:44963269-44963657	K562	blood:	n/a	n/a
39	CEBPB	chr6:45000190-45000522	A549	lung:	n/a	chr6:45000351-45000360 chr6:45000350-45000361 chr6:45000351-45000360 chr6:45000351-45000360 chr6:45000349-45000362
40	CEBPB	chr6:45000214-45000566	ECC-1	luminal epithelium:	n/a	chr6:45000351-45000360 chr6:45000350-45000361 chr6:45000351-45000360 chr6:45000351-45000360 chr6:45000349-45000362
41	CEBPB	chr6:44982107-44982316	HepG2	liver:	n/a	n/a
42	CEBPB	chr6:44944620-44944869	HepG2	liver:	n/a	chr6:44944700-44944711
43	CEBPB	chr6:44934324-44934972	HCT-116	colon:	n/a	chr6:44934911-44934923 chr6:44934624-44934633
44	CEBPB	chr6:44937623-44937821	IMR90	lung:	n/a	n/a
45	CEBPB	chr6:44993799-44994231	MCF-7	breast:	n/a	chr6:44994071-44994082 chr6:44994071-44994080 chr6:44994069-44994082 chr6:44994069-44994080 chr6:44994069-44994082
46	CEBPB	chr6:45000177-45000491	ECC-1	luminal epithelium:	n/a	chr6:45000351-45000360 chr6:45000350-45000361 chr6:45000351-45000360 chr6:45000351-45000360 chr6:45000349-45000362
47	CEBPB	chr6:44993905-44994180	MCF-7	breast:	n/a	chr6:44994071-44994082 chr6:44994071-44994080 chr6:44994069-44994082 chr6:44994069-44994080 chr6:44994069-44994082
48	CEBPB	chr6:45000229-45000574	MCF-7	breast:	n/a	chr6:45000351-45000360 chr6:45000350-45000361 chr6:45000351-45000360 chr6:45000351-45000360 chr6:45000349-45000362
49	CEBPB	chr6:44934173-44934989	K562	blood:	n/a	chr6:44934911-44934923 chr6:44934624-44934633
50	CEBPB	chr6:44993872-44994249	Hela-S3	cervix:	n/a	chr6:44994071-44994082 chr6:44994071-44994080 chr6:44994069-44994082 chr6:44994069-44994080 chr6:44994069-44994082

No.	Distal block	Cell Line	Cell type
1	chr6:44974489..44977160-chr6:44980461..44983338,2	K562	blood:
2	chr6:44917876..44920561-chr6:44920562..44922585,2	MCF-7	breast:
3	chr6:44963271..44965402-chr6:44968999..44972162,3	K562	blood:
4	chr6:44962823..44965402-chr6:44970662..44972612,2	K562	blood:
5	chr6:44987589..44991130-chr6:44992558..44996333,3	K562	blood:
6	chr6:44917876..44920561-chr6:44920562..44922585,2	MCF-7	breast:
7	chr6:45003285..45005012-chr6:45007518..45010080,2	K562	blood:
8	chr6:44972423..44974259-chr6:44978944..44980911,2	K562	blood:
9	chr6:44987108..44989743-chr6:44993654..44995647,2	K562	blood:
10	chr6:44987589..44991130-chr6:44992558..44996333,3	K562	blood:
11	chr6:45003285..45005012-chr6:45007518..45010080,2	K562	blood:
12	chr6:44996729..44999425-chr6:45119837..45121459,2	K562	blood:
13	chr6:44917939..44922059-chr6:44925666..44928514,3	K562	blood:
14	chr6:44935484..44938452-chr6:44939240..44940813,2	K562	blood:
15	chr6:44917939..44922059-chr6:44925666..44928514,3	K562	blood:
16	chr6:44924333..44926933-chr6:44928218..44930920,2	K562	blood:
17	chr6:44987108..44989743-chr6:44993654..44995647,2	K562	blood:
18	chr6:44963271..44965402-chr6:44968999..44972162,3	K562	blood:
19	chr6:44949240..44952197-chr6:44957383..44960219,3	K562	blood:
20	chr6:44928658..44930221-chr6:45326668..45328264,2	K562	blood:
21	chr6:44974489..44977160-chr6:44980461..44983338,2	K562	blood:
22	chr6:44924333..44926933-chr6:44928218..44930920,2	K562	blood:
23	chr6:44935484..44938452-chr6:44939240..44940813,2	K562	blood:
24	chr6:44962823..44965402-chr6:44970662..44972612,2	K562	blood:
25	chr6:44949240..44952197-chr6:44957383..44960219,3	K562	blood:
26	chr6:44972423..44974259-chr6:44978944..44980911,2	K562	blood:

Variant related genes	Relation type
SUPT3H	TF binding region

Extended variants
information (count: 3637 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:3637 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1329715	chr6:44909515-44909516	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs62436393	chr6:44909517-44909518	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs75006888	chr6:44909518-44909519	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs561341053	chr6:44909532-44909533	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs145520653	chr6:44909572-44909573	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs183441501	chr6:44909683-44909684	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs1402597	chr6:44909730-44909731	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs533000650	chr6:44909736-44909737	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs551513782	chr6:44909765-44909766	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs115678023	chr6:44909797-44909798	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs530168340	chr6:44909799-44909800	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs73735264	chr6:44909803-44909804	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs371829981	chr6:44909820-44909821	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs144029670	chr6:44909825-44909826	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs567651890	chr6:44909826-44909827	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs192549375	chr6:44909827-44909828	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs146438087	chr6:44909871-44909872	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs571861976	chr6:44909885-44909886	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs550137880	chr6:44909892-44909893	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs140759499	chr6:44909965-44909966	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs576099949	chr6:44909977-44909978	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs143395964	chr6:44909999-44910000	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs570110199	chr6:44910031-44910032	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs563893433	chr6:44910032-44910033	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs201488466	chr6:44910033-44910034	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs74497282	chr6:44910043-44910044	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs575332995	chr6:44910044-44910045	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs573317213	chr6:44910073-44910074	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs184348673	chr6:44910195-44910196	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs540595422	chr6:44910213-44910214	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs376475587	chr6:44910220-44910221	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs188140298	chr6:44910238-44910239	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs577861104	chr6:44910247-44910248	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs544921890	chr6:44910254-44910255	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs561465313	chr6:44910271-44910272	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs563476203	chr6:44910312-44910313	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs192741123	chr6:44910313-44910314	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs576696622	chr6:44910458-44910459	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs549517075	chr6:44910468-44910469	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs558041740	chr6:44910479-44910480	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs184484732	chr6:44910508-44910509	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs528499597	chr6:44910547-44910548	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs546930486	chr6:44910549-44910550	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs656463	chr6:44910589-44910590	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs539314228	chr6:44910645-44910646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs550918385	chr6:44910721-44910722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs115297634	chr6:44910723-44910724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs536413477	chr6:44910733-44910734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs573621579	chr6:44910737-44910738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs189188970	chr6:44910744-44910745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Osteosarcoma	16790693	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Osteosarcoma	21197465	CNVD
Gastric cancer	24379144	CNVD
Neuroblastoma	18923191	CNVD
abnormal development	18461090	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16790693	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Systemic lupus erythematosus	19287148	CNVD
Colorectal cancer	19359472	CNVD
Multiple myeloma	16616336	CNVD
Chordoma	18071362	CNVD
Follicular lymphoma	16790693	CNVD
Osteosarcoma	19286668	CNVD
Neurocytoma	17123091	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Ovarian cancer	20844748	CNVD
lymphocytic leukemia	21291569	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:528 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:44895800-44910200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr6:44904400-44918800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
3	chr6:44905200-44913200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr6:44906800-44913400	Weak transcription	HSMM	muscle
5	chr6:44908000-44910400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr6:44908600-44910000	ZNF genes & repeats	Dnd41	blood
7	chr6:44909200-44909800	Weak transcription	Primary hematopoietic stem cells	blood
8	chr6:44909200-44914200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr6:44910000-44910200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr6:44910000-44913400	Weak transcription	Dnd41	blood
11	chr6:44910200-44910600	ZNF genes & repeats	Aorta	Aorta
12	chr6:44910600-44913600	Weak transcription	Aorta	Aorta
13	chr6:44912400-44913200	Weak transcription	Primary T cells from cord blood	blood
14	chr6:44912600-44913400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr6:44913000-44914600	Weak transcription	Ovary	ovary
16	chr6:44913200-44913600	ZNF genes & repeats	Primary T cells from cord blood	blood
17	chr6:44913200-44913800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
18	chr6:44913200-44913800	ZNF genes & repeats	Primary B cells from cord blood	blood
19	chr6:44913200-44914600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr6:44913200-44914600	ZNF genes & repeats	Fetal Heart	heart
21	chr6:44913200-44914800	ZNF genes & repeats	Primary hematopoietic stem cells	blood
22	chr6:44913200-44914800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr6:44913400-44914000	ZNF genes & repeats	Adipose Nuclei	Adipose
24	chr6:44913400-44914000	ZNF genes & repeats	HSMM	muscle
25	chr6:44913400-44914600	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr6:44913400-44915000	ZNF genes & repeats	Dnd41	blood
27	chr6:44913400-44930000	Weak transcription	Pancreas	Pancrea
28	chr6:44913600-44928600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr6:44913800-44918200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr6:44914000-44914800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
31	chr6:44914000-44922800	Weak transcription	HSMM	muscle
32	chr6:44914200-44914400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr6:44914200-44914600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
34	chr6:44914200-44914800	ZNF genes & repeats	Aorta	Aorta
35	chr6:44914400-44915000	Weak transcription	Colon Smooth Muscle	Colon
36	chr6:44914400-44919200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr6:44914600-44914800	ZNF genes & repeats	Ovary	ovary
38	chr6:44914600-44915200	Strong transcription	Fetal Heart	heart
39	chr6:44914600-44917200	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr6:44914600-44923000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr6:44914800-44917000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr6:44914800-44919200	Weak transcription	Aorta	Aorta
43	chr6:44915000-44917200	Weak transcription	Dnd41	blood
44	chr6:44915200-44917400	Weak transcription	Fetal Heart	heart
45	chr6:44915400-44932800	Weak transcription	Left Ventricle	heart
46	chr6:44916000-44923600	Weak transcription	Stomach Smooth Muscle	stomach
47	chr6:44916600-44922600	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr6:44916800-44917400	Weak transcription	Colon Smooth Muscle	Colon
49	chr6:44917000-44919600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
50	chr6:44917200-44917800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell

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