Variant report

Variant	nsv1043809
Chromosome Location	chr10:54645158-54860817
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1248)
CpG islands
(count:611)
Chromatin interactive
region (count:18)
LncRNA
region (count:27)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1248 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:54766296-54767482	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:54812645-54812845	HepG2	liver:	n/a	n/a
3	ATF2	chr10:54782245-54782835	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr10:54668144-54668733	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr10:54668156-54668650	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr10:54782216-54782718	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr10:54725601-54726237	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr10:54725621-54726197	GM12878	blood:	n/a	n/a
9	ATF2	chr10:54725684-54726190	GM12878	blood:	n/a	n/a
10	ATF2	chr10:54725585-54726269	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr10:54725445-54725479	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr10:54668203-54668557	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr10:54671062-54671223	K562	blood:	n/a	n/a
14	BATF	chr10:54725645-54726140	GM12878	blood:	n/a	n/a
15	BATF	chr10:54725698-54726077	GM12878	blood:	n/a	n/a
16	BATF	chr10:54762789-54763089	GM12878	blood:	n/a	n/a
17	BATF	chr10:54716683-54716935	GM12878	blood:	n/a	n/a
18	BATF	chr10:54724834-54725221	GM12878	blood:	n/a	chr10:54725065-54725076
19	BATF	chr10:54743987-54744184	GM12878	blood:	n/a	chr10:54744116-54744127
20	BATF	chr10:54744003-54744201	GM12878	blood:	n/a	chr10:54744116-54744127
21	BATF	chr10:54716730-54716941	GM12878	blood:	n/a	n/a
22	BATF	chr10:54726691-54727006	GM12878	blood:	n/a	n/a
23	BCL11A	chr10:54683370-54683701	H1-hESC	embryonic stem cell:	n/a	n/a
24	BCL11A	chr10:54725832-54726289	H1-hESC	embryonic stem cell:	n/a	n/a
25	BCL11A	chr10:54782292-54782638	H1-hESC	embryonic stem cell:	n/a	n/a
26	BCL11A	chr10:54725573-54726104	GM12878	blood:	n/a	n/a
27	BCL11A	chr10:54773034-54773276	GM12878	blood:	n/a	n/a
28	BCL11A	chr10:54663343-54663592	H1-hESC	embryonic stem cell:	n/a	n/a
29	BCL11A	chr10:54727856-54728089	H1-hESC	embryonic stem cell:	n/a	n/a
30	BCL11A	chr10:54725683-54726105	GM12878	blood:	n/a	n/a
31	BCL11A	chr10:54828775-54829045	GM12878	blood:	n/a	n/a
32	BCL11A	chr10:54725865-54726110	H1-hESC	embryonic stem cell:	n/a	n/a
33	BCL11A	chr10:54683273-54683616	H1-hESC	embryonic stem cell:	n/a	n/a
34	BCLAF1	chr10:54725338-54726095	GM12878	blood:	n/a	n/a
35	BCLAF1	chr10:54725611-54726184	GM12878	blood:	n/a	n/a
36	BHLHE40	chr10:54828892-54829105	GM12878	blood:	n/a	n/a
37	BHLHE40	chr10:54782709-54782744	GM12878	blood:	n/a	n/a
38	BHLHE40	chr10:54766801-54767080	HepG2	liver:	n/a	n/a
39	BHLHE40	chr10:54727868-54728116	HepG2	liver:	n/a	n/a
40	BHLHE40	chr10:54789662-54789889	GM12878	blood:	n/a	n/a
41	BHLHE40	chr10:54772825-54773371	GM12878	blood:	n/a	n/a
42	BHLHE40	chr10:54765171-54765964	GM12878	blood:	n/a	chr10:54765555-54765568 chr10:54765557-54765566 chr10:54765556-54765565 chr10:54765551-54765572
43	BHLHE40	chr10:54752923-54753221	GM12878	blood:	n/a	n/a
44	BHLHE40	chr10:54744103-54744204	GM12878	blood:	n/a	n/a
45	BHLHE40	chr10:54725319-54726161	GM12878	blood:	n/a	n/a
46	BRCA1	chr10:54725796-54725803	HepG2	liver:	n/a	n/a
47	BRCA1	chr10:54721236-54721259	GM12878	blood:	n/a	n/a
48	CEBPB	chr10:54716151-54716165	HepG2	liver:	n/a	n/a
49	CEBPB	chr10:54725828-54726384	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr10:54736031-54736360	IMR90	lung:	n/a	chr10:54736178-54736189

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:54759379-54759429	U87	brain:	n/a
2	chr10:54759379-54759429	U87	brain:	n/a
3	chr10:54676588-54676638	U87	brain:	n/a
4	chr10:54715153-54715203	Jurkat	blood:	n/a
5	chr10:54782631-54782681	A549	lung:	n/a
6	chr10:54782631-54782681	HEEpiC	esophagus:	n/a
7	chr10:54759379-54759429	BE2_C	brain:	n/a
8	chr10:54676588-54676638	AG09309	skin:	n/a
9	chr10:54714816-54714866	GM12891	blood:	n/a
10	chr10:54714764-54714814	NHBE	bronchial:	n/a
11	chr10:54782631-54782681	HIPEpiC	eye:	n/a
12	chr10:54782631-54782681	HRPEpiC	eye:	n/a
13	chr10:54669084-54669134	HAEpiC	amniotic membrane:	n/a
14	chr10:54715415-54715465	CMK	blood:	n/a
15	chr10:54714816-54714866	H1-hESC	embryonic stem cell:	embryo
16	chr10:54782631-54782681	HNPCEpiC	eye:	n/a
17	chr10:54683341-54683391	HPAEpiC	pulmonary alveolar:	n/a
18	chr10:54782631-54782681	U87	brain:	n/a
19	chr10:54715415-54715465	HAEpiC	amniotic membrane:	n/a
20	chr10:54759379-54759429	AG09319	gingival:	n/a
21	chr10:54676588-54676638	SK-N-MC	brain:	n/a
22	chr10:54759379-54759429	Hela-S3	cervix:	n/a
23	chr10:54676588-54676638	HL-60	blood:	n/a
24	chr10:54669084-54669134	HPAEpiC	pulmonary alveolar:	n/a
25	chr10:54676588-54676638	PrEC	prostate:	n/a
26	chr10:54782631-54782681	LNCaP	prostate:	n/a
27	chr10:54782631-54782681	SK-N-MC	brain:	n/a
28	chr10:54714764-54714814	HAEpiC	amniotic membrane:	n/a
29	chr10:54715153-54715203	LNCaP	prostate:	n/a
30	chr10:54676588-54676638	NHBE	bronchial:	n/a
31	chr10:54715415-54715465	T-47D	breast:	n/a
32	chr10:54715153-54715203	MCF10A-Er-Src	breast:	n/a
33	chr10:54782631-54782681	HCT-116	colon:	n/a
34	chr10:54714764-54714814	GM19239	blood:	n/a
35	chr10:54714764-54714814	GM12878	blood:	n/a
36	chr10:54714816-54714866	GM12892	blood:	n/a
37	chr10:54714816-54714866	RPTEC	kidney:	n/a
38	chr10:54714816-54714866	BJ	skin:	n/a
39	chr10:54715415-54715465	MCF10A-Er-Src	breast:	n/a
40	chr10:54714764-54714814	HCM	heart:	n/a
41	chr10:54715415-54715465	ECC-1	luminal epithelium:	n/a
42	chr10:54714816-54714866	HRE	kidney:	n/a
43	chr10:54715153-54715203	GM06990	blood:	n/a
44	chr10:54714764-54714814	HEEpiC	esophagus:	n/a
45	chr10:54683341-54683391	HNPCEpiC	eye:	n/a
46	chr10:54715153-54715203	HCPEpiC	choroid plexus:	n/a
47	chr10:54714764-54714814	Caco-2	colon:	n/a
48	chr10:54683341-54683391	PANC-1	pancreas:	n/a
49	chr10:54715415-54715465	PANC-1	pancreas:	n/a
50	chr10:54715415-54715465	HCF	heart:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:54764008..54766836-chr10:54772750..54774326,2	K562	blood:
2	chr10:54667605..54669824-chr10:54683197..54686169,2	K562	blood:
3	chr10:54767534..54770532-chr10:54779157..54781249,2	K562	blood:
4	chr10:54711771..54712343-chr7:134236733..134237240,2	MCF-7	breast:
5	chr10:54782310..54784916-chr10:54787401..54789318,3	MCF-7	breast:
6	chr10:54782310..54784916-chr10:54787401..54789318,3	MCF-7	breast:
7	chr10:54752964..54755249-chr10:54757261..54758818,2	K562	blood:
8	chr10:54654118..54656757-chr17:56755700..56758164,2	MCF-7	breast:
9	chr10:54767534..54770532-chr10:54779157..54781249,2	K562	blood:
10	chr10:54769210..54771714-chr10:54777628..54779140,2	K562	blood:
11	chr10:54834743..54836680-chr10:54837690..54840341,2	K562	blood:
12	chr10:54834743..54836680-chr10:54837690..54840341,2	K562	blood:
13	chr10:54769210..54771714-chr10:54777628..54779140,2	K562	blood:
14	chr10:54667605..54669824-chr10:54683197..54686169,2	K562	blood:
15	chr10:54752964..54755249-chr10:54757261..54758818,2	K562	blood:
16	chr10:54793499..54796412-chr10:54801093..54803641,2	MCF-7	breast:
17	chr10:54793499..54796412-chr10:54801093..54803641,2	MCF-7	breast:
18	chr10:54764008..54766836-chr10:54772750..54774326,2	K562	blood:

(count:27 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MBL2-2	chr10:54730759-54733450	XLOC_008826
2	lnc-MBL2-2	chr10:54733248-54733450	XLOC_008826
3	lnc-MBL2-2	chr10:54782584-54782720	NONHSAT013446
4	lnc-MBL2-2	chr10:54735430-54735573	XLOC_008826
5	lnc-MBL2-2	chr10:54782584-54782720	XLOC_008826
6	lnc-DKK1-3	chr10:54798045-54798304	NONHSAT013449
7	lnc-MBL2-2	chr10:54735500-54735573	XLOC_008826
8	lnc-MBL2-8	chr10:54720838-54721360	NONHSAT013440
9	lnc-MBL2-2	chr10:54789671-54789884	XLOC_008826
10	lnc-MBL2-1	chr10:54698381-54698398	XLOC_008825
11	lnc-MBL2-2	chr10:54762812-54762923	NONHSAT013446
12	lnc-MBL2-2	chr10:54782584-54782720	XLOC_008826
13	lnc-MBL2-2	chr10:54789671-54789810	NONHSAT013446
14	lnc-MBL2-2	chr10:54735500-54735573	XLOC_008826
15	lnc-MBL2-2	chr10:54789652-54790030	XLOC_008826
16	lnc-MBL2-1	chr10:54703613-54703837	XLOC_008825
17	lnc-MBL2-2	chr10:54734425-54734560	XLOC_008826
18	lnc-MBL2-2	chr10:54734425-54734597	XLOC_008826
19	lnc-MBL2-2	chr10:54735500-54735575	XLOC_008826
20	lnc-MBL2-2	chr10:54730759-54733450	XLOC_008826
21	lnc-MBL2-2	chr10:54734425-54734560	XLOC_008826
22	lnc-MBL2-8	chr10:54740758-54740831	NONHSAT013440
23	lnc-MBL2-2	chr10:54789671-54789855	XLOC_008826
24	lnc-MBL2-2	chr10:54732073-54733450	XLOC_008826
25	lnc-MBL2-2	chr10:54782584-54782768	XLOC_008826
26	lnc-MBL2-2	chr10:54734425-54734560	XLOC_008826
27	lnc-MBL2-2	chr10:54785024-54785887	XLOC_008826

No data

Variant related genes	Relation type
SNRPEP8	TF binding region
ENSG00000227121	TF binding region
SNRPEP8	CpG island
ENSG00000227121	CpG island
ENSG00000200997	chromatin interactions
GLUD1	miRNA target sites
CNOT10	miRNA target sites
FGFR1	miRNA target sites
PBX2	miRNA target sites
CDC14A	miRNA target sites
MYB	miRNA target sites

Extended variants
information (count: 6855 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:6855 , 50 per page) page: 1 2 3 4 5 6 7 ... 138

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547681438	chr10:54645158-54645159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs372325954	chr10:54645176-54645177	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs566356965	chr10:54645193-54645194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs193186790	chr10:54645199-54645200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs528726984	chr10:54645200-54645201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs540007524	chr10:54645226-54645227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs113238916	chr10:54645241-54645242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs141297975	chr10:54645245-54645246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs570101630	chr10:54645256-54645257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs386743768	chr10:54645322-54645323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs11315400	chr10:54645336-54645337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs535491770	chr10:54645340-54645341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs200235064	chr10:54645345-54645346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs201733441	chr10:54645346-54645347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs113808041	chr10:54645347-54645348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs371103848	chr10:54645348-54645349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs139571124	chr10:54645349-54645350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs145219503	chr10:54645356-54645357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs147013263	chr10:54645382-54645383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs572470181	chr10:54645430-54645431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs545329167	chr10:54645431-54645432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs185417038	chr10:54645436-54645437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs11003246	chr10:54645437-54645438	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs7893804	chr10:54645455-54645456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs577539966	chr10:54645461-54645462	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs148048879	chr10:54645471-54645472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs140882305	chr10:54645531-54645532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs537114646	chr10:54645536-54645537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs190718176	chr10:54645568-54645569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs191094952	chr10:54645597-54645598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs541462606	chr10:54645612-54645613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs183647399	chr10:54645618-54645619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs527280554	chr10:54645619-54645620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs547717977	chr10:54645631-54645632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs188314242	chr10:54645659-54645660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs150099241	chr10:54645671-54645672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs138372593	chr10:54645736-54645737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs376218254	chr10:54645737-54645738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs542759459	chr10:54645770-54645771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs535994271	chr10:54645824-54645825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs76760621	chr10:54645857-54645858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs111714411	chr10:54645889-54645890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs74440636	chr10:54645904-54645905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs371337488	chr10:54645921-54645922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs539805296	chr10:54646000-54646001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs554127777	chr10:54646180-54646181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs113395863	chr10:54646208-54646209	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs545686322	chr10:54646275-54646276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs556275942	chr10:54646276-54646277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs77462563	chr10:54646282-54646283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Obesity	21956041	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Intellectual disability	21948486	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16272173	CNVD
Metanephric adenoma	20802469	CNVD
Autism	20841430	CNVD
Mental retardation	17124404	CNVD
Epilepsy	20923578	CNVD
Prostate cancer	16573809	CNVD
Schizophrenia	19329560	CNVD
Heart failure	18772530	CNVD
Heart failure	18854381	CNVD
Hyperglycemia	19060297	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Glioblastoma multiforme	22286061	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Usher syndrome	20538994	CNVD
Glioblastoma multiforme	17002787	CNVD
Colorectal cancer	16774939	CNVD
Autism	20858243	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:888 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:54641000-54653600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr10:54642600-54647000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr10:54643800-54645200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr10:54644600-54645400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr10:54644600-54647000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr10:54644600-54647200	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr10:54644600-54647200	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr10:54644600-54647200	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr10:54644600-54647200	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr10:54644600-54651600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr10:54645200-54649400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr10:54645400-54645600	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr10:54645600-54646200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr10:54646200-54646400	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr10:54647000-54647600	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr10:54647000-54648000	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr10:54647200-54647400	Enhancers	H9 Cell Line	embryonic stem cell
18	chr10:54647200-54647800	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr10:54647200-54647800	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr10:54647200-54648000	Enhancers	H1 Cell Line	embryonic stem cell
21	chr10:54647200-54648000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr10:54647200-54648000	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr10:54647800-54651600	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr10:54647800-54652000	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr10:54648000-54651600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr10:54648000-54653200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr10:54649000-54649400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr10:54649400-54650400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr10:54649400-54650400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr10:54650200-54650400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr10:54650200-54650400	Bivalent Enhancer	Fetal Stomach	stomach
32	chr10:54650400-54653600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr10:54651000-54654000	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr10:54651600-54652000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr10:54651600-54652200	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr10:54651600-54652200	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr10:54651600-54652400	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr10:54651800-54652200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr10:54652000-54652400	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr10:54652200-54655800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr10:54653200-54654200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr10:54653400-54654200	Enhancers	Fetal Intestine Large	intestine
43	chr10:54653400-54654400	Enhancers	Fetal Intestine Small	intestine
44	chr10:54653600-54653800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr10:54653600-54654400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr10:54653600-54657400	Enhancers	HMEC	breast
47	chr10:54653600-54657600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr10:54653800-54654000	Enhancers	NHEK	skin
49	chr10:54654000-54654400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr10:54654400-54657600	Enhancers	Breast Myoepithelial Primary Cells	Breast

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