Variant report

Variant	nsv895564
Chromosome Location	chr10:61220923-61327502
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:508)
CpG islands
(count:122)
Chromatin interactive
region (count:8)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:508 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr10:61230437-61230594	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL3	chr10:61252968-61253263	GM12878	blood:	n/a	n/a
3	CEBPB	chr10:61284607-61284826	HepG2	liver:	n/a	n/a
4	CEBPB	chr10:61248548-61248824	HepG2	liver:	n/a	n/a
5	CEBPB	chr10:61265502-61265793	HepG2	liver:	n/a	chr10:61265626-61265637
6	CEBPB	chr10:61223748-61224325	HepG2	liver:	n/a	chr10:61224185-61224198 chr10:61224185-61224196 chr10:61224186-61224197
7	CEBPB	chr10:61278773-61279075	A549	lung:	n/a	n/a
8	CEBPB	chr10:61224057-61224328	IMR90	lung:	n/a	chr10:61224185-61224198 chr10:61224185-61224196 chr10:61224186-61224197
9	CEBPB	chr10:61284556-61284777	A549	lung:	n/a	n/a
10	CEBPB	chr10:61284515-61284817	IMR90	lung:	n/a	n/a
11	CEBPB	chr10:61265581-61265774	K562	blood:	n/a	chr10:61265626-61265637
12	CEBPB	chr10:61313403-61313433	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr10:61248576-61248776	A549	lung:	n/a	n/a
14	CEBPB	chr10:61265497-61265772	IMR90	lung:	n/a	chr10:61265626-61265637
15	CTCF	chr10:61224920-61225070	HRPEpiC	eye:	n/a	n/a
16	CTCF	chr10:61224940-61225090	HMEC	breast:	n/a	n/a
17	CTCF	chr10:61296440-61296590	AG04450	lung:	n/a	n/a
18	CTCF	chr10:61224900-61225050	HA-sp	spinal cord:	n/a	n/a
19	CTCF	chr10:61225019-61225039	Hela-S3	cervix:	n/a	n/a
20	CTCF	chr10:61224940-61225090	BE2_C	brain:	n/a	n/a
21	CTCF	chr10:61224908-61225114	MCF-7	breast:	n/a	n/a
22	CTCF	chr10:61224964-61225062	GM12878	blood:	n/a	n/a
23	CTCF	chr10:61313200-61313350	HBMEC	blood vessel:	n/a	n/a
24	CTCF	chr10:61313160-61313310	SK-N-SH_RA	brain:	n/a	n/a
25	CTCF	chr10:61224960-61225110	NHDF-neo	bronchial:	n/a	n/a
26	CTCF	chr10:61224747-61225246	HCT-116	colon:	n/a	n/a
27	CTCF	chr10:61230774-61230865	GM19238	blood:	n/a	n/a
28	CTCF	chr10:61273320-61273470	SK-N-SH_RA	brain:	n/a	n/a
29	CTCF	chr10:61224940-61225090	HCFaa	heart:	n/a	n/a
30	CTCF	chr10:61224797-61225165	MCF-7	breast:	n/a	n/a
31	CTCF	chr10:61224920-61225070	SAEC	small airway:	n/a	n/a
32	CTCF	chr10:61224925-61225088	ProgFib	skin:	n/a	n/a
33	CTCF	chr10:61224920-61225070	AG09319	gingival:	n/a	n/a
34	CTCF	chr10:61252964-61253062	MCF-7	breast:	n/a	n/a
35	CTCF	chr10:61224940-61225090	HBMEC	blood vessel:	n/a	n/a
36	CTCF	chr10:61252984-61253044	MCF-7	breast:	n/a	n/a
37	CTCF	chr10:61224960-61225110	MCF-7	breast:	n/a	n/a
38	CTCF	chr10:61267320-61267470	HMF	breast:	n/a	n/a
39	CTCF	chr10:61224920-61225070	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr10:61224880-61225030	BE2_C	brain:	n/a	n/a
41	CTCF	chr10:61267260-61267410	NHDF-neo	bronchial:	n/a	n/a
42	CTCF	chr10:61267240-61267390	HCM	heart:	n/a	n/a
43	CTCF	chr10:61224920-61225070	MCF-7	breast:	n/a	n/a
44	CTCF	chr10:61224940-61225090	AG09309	skin:	n/a	n/a
45	CTCF	chr10:61224880-61225030	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr10:61313240-61313390	A549	lung:	n/a	n/a
47	CTCF	chr10:61224940-61225090	AG09319	gingival:	n/a	n/a
48	CTCF	chr10:61302555-61302627	LNCaP	prostate:	n/a	n/a
49	CTCF	chr10:61224773-61225204	HepG2	liver:	n/a	n/a
50	CTCF	chr10:61256179-61256230	GM10248	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:61297420-61297470	NHDF-neo	bronchial:	n/a
2	chr10:61320994-61321044	HPAEpiC	pulmonary alveolar:	n/a
3	chr10:61297420-61297470	HepG2	liver:	n/a
4	chr10:61297420-61297470	SKMC	muscle:	n/a
5	chr10:61297420-61297470	HUVEC	blood vessel:	n/a
6	chr10:61320994-61321044	SK-N-SH	brain:	n/a
7	chr10:61320994-61321044	HCF	heart:	n/a
8	chr10:61297420-61297470	Hela-S3	cervix:	n/a
9	chr10:61320994-61321044	SAEC	small airway:	n/a
10	chr10:61297420-61297470	ECC-1	luminal epithelium:	n/a
11	chr10:61320994-61321044	Caco-2	colon:	n/a
12	chr10:61320994-61321044	IMR90	lung:	fetal
13	chr10:61297420-61297470	HEK293	kidney:	embryo
14	chr10:61297420-61297470	A549	lung:	n/a
15	chr10:61320994-61321044	GM06990	blood:	n/a
16	chr10:61297420-61297470	NT2-D1	testis:	n/a
17	chr10:61320994-61321044	PFSK-1	brain:	n/a
18	chr10:61297420-61297470	SK-N-MC	brain:	n/a
19	chr10:61320994-61321044	NHBE	bronchial:	n/a
20	chr10:61297420-61297470	HAEpiC	amniotic membrane:	n/a
21	chr10:61297420-61297470	AG09309	skin:	n/a
22	chr10:61320994-61321044	NT2-D1	testis:	n/a
23	chr10:61297420-61297470	HMEC	breast:	n/a
24	chr10:61320994-61321044	SK-N-MC	brain:	n/a
25	chr10:61297420-61297470	HRE	kidney:	n/a
26	chr10:61297420-61297470	AG10803	skin:	n/a
27	chr10:61297420-61297470	SK-N-SH_RA	brain:	n/a
28	chr10:61297420-61297470	K562	blood:	n/a
29	chr10:61297420-61297470	MCF10A-Er-Src	breast:	n/a
30	chr10:61297420-61297470	PANC-1	pancreas:	n/a
31	chr10:61320994-61321044	HRPEpiC	eye:	n/a
32	chr10:61297420-61297470	GM12891	blood:	n/a
33	chr10:61320994-61321044	HMEC	breast:	n/a
34	chr10:61320994-61321044	PrEC	prostate:	n/a
35	chr10:61320994-61321044	GM12878	blood:	n/a
36	chr10:61297420-61297470	GM06990	blood:	n/a
37	chr10:61297420-61297470	HIPEpiC	eye:	n/a
38	chr10:61320994-61321044	HL-60	blood:	n/a
39	chr10:61297420-61297470	GM12878	blood:	n/a
40	chr10:61297420-61297470	BE2_C	brain:	n/a
41	chr10:61320994-61321044	HAEpiC	amniotic membrane:	n/a
42	chr10:61297420-61297470	SAEC	small airway:	n/a
43	chr10:61297420-61297470	AG04450	lung:	fetal
44	chr10:61320994-61321044	Hepatocyte	liver:	n/a
45	chr10:61320994-61321044	GM12892	blood:	n/a
46	chr10:61297420-61297470	PrEC	prostate:	n/a
47	chr10:61320994-61321044	HEEpiC	esophagus:	n/a
48	chr10:61297420-61297470	HRCEpiC	kidney:	n/a
49	chr10:61320994-61321044	RPTEC	kidney:	n/a
50	chr10:61320994-61321044	GM19239	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr10:61267850..61270399-chr10:61270512..61272281,2	MCF-7	breast:
2	chr10:61000034..61000606-chr10:61224554..61225057,2	MCF-7	breast:
3	chr10:61267850..61270399-chr10:61270512..61272281,2	MCF-7	breast:
4	chr10:61216355..61218212-chr10:61221634..61223150,2	K562	blood:
5	chr10:61271218..61273599-chr10:61281007..61283665,2	K562	blood:
6	chr10:61316394..61318901-chr10:61319114..61321714,2	K562	blood:
7	chr10:61316394..61318901-chr10:61319114..61321714,2	K562	blood:
8	chr10:61271218..61273599-chr10:61281007..61283665,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC16A9-4	chr10:61311162-61311636	NONHSAT013524

No data

Variant related genes	Relation type
MRPL50P4	TF binding region
MRPL50P4	CpG island

Extended variants
information (count: 2175 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:2175 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7099568	chr10:61220923-61220924	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs11006508	chr10:61220977-61220978	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs72810449	chr10:61220979-61220980	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs368150629	chr10:61221045-61221046	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs564523013	chr10:61221047-61221048	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs368538322	chr10:61221065-61221066	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs146537143	chr10:61221096-61221097	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs540596549	chr10:61221117-61221118	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs572363263	chr10:61221145-61221146	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs111287073	chr10:61221173-61221174	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs529971086	chr10:61221231-61221232	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs192950617	chr10:61221310-61221311	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs183849067	chr10:61221314-61221315	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs111380581	chr10:61221329-61221330	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs188190698	chr10:61221350-61221351	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs139083389	chr10:61221390-61221391	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs35760986	chr10:61221428-61221429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs530631043	chr10:61221448-61221449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs534334615	chr10:61221496-61221497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs142946864	chr10:61221557-61221558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs551606470	chr10:61221587-61221588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs568028314	chr10:61221613-61221614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs535809980	chr10:61221646-61221647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs111595760	chr10:61221648-61221649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs557627626	chr10:61221656-61221657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs551474705	chr10:61221742-61221743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs35875514	chr10:61221764-61221765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs1450770	chr10:61221780-61221781	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs180677887	chr10:61221798-61221799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183611690	chr10:61221842-61221843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549064207	chr10:61221860-61221861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs116890325	chr10:61221896-61221897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs540708416	chr10:61221907-61221908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562099250	chr10:61221915-61221916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs190794402	chr10:61221991-61221992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs541805552	chr10:61221993-61221994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs150378206	chr10:61221995-61221996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs530627709	chr10:61222004-61222005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs182010378	chr10:61222057-61222058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs187052837	chr10:61222097-61222098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs560514928	chr10:61222132-61222133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs191449734	chr10:61222159-61222160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs546275983	chr10:61222242-61222243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs568008455	chr10:61222251-61222252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs535380558	chr10:61222286-61222287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs16913629	chr10:61222287-61222288	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs569497368	chr10:61222306-61222307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs138068025	chr10:61222370-61222371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs149515534	chr10:61222380-61222381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs74337792	chr10:61222438-61222439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
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
Obesity	21956041	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
Metanephric adenoma	20802469	CNVD
Autism	20841430	CNVD
Prostate cancer	16573809	CNVD
Schizophrenia	19329560	CNVD
Heart failure	18772530	CNVD
Heart failure	18854381	CNVD
Hyperglycemia	19060297	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Usher syndrome	20538994	CNVD
Glioblastoma multiforme	17002787	CNVD
Urothelial carcinoma	21177765	CNVD
abnormal development	18461090	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
Myelofibrosis	22110671	CNVD
Epilepsy	20643615	CNVD
Neurodevelopmental disorder	22521361	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 myelogenous leukemia	20824076	CNVD
Papillary thyroid carcinoma	20824076	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:377 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:61215000-61221200	Weak transcription	Ovary	ovary
2	chr10:61216800-61222000	Weak transcription	HSMM	muscle
3	chr10:61220600-61221400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr10:61220800-61221400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr10:61221000-61221400	Enhancers	Fetal Stomach	stomach
6	chr10:61221200-61221400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr10:61221200-61221400	Enhancers	Ovary	ovary
8	chr10:61221400-61223400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr10:61221400-61223600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr10:61221400-61224800	Weak transcription	Ovary	ovary
11	chr10:61223600-61223800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr10:61223600-61224000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr10:61223600-61224000	Enhancers	Skeletal Muscle Female	skeletal muscle
14	chr10:61224600-61225200	Enhancers	Brain Substantia Nigra	brain
15	chr10:61224800-61225000	Enhancers	Ovary	ovary
16	chr10:61224800-61225000	Enhancers	HSMM	muscle
17	chr10:61230000-61230600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr10:61230400-61230800	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr10:61238800-61239400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr10:61239400-61239800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr10:61239400-61240400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr10:61241600-61241800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr10:61242800-61243000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr10:61251600-61252400	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr10:61252000-61252400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr10:61252000-61253200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr10:61252000-61253200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr10:61252200-61252400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr10:61252200-61252400	ZNF genes & repeats	Lung	lung
30	chr10:61252200-61252600	Enhancers	H1 Cell Line	embryonic stem cell
31	chr10:61252400-61253200	ZNF genes & repeats	Pancreas	Pancrea
32	chr10:61252600-61253000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr10:61253000-61253200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr10:61253000-61253400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr10:61253200-61255400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr10:61255400-61255600	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr10:61255400-61255600	ZNF genes & repeats	Fetal Lung	lung
38	chr10:61259800-61260400	Enhancers	Pancreatic Islets	Pancreatic Islet
39	chr10:61263400-61265000	Enhancers	Fetal Stomach	stomach
40	chr10:61264600-61268000	Weak transcription	Esophagus	oesophagus
41	chr10:61266200-61266600	Enhancers	HSMMtube	muscle
42	chr10:61268000-61268200	Enhancers	HMEC	breast
43	chr10:61268000-61268400	Enhancers	Esophagus	oesophagus
44	chr10:61272600-61272800	Enhancers	Colon Smooth Muscle	Colon
45	chr10:61272800-61274000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr10:61273200-61275000	Weak transcription	Colon Smooth Muscle	Colon
47	chr10:61274000-61275000	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr10:61274000-61276800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr10:61274200-61275000	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr10:61274200-61275000	Enhancers	iPS-15b Cell Line	embryonic stem cell

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