Variant report

Variant	esv996963
Chromosome Location	chr3:194845436-194854988
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:283)
CpG islands
(count:61)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:283 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:194850318-194850545	K562	blood:	n/a	n/a
2	ATF2	chr3:194854155-194854632	GM12878	blood:	n/a	n/a
3	ATF2	chr3:194849658-194851363	GM12878	blood:	n/a	n/a
4	ATF2	chr3:194849600-194851209	GM12878	blood:	n/a	n/a
5	ATF3	chr3:194854213-194854549	GM12878	blood:	n/a	n/a
6	BATF	chr3:194850078-194851099	GM12878	blood:	n/a	n/a
7	BATF	chr3:194854134-194854491	GM12878	blood:	n/a	chr3:194854300-194854311 chr3:194854305-194854315
8	BATF	chr3:194850186-194850676	GM12878	blood:	n/a	n/a
9	BCL11A	chr3:194850255-194850696	GM12878	blood:	n/a	n/a
10	BCL11A	chr3:194850114-194850772	GM12878	blood:	n/a	n/a
11	BCL3	chr3:194849761-194851147	GM12878	blood:	n/a	n/a
12	BCL3	chr3:194850097-194850953	GM12878	blood:	n/a	n/a
13	BCLAF1	chr3:194849741-194851217	GM12878	blood:	n/a	n/a
14	BCLAF1	chr3:194850040-194851010	GM12878	blood:	n/a	n/a
15	BHLHE40	chr3:194854303-194854489	GM12878	blood:	n/a	n/a
16	BHLHE40	chr3:194849877-194850840	GM12878	blood:	n/a	n/a
17	BRCA1	chr3:194850389-194850850	GM12878	blood:	n/a	n/a
18	CEBPB	chr3:194849985-194850506	IMR90	lung:	n/a	n/a
19	CEBPB	chr3:194849958-194849990	K562	blood:	n/a	n/a
20	CEBPB	chr3:194850223-194850666	GM12878	blood:	n/a	n/a
21	CEBPB	chr3:194849535-194851100	GM12878	blood:	n/a	n/a
22	CHD1	chr3:194849465-194851428	GM12878	blood:	n/a	n/a
23	CHD2	chr3:194849711-194851187	GM12878	blood:	n/a	n/a
24	CREB1	chr3:194850096-194850886	GM12878	blood:	n/a	n/a
25	CREB1	chr3:194854075-194854814	GM12878	blood:	n/a	n/a
26	CREB1	chr3:194854165-194854641	GM12878	blood:	n/a	n/a
27	CTCF	chr3:194854311-194854642	IMR90	lung:	n/a	n/a
28	CTCF	chr3:194854366-194854534	ProgFib	skin:	n/a	n/a
29	CTCF	chr3:194854361-194854546	LNCaP	prostate:	n/a	n/a
30	CTCF	chr3:194854434-194854495	Medullo	brain:	n/a	n/a
31	CTCF	chr3:194854318-194854574	NHEK	skin:	n/a	n/a
32	CTCF	chr3:194854423-194854529	K562	blood:	n/a	n/a
33	CTCF	chr3:194854384-194854506	Spleen_OC	spleen:	n/a	n/a
34	CTCF	chr3:194850371-194850582	GM12878	blood:	n/a	n/a
35	CTCF	chr3:194854422-194854431	Medullo	brain:	n/a	n/a
36	CTCF	chr3:194854414-194854505	K562	blood:	n/a	n/a
37	CTCF	chr3:194854380-194854530	NHEK	skin:	n/a	n/a
38	CTCF	chr3:194854380-194854530	BE2_C	brain:	n/a	n/a
39	CTCF	chr3:194854400-194854550	GM06990	blood:	n/a	n/a
40	CTCF	chr3:194854402-194854486	GM12892	blood:	n/a	n/a
41	CTCF	chr3:194854337-194854554	Fibrobl	skin:	n/a	n/a
42	CTCF	chr3:194854380-194854530	HPF	lung:	n/a	n/a
43	CTCF	chr3:194854408-194854496	GM19238	blood:	n/a	n/a
44	CTCF	chr3:194845440-194845590	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr3:194854389-194854477	Pancreas_OC	pancreas:	n/a	n/a
46	CTCF	chr3:194854340-194854490	HMF	breast:	n/a	n/a
47	CTCF	chr3:194854400-194854550	GM12873	blood:	n/a	n/a
48	CTCF	chr3:194854460-194854610	BE2_C	brain:	n/a	n/a
49	CTCF	chr3:194854323-194854577	GM12878	blood:	n/a	n/a
50	CTCF	chr3:194854320-194854470	AG10803	skin:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:194854342-194854392	Hela-S3	cervix:	n/a
2	chr3:194854342-194854392	ProgFib	skin:	n/a
3	chr3:194854342-194854392	BJ	skin:	n/a
4	chr3:194854342-194854392	HCPEpiC	choroid plexus:	n/a
5	chr3:194854342-194854392	HRPEpiC	eye:	n/a
6	chr3:194854342-194854392	Caco-2	colon:	n/a
7	chr3:194854342-194854392	HepG2	liver:	n/a
8	chr3:194854342-194854392	MCF-7	breast:	n/a
9	chr3:194854342-194854392	HCM	heart:	n/a
10	chr3:194854342-194854392	ovcar-3	ovarian:	n/a
11	chr3:194854342-194854392	NHDF-neo	bronchial:	n/a
12	chr3:194854342-194854392	AG09319	gingival:	n/a
13	chr3:194854342-194854392	AG09309	skin:	n/a
14	chr3:194854342-194854392	PANC-1	pancreas:	n/a
15	chr3:194854342-194854392	HRCEpiC	kidney:	n/a
16	chr3:194854342-194854392	LNCaP	prostate:	n/a
17	chr3:194854342-194854392	HNPCEpiC	eye:	n/a
18	chr3:194854342-194854392	HPAEpiC	pulmonary alveolar:	n/a
19	chr3:194854342-194854392	GM19239	blood:	n/a
20	chr3:194854342-194854392	HCT-116	colon:	n/a
21	chr3:194854342-194854392	NT2-D1	testis:	n/a
22	chr3:194854342-194854392	NB4	blood:	n/a
23	chr3:194854342-194854392	HRE	kidney:	n/a
24	chr3:194854342-194854392	CMK	blood:	n/a
25	chr3:194854342-194854392	A549	lung:	n/a
26	chr3:194854342-194854392	BE2_C	brain:	n/a
27	chr3:194854342-194854392	HCF	heart:	n/a
28	chr3:194854342-194854392	H1-hESC	embryonic stem cell:	embryo
29	chr3:194854342-194854392	NH-A	brain:	n/a
30	chr3:194854342-194854392	NHBE	bronchial:	n/a
31	chr3:194854342-194854392	U87	brain:	n/a
32	chr3:194854342-194854392	HEEpiC	esophagus:	n/a
33	chr3:194854342-194854392	AoSMC	blood vessel:	n/a
34	chr3:194854342-194854392	HL-60	blood:	n/a
35	chr3:194854342-194854392	AG04449	skin:	fetal
36	chr3:194854342-194854392	ECC-1	luminal epithelium:	n/a
37	chr3:194854342-194854392	HUVEC	blood vessel:	n/a
38	chr3:194854342-194854392	MCF10A-Er-Src	breast:	n/a
39	chr3:194854342-194854392	K562	blood:	n/a
40	chr3:194854342-194854392	SK-N-MC	brain:	n/a
41	chr3:194854342-194854392	AG10803	skin:	n/a
42	chr3:194854342-194854392	SAEC	small airway:	n/a
43	chr3:194854342-194854392	HEK293	kidney:	embryo
44	chr3:194854342-194854392	AG04450	lung:	fetal
45	chr3:194854342-194854392	HIPEpiC	eye:	n/a
46	chr3:194854342-194854392	GM12892	blood:	n/a
47	chr3:194854342-194854392	SK-N-SH_RA	brain:	n/a
48	chr3:194854342-194854392	PrEC	prostate:	n/a
49	chr3:194854342-194854392	GM12891	blood:	n/a
50	chr3:194854342-194854392	PFSK-1	brain:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:194850925..194853976-chr3:194854035..194858487,4	K562	blood:
2	chr3:194843365..194845377-chr3:194846362..194848480,3	MCF-7	breast:
3	chr3:194846812..194848589-chr3:194850352..194852170,2	K562	blood:
4	chr3:194846812..194848589-chr3:194850352..194852170,2	K562	blood:
5	chr3:194839189..194844993-chr3:194846673..194851288,6	K562	blood:
6	chr3:194843338..194845885-chr3:194853266..194854895,2	K562	blood:
7	chr3:194845075..194847856-chr3:194862075..194863679,2	K562	blood:
8	chr3:194843901..194846480-chr3:194857384..194859853,2	MCF-7	breast:
9	chr3:194851287..194852978-chr3:194986422..194989063,2	K562	blood:
10	chr3:194838089..194840730-chr3:194851941..194853573,2	K562	blood:
11	chr3:194844833..194847552-chr3:194858223..194860108,2	K562	blood:
12	chr3:194843338..194845885-chr3:194853266..194854895,2	K562	blood:
13	chr3:194849005..194851034-chr3:194888966..194890875,2	K562	blood:
14	chr3:194840845..194843057-chr3:194847738..194850410,3	MCF-7	breast:
15	chr3:194840263..194842347-chr3:194843295..194846088,2	MCF-7	breast:
16	chr3:194850288..194852181-chr3:194862414..194864990,2	MCF-7	breast:

No data

Variant related genes	Relation type
XXYLT1	TF binding region
XXYLT1	CpG island
ENSG00000265333	chromatin interactions
ENSG00000173950	chromatin interactions

Extended variants
information (count: 416 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:416 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555341155	chr3:194845449-194845450	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs79953661	chr3:194845483-194845484	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs534086381	chr3:194845492-194845493	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs559116663	chr3:194845522-194845523	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs371338885	chr3:194845525-194845526	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs577632503	chr3:194845558-194845559	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs544728871	chr3:194845591-194845592	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs556519607	chr3:194845626-194845627	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs143111209	chr3:194845635-194845636	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs369419528	chr3:194845644-194845645	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs542508121	chr3:194845682-194845683	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs147471973	chr3:194845690-194845691	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs528392574	chr3:194845736-194845737	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs375972342	chr3:194845751-194845752	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs73062325	chr3:194845796-194845797	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs184845490	chr3:194845798-194845799	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs189307597	chr3:194845799-194845800	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs551127827	chr3:194845819-194845820	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs73890687	chr3:194845820-194845821	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs530165828	chr3:194845876-194845877	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs528391681	chr3:194845910-194845911	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs536336318	chr3:194845942-194845943	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs77197763	chr3:194845987-194845988	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs569691341	chr3:194846007-194846008	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs567155387	chr3:194846028-194846029	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs534524654	chr3:194846029-194846030	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs558858710	chr3:194846046-194846047	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs375926253	chr3:194846062-194846063	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs180970862	chr3:194846093-194846094	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs58434965	chr3:194846096-194846097	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs184948614	chr3:194846097-194846098	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs577434773	chr3:194846147-194846148	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs371907851	chr3:194846182-194846183	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs574996035	chr3:194846183-194846184	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs535803452	chr3:194846190-194846191	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs554562650	chr3:194846202-194846203	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs73206646	chr3:194846219-194846220	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs540547220	chr3:194846222-194846223	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs191508879	chr3:194846235-194846236	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs376288959	chr3:194846237-194846238	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs529269302	chr3:194846269-194846270	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs114621069	chr3:194846285-194846286	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs551083286	chr3:194846294-194846295	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs562924533	chr3:194846304-194846305	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs141290370	chr3:194846322-194846323	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs375096517	chr3:194846323-194846324	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs368923540	chr3:194846327-194846328	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs575135428	chr3:194846329-194846330	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs527958246	chr3:194846371-194846372	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs76344236	chr3:194846378-194846379	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
Autism	19653912	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Cervical cancer	21062161	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Austim spectrum disorder	21302340	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	16397240	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
speech impairment	20736978	CNVD
Intracranial aneurysm	16715129	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mental retardation	17124404	CNVD
Congenital anomalies of the kidney and urinary tract	20299530	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21509527	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	16760732	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	22958593	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20970697	CNVD
Mental retardation	19951919	CNVD
Autism	20970697	CNVD
Developmental delay	18471269	CNVD
Intellectual disability	22045946	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Uveal melanoma	20484589	CNVD
3q29 microdeletion syndrome	20500065	CNVD
Biliary cancer	20453639	CNVD
3q29 microdeletion syndrome	22283845	CNVD
3q29 microdeletion syndrome	21626679	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Autosomal-dominant optic trophy	21036400	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:290 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:194822000-194846600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr3:194827400-194853600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr3:194827400-194861200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr3:194831600-194857400	Weak transcription	Pancreas	Pancrea
5	chr3:194832400-194853600	Weak transcription	Stomach Smooth Muscle	stomach
6	chr3:194832800-194856200	Weak transcription	Primary T cells from cord blood	blood
7	chr3:194834800-194850400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr3:194836000-194846200	Enhancers	Placenta	Placenta
9	chr3:194839200-194861200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr3:194839200-194861400	Weak transcription	Aorta	Aorta
11	chr3:194839400-194848800	Weak transcription	Lung	lung
12	chr3:194839600-194849200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr3:194840200-194849200	Weak transcription	Fetal Kidney	kidney
14	chr3:194840400-194846000	Weak transcription	Adipose Nuclei	Adipose
15	chr3:194840600-194849200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr3:194841000-194845800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr3:194841000-194849800	Weak transcription	NHLF	lung
18	chr3:194841000-194853400	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr3:194841000-194872800	Weak transcription	HSMMtube	muscle
20	chr3:194841400-194849000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr3:194841400-194868800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr3:194841800-194851200	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr3:194842600-194846000	Weak transcription	Thymus	Thymus
24	chr3:194842600-194846200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr3:194842800-194846200	Enhancers	Fetal Muscle Leg	muscle
26	chr3:194843200-194846600	Enhancers	Fetal Muscle Trunk	muscle
27	chr3:194843400-194846400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr3:194843400-194846400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr3:194843600-194846200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr3:194843800-194856600	Weak transcription	Monocytes-CD14+_RO01746	blood
31	chr3:194844000-194846200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr3:194844000-194847600	Enhancers	Primary hematopoietic stem cells	blood
33	chr3:194844200-194846400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr3:194844200-194846800	Weak transcription	Spleen	Spleen
35	chr3:194844200-194849000	Weak transcription	Dnd41	blood
36	chr3:194844400-194845600	Enhancers	Skeletal Muscle Female	skeletal muscle
37	chr3:194844400-194848800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr3:194844400-194849800	Weak transcription	NHDF-Ad	bronchial
39	chr3:194844600-194846000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr3:194844600-194846600	Enhancers	HepG2	liver
41	chr3:194844600-194849400	Weak transcription	K562	blood
42	chr3:194844600-194860000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr3:194844800-194846200	Enhancers	Fetal Heart	heart
44	chr3:194844800-194846600	Enhancers	HUVEC	blood vessel
45	chr3:194844800-194847600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr3:194844800-194848000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr3:194844800-194848000	Enhancers	Fetal Thymus	thymus
48	chr3:194844800-194859800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr3:194845000-194845600	Enhancers	Fetal Intestine Small	intestine
50	chr3:194845000-194846400	Genic enhancers	Primary hematopoietic stem cells short term culture	blood

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