Variant report

Variant	nsv3591
Chromosome Location	chr22:30344208-30388897
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:262)
CpG islands
(count:0)
Chromatin interactive
region (count:40)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:262 , 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	chr22:30347797-30348766	K562	blood:	n/a	n/a
2	ARID3A	chr22:30363852-30363917	HepG2	liver:	n/a	n/a
3	ARID3A	chr22:30350226-30350571	K562	blood:	n/a	n/a
4	ATF1	chr22:30350281-30350497	K562	blood:	n/a	n/a
5	BCL3	chr22:30350255-30350578	GM12878	blood:	n/a	n/a
6	BCL3	chr22:30351966-30352212	GM12878	blood:	n/a	n/a
7	BCL3	chr22:30351926-30352244	GM12878	blood:	n/a	n/a
8	BHLHE40	chr22:30348005-30348450	K562	blood:	n/a	n/a
9	BHLHE40	chr22:30350297-30350667	K562	blood:	n/a	chr22:30350654-30350667 chr22:30350656-30350665 chr22:30350656-30350665
10	CCNT2	chr22:30348042-30348819	K562	blood:	n/a	chr22:30348262-30348282
11	CEBPB	chr22:30384751-30385106	HepG2	liver:	n/a	n/a
12	CEBPB	chr22:30350430-30350453	IMR90	lung:	n/a	n/a
13	CEBPB	chr22:30384628-30385067	A549	lung:	n/a	n/a
14	CEBPB	chr22:30350241-30350573	K562	blood:	n/a	n/a
15	CEBPB	chr22:30384793-30385074	A549	lung:	n/a	n/a
16	CEBPB	chr22:30384797-30385044	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr22:30347970-30348719	K562	blood:	n/a	n/a
18	CEBPB	chr22:30384125-30384152	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr22:30384776-30385076	K562	blood:	n/a	n/a
20	CEBPB	chr22:30352005-30352254	MCF-7	breast:	n/a	chr22:30352135-30352146 chr22:30352133-30352146
21	CEBPB	chr22:30384743-30385103	IMR90	lung:	n/a	n/a
22	CEBPB	chr22:30351709-30351868	K562	blood:	n/a	n/a
23	CEBPB	chr22:30352046-30352234	HepG2	liver:	n/a	chr22:30352135-30352146 chr22:30352133-30352146
24	CEBPB	chr22:30384033-30384245	K562	blood:	n/a	n/a
25	CEBPB	chr22:30370940-30371009	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr22:30344613-30344652	IMR90	lung:	n/a	n/a
27	CEBPB	chr22:30352024-30352234	Hela-S3	cervix:	n/a	chr22:30352135-30352146 chr22:30352133-30352146
28	CEBPB	chr22:30371568-30371787	HepG2	liver:	n/a	chr22:30371645-30371656
29	CEBPB	chr22:30350269-30350618	K562	blood:	n/a	n/a
30	CEBPB	chr22:30371587-30371746	A549	lung:	n/a	chr22:30371645-30371656
31	CEBPB	chr22:30347901-30348464	K562	blood:	n/a	n/a
32	CEBPB	chr22:30384801-30385089	MCF-7	breast:	n/a	n/a
33	CEBPB	chr22:30384785-30384953	HepG2	liver:	n/a	n/a
34	CEBPB	chr22:30351996-30352267	IMR90	lung:	n/a	chr22:30352135-30352146 chr22:30352133-30352146
35	CEBPB	chr22:30371521-30371774	H1-hESC	embryonic stem cell:	n/a	chr22:30371645-30371656
36	CEBPB	chr22:30371567-30371743	IMR90	lung:	n/a	chr22:30371645-30371656
37	CEBPD	chr22:30347977-30348593	K562	blood:	n/a	n/a
38	CEBPD	chr22:30347982-30348604	K562	blood:	n/a	n/a
39	CTCF	chr22:30362580-30362730	MCF-7	breast:	n/a	n/a
40	CTCF	chr22:30362600-30362750	AG04450	lung:	n/a	n/a
41	CTCF	chr22:30362640-30362790	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr22:30362560-30362710	HPF	lung:	n/a	n/a
43	CTCF	chr22:30362660-30362810	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr22:30344964-30344985	GM20000	blood:	n/a	n/a
45	CTCF	chr22:30362686-30362745	GM12878	blood:	n/a	n/a
46	CTCF	chr22:30362660-30362810	GM12874	blood:	n/a	n/a
47	CTCF	chr22:30362660-30362810	HEEpiC	esophagus:	n/a	n/a
48	CTCF	chr22:30362640-30362790	GM12868	blood:	n/a	n/a
49	CTCF	chr22:30362692-30362697	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr22:30362700-30362757	A549	lung:	n/a	n/a

No data

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr22:30381816..30383716-chr22:30385807..30388025,2	K562	blood:
2	chr22:30366853..30371460-chr22:30371891..30375827,4	MCF-7	breast:
3	chr22:30387371..30390104-chr22:30390840..30392967,2	MCF-7	breast:
4	chr22:30308576..30310461-chr22:30376998..30379736,2	K562	blood:
5	chr22:30277883..30280870-chr22:30367706..30370340,3	K562	blood:
6	chr22:30162215..30164078-chr22:30387745..30390340,2	MCF-7	breast:
7	chr22:30354232..30357040-chr22:30359607..30363424,3	MCF-7	breast:
8	chr22:30369409..30372830-chr22:30374993..30377919,3	MCF-7	breast:
9	chr22:30277883..30280606-chr22:30367706..30369790,2	K562	blood:
10	chr22:30362170..30364148-chr22:30364525..30367430,3	K562	blood:
11	chr22:30388182..30391432-chr22:30393585..30396816,3	K562	blood:
12	chr22:30381816..30383716-chr22:30385807..30388025,2	K562	blood:
13	chr22:30353123..30354651-chr22:30355754..30358455,2	MCF-7	breast:
14	chr22:30346859..30350735-chr22:30351458..30355335,4	K562	blood:
15	chr22:30363254..30365949-chr22:30378819..30380914,2	K562	blood:
16	chr22:30368906..30371469-chr22:30373456..30376655,3	K562	blood:
17	chr22:30353695..30355711-chr22:30356514..30358241,2	MCF-7	breast:
18	chr22:30365436..30368018-chr22:30369958..30371760,2	K562	blood:
19	chr22:30362158..30363742-chr22:30364896..30367114,2	K562	blood:
20	chr22:30349519..30352332-chr22:30354507..30356583,2	MCF-7	breast:
21	chr22:30096098..30098972-chr22:30384609..30387065,2	MCF-7	breast:
22	chr22:30372068..30374181-chr22:30380564..30382189,2	K562	blood:
23	chr22:30353123..30354651-chr22:30355754..30358455,2	MCF-7	breast:
24	chr22:30372712..30375729-chr22:30378749..30380961,3	MCF-7	breast:
25	chr22:30348834..30351665-chr22:30352625..30356782,4	K562	blood:
26	chr22:30369409..30372830-chr22:30374993..30377919,3	MCF-7	breast:
27	chr22:30330994..30332769-chr22:30343214..30346064,2	MCF-7	breast:
28	chr22:30376984..30378787-chr22:30386876..30389530,2	MCF-7	breast:
29	chr22:30349519..30352332-chr22:30354507..30356583,2	MCF-7	breast:
30	chr22:30366853..30371460-chr22:30371891..30375827,4	MCF-7	breast:
31	chr22:30388710..30391580-chr22:30397983..30401344,3	MCF-7	breast:
32	chr22:30363254..30365949-chr22:30378819..30380914,2	K562	blood:
33	chr22:30368906..30372309-chr22:30373836..30377442,4	K562	blood:
34	chr22:30348834..30351665-chr22:30352625..30356782,4	K562	blood:
35	chr22:30388182..30392809-chr22:30393222..30398050,6	K562	blood:
36	chr22:30353695..30355711-chr22:30356514..30358241,2	MCF-7	breast:
37	chr22:30346859..30350735-chr22:30351458..30355335,4	K562	blood:
38	chr22:30354232..30357040-chr22:30359607..30363424,3	MCF-7	breast:
39	chr22:30376984..30378787-chr22:30386876..30389530,2	MCF-7	breast:
40	chr22:30231401..30237558-chr22:30387473..30391733,6	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HORMAD2-6	chr22:30374925-30374957	NONHSAT084740
2	lnc-ASCC2-1	chr22:30363672-30366965	ENSG00000249836
3	lnc-HORMAD2-6	chr22:30366965-30367051	NONHSAT084740
4	lnc-HORMAD2-6	chr22:30374414-30374520	NONHSAT084740
5	lnc-HORMAD2-6	chr22:30353025-30353077	NONHSAT084740

No data

Variant related genes	Relation type
MTMR3	TF binding region
ENSG00000100330	chromatin interactions
ENSG00000100319	chromatin interactions
ENSG00000100325	chromatin interactions
ENSG00000184076	chromatin interactions
MNX1	miRNA target sites

Extended variants
information (count: 1789 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:1789 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146435271	chr22:30344235-30344236	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs563944074	chr22:30344242-30344243	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs577453855	chr22:30344273-30344274	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs372116562	chr22:30344317-30344318	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs559987466	chr22:30344341-30344342	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs542245690	chr22:30344381-30344382	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs139025427	chr22:30344433-30344434	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs200426271	chr22:30344457-30344458	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs191655065	chr22:30344483-30344484	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs143781390	chr22:30344565-30344566	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs529951287	chr22:30344567-30344568	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs183482130	chr22:30344653-30344654	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs187051987	chr22:30344696-30344697	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs147220288	chr22:30344705-30344706	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs560730579	chr22:30344714-30344715	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs139601986	chr22:30344730-30344731	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs191694275	chr22:30344745-30344746	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs73162756	chr22:30344771-30344772	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs529765211	chr22:30344776-30344777	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs35433786	chr22:30344788-30344789	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs67687306	chr22:30344789-30344790	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs398121788	chr22:30344799-30344800	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs184286025	chr22:30344851-30344852	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs568903166	chr22:30344865-30344866	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs149302945	chr22:30344870-30344871	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs374098411	chr22:30344944-30344945	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs572800589	chr22:30345001-30345002	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs376205809	chr22:30345025-30345026	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs9625890	chr22:30345028-30345029	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs538455638	chr22:30345055-30345056	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553664241	chr22:30345070-30345071	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs111347032	chr22:30345082-30345083	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs9614114	chr22:30345132-30345133	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs34077534	chr22:30345136-30345137	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs575213389	chr22:30345180-30345181	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs542413871	chr22:30345185-30345186	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs368911457	chr22:30345186-30345187	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs371350118	chr22:30345191-30345192	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs563763677	chr22:30345195-30345196	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531011452	chr22:30345247-30345248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs186747172	chr22:30345274-30345275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs564495877	chr22:30345312-30345313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs375955791	chr22:30345326-30345327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs9625891	chr22:30345333-30345334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs144535590	chr22:30345374-30345375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs373892349	chr22:30345391-30345392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs546590599	chr22:30345399-30345400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs13058334	chr22:30345400-30345401	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs529164034	chr22:30345433-30345434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs56773543	chr22:30345434-30345435	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Velocardiofacial syndrome	20111667	CNVD
Medulloblastoma	21979893	CNVD
sporadic solitary meningiomas	19589153	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Congenital heart defect	22511896	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Seminomas	18059402	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Metachromatic leukodystrophy	18421352	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Breast cancer	21858162	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	22174824	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	21251322	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Lung cancer	18438408	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Cancer	21183584	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	19521646	CNVD
Schizophrenia	18990708	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	17322880	CNVD
Breast cancer	20409316	CNVD
Neurofibromatosis type 2	19566914	CNVD
Autism	19384346	CNVD
Melanoma	17363583	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1156 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:30313600-30354200	Weak transcription	Small Intestine	intestine
2	chr22:30328400-30351800	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr22:30332600-30345000	Weak transcription	Pancreas	Pancrea
4	chr22:30332600-30347400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr22:30334200-30374800	Weak transcription	Thymus	Thymus
6	chr22:30340000-30344800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr22:30340000-30345000	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr22:30340000-30345000	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr22:30340000-30346800	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr22:30340200-30351000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr22:30340200-30355400	Weak transcription	Fetal Intestine Small	intestine
12	chr22:30340200-30374800	Weak transcription	Fetal Thymus	thymus
13	chr22:30340600-30347400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
14	chr22:30340600-30347600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr22:30340600-30347600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr22:30340600-30360400	Weak transcription	Primary hematopoietic stem cells	blood
17	chr22:30340600-30370000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr22:30340600-30375000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
19	chr22:30340800-30350400	Weak transcription	Stomach Mucosa	stomach
20	chr22:30340800-30376000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr22:30341200-30345400	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr22:30341200-30352200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr22:30341200-30353600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr22:30341400-30344800	Weak transcription	Lung	lung
25	chr22:30341400-30346600	Weak transcription	Primary T cells fromperipheralblood	blood
26	chr22:30341400-30348000	Weak transcription	Primary neutrophils fromperipheralblood	blood
27	chr22:30341400-30351000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
28	chr22:30341400-30354400	Weak transcription	Rectal Mucosa Donor 29	rectum
29	chr22:30341400-30355200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr22:30341600-30344600	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr22:30341800-30347600	Weak transcription	Primary T helper cells fromperipheralblood	blood
32	chr22:30342000-30344600	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr22:30342000-30344600	Enhancers	Brain Substantia Nigra	brain
34	chr22:30342200-30344600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr22:30342200-30344600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr22:30342200-30345000	Enhancers	Brain Angular Gyrus	brain
37	chr22:30342200-30345200	Enhancers	Skeletal Muscle Male	skeletal muscle
38	chr22:30342400-30344800	Weak transcription	Left Ventricle	heart
39	chr22:30342600-30344800	Weak transcription	Ovary	ovary
40	chr22:30342600-30345000	Weak transcription	Psoas Muscle	Psoas
41	chr22:30342600-30345800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr22:30342600-30350400	Weak transcription	Aorta	Aorta
43	chr22:30342600-30350400	Weak transcription	Right Atrium	heart
44	chr22:30342600-30352200	Weak transcription	Gastric	stomach
45	chr22:30342600-30375200	Weak transcription	Spleen	Spleen
46	chr22:30342800-30344800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr22:30343000-30344600	Enhancers	Osteobl	bone
48	chr22:30343000-30344800	Enhancers	Duodenum Smooth Muscle	Duodenum
49	chr22:30343000-30345000	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr22:30343000-30345000	Enhancers	Brain Germinal Matrix	brain

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