Variant report

Variant	nsv524432
Chromosome Location	chr22:34119866-34146368
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	BACH1	chr22:34135101-34135251	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL3	chr22:34139772-34140140	GM12878	blood:	n/a	n/a
3	BHLHE40	chr22:34119934-34120194	GM12878	blood:	n/a	n/a
4	CEBPB	chr22:34142642-34142976	A549	lung:	n/a	chr22:34142745-34142756 chr22:34142744-34142757
5	CEBPB	chr22:34142598-34142923	HepG2	liver:	n/a	chr22:34142745-34142756 chr22:34142744-34142757
6	CEBPB	chr22:34142582-34142926	HepG2	liver:	n/a	chr22:34142745-34142756 chr22:34142744-34142757
7	CEBPB	chr22:34142695-34142833	HepG2	liver:	n/a	chr22:34142745-34142756 chr22:34142744-34142757
8	CTCF	chr22:34122620-34122770	AoAF	blood vessel:	n/a	n/a
9	CTCF	chr22:34143840-34143990	WERI-Rb-1	eye:	n/a	n/a
10	CTCF	chr22:34143900-34144050	MCF-7	breast:	n/a	chr22:34143994-34144010 chr22:34143988-34144009 chr22:34143993-34144011 chr22:34143995-34144008
11	CTCF	chr22:34144000-34144150	GM12878	blood:	n/a	n/a
12	CTCF	chr22:34133324-34133341	GM10266	blood:	n/a	n/a
13	CTCF	chr22:34122700-34122850	HepG2	liver:	n/a	n/a
14	CTCF	chr22:34143960-34144110	AoAF	blood vessel:	n/a	chr22:34143994-34144010 chr22:34143988-34144009 chr22:34143993-34144011 chr22:34143995-34144008
15	CTCF	chr22:34143900-34144050	RPTEC	kidney:	n/a	chr22:34143994-34144010 chr22:34143988-34144009 chr22:34143993-34144011 chr22:34143995-34144008
16	CTCF	chr22:34144060-34144210	GM12864	blood:	n/a	n/a
17	CTCF	chr22:34143880-34144030	HMF	breast:	n/a	chr22:34143994-34144010 chr22:34143988-34144009 chr22:34143993-34144011 chr22:34143995-34144008
18	CTCF	chr22:34143900-34144050	GM12873	blood:	n/a	chr22:34143994-34144010 chr22:34143988-34144009 chr22:34143993-34144011 chr22:34143995-34144008
19	CTCF	chr22:34143860-34144010	GM12873	blood:	n/a	chr22:34143994-34144010 chr22:34143988-34144009 chr22:34143995-34144008
20	CTCF	chr22:34122620-34122770	AG04450	lung:	n/a	n/a
21	CTCF	chr22:34143860-34144010	BJ	skin:	n/a	chr22:34143994-34144010 chr22:34143988-34144009 chr22:34143995-34144008
22	CTCF	chr22:34122600-34122750	HPF	lung:	n/a	n/a
23	CTCF	chr22:34143900-34144050	HPAF	blood vessel:	n/a	chr22:34143994-34144010 chr22:34143988-34144009 chr22:34143993-34144011 chr22:34143995-34144008
24	CTCF	chr22:34143880-34144030	SK-N-SH_RA	brain:	n/a	chr22:34143994-34144010 chr22:34143988-34144009 chr22:34143993-34144011 chr22:34143995-34144008
25	CTCF	chr22:34122660-34122810	NHLF	lung:	n/a	n/a
26	CTCF	chr22:34122620-34122770	HEK293	kidney:	n/a	n/a
27	CTCF	chr22:34143940-34144090	HRE	kidney:	n/a	chr22:34143994-34144010 chr22:34143988-34144009 chr22:34143993-34144011 chr22:34143995-34144008
28	CTCF	chr22:34143940-34144090	HEK293	kidney:	n/a	chr22:34143994-34144010 chr22:34143988-34144009 chr22:34143993-34144011 chr22:34143995-34144008
29	CTCF	chr22:34143840-34143990	HEK293	kidney:	n/a	n/a
30	ELF1	chr22:34119930-34120284	GM12878	blood:	n/a	n/a
31	ELK1	chr22:34144735-34144984	GM12878	blood:	n/a	n/a
32	EP300	chr22:34144919-34144932	GM12878	blood:	n/a	n/a
33	FOXA2	chr22:34142602-34142863	HepG2	liver:	n/a	n/a
34	FOXA2	chr22:34142644-34142986	A549	lung:	n/a	n/a
35	GATA2	chr22:34125601-34125945	SH-SY5Y	brain:	n/a	n/a
36	GATA3	chr22:34145777-34145941	SH-SY5Y	brain:	n/a	n/a
37	GATA3	chr22:34123270-34123541	SH-SY5Y	brain:	n/a	n/a
38	JUN	chr22:34130194-34130203	HepG2	liver:	n/a	n/a
39	JUND	chr22:34143740-34143916	HepG2	liver:	n/a	chr22:34143887-34143896
40	JUND	chr22:34130090-34130220	HepG2	liver:	n/a	n/a
41	KAP1	chr22:34139070-34139349	HEK293	kidney:	n/a	n/a
42	MAFF	chr22:34124873-34125218	HepG2	liver:	n/a	chr22:34125184-34125198
43	MAFK	chr22:34124966-34125073	K562	blood:	n/a	n/a
44	MAFK	chr22:34124877-34125213	IMR90	lung:	n/a	chr22:34125181-34125201 chr22:34125184-34125198 chr22:34125183-34125199
45	MAFK	chr22:34124878-34125296	HepG2	liver:	n/a	chr22:34125181-34125201 chr22:34125184-34125198 chr22:34125183-34125199
46	MAFK	chr22:34127721-34127852	HepG2	liver:	n/a	n/a
47	MAFK	chr22:34124864-34125214	HepG2	liver:	n/a	chr22:34125181-34125201 chr22:34125184-34125198 chr22:34125183-34125199
48	MAX	chr22:34134351-34134551	H1-hESC	embryonic stem cell:	n/a	chr22:34134464-34134474
49	MAX	chr22:34119844-34120284	NB4	blood:	n/a	n/a
50	MYC	chr22:34119881-34120270	NB4	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr22:34143232..34145432-chr22:34315745..34318657,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TIMP3-6	chr22:34121000-34121087	NONHSAT085013
2	lnc-TIMP3-6	chr22:34122102-34122183	ENSG00000224973.1
3	lnc-TIMP3-6	chr22:34121003-34121087	NONHSAT085014
4	lnc-TIMP3-6	chr22:34140116-34140315	ENSG00000224973.1
5	lnc-TIMP3-6	chr22:34121598-34121742	NONHSAT085012
6	lnc-TIMP3-6	chr22:34140116-34140179	ENSG00000224973.1
7	lnc-TIMP3-6	chr22:34128267-34128635	NONHSAT085018
8	lnc-TIMP3-6	chr22:34133550-34133769	NONHSAT085011
9	lnc-TIMP3-6	chr22:34123477-34123618	ENSG00000224973.1
10	lnc-TIMP3-6	chr22:34121013-34121087	ENSG00000224973.1
11	lnc-TIMP3-6	chr22:34121000-34121087	ENSG00000224973.1
12	lnc-TIMP3-6	chr22:34121598-34121742	NONHSAT085011
13	lnc-TIMP3-6	chr22:34133550-34133769	ENSG00000224973.1
14	lnc-TIMP3-6	chr22:34143657-34143811	ENSG00000224973.1
15	lnc-TIMP3-6	chr22:34120972-34121087	NONHSAT085012
16	lnc-TIMP3-6	chr22:34123477-34123574	ENSG00000224973.1
17	lnc-TIMP3-6	chr22:34133550-34133769	NONHSAT085013
18	lnc-TIMP3-6	chr22:34128242-34129671	NONHSAT085011
19	lnc-TIMP3-6	chr22:34123477-34123618	ENSG00000224973.1
20	lnc-TIMP3-6	chr22:34123477-34123618	ENSG00000224973.1
21	lnc-TIMP3-6	chr22:34140116-34140315	ENSG00000224973.1
22	lnc-TIMP3-6	chr22:34142402-34142444	ENSG00000224973.1
23	lnc-TIMP3-6	chr22:34140116-34140315	NONHSAT085015
24	lnc-TIMP3-6	chr22:34142402-34142444	NONHSAT085012
25	lnc-TIMP3-6	chr22:34140116-34140315	NONHSAT085012
26	lnc-TIMP3-6	chr22:34143657-34143811	NONHSAT085011
27	lnc-SYN3-4	chr22:34119818-34120265	ENSG00000232081.1
28	lnc-TIMP3-6	chr22:34121055-34121087	ENSG00000224973.1
29	lnc-TIMP3-6	chr22:34122102-34122183	NONHSAT085011
30	lnc-TIMP3-6	chr22:34123477-34123618	NONHSAT085011
31	lnc-TIMP3-6	chr22:34128242-34129671	NONHSAT085013
32	lnc-TIMP3-6	chr22:34143657-34143811	NONHSAT085015
33	lnc-TIMP3-6	chr22:34120972-34121087	NONHSAT085011
34	lnc-TIMP3-6	chr22:34133550-34133769	NONHSAT085014
35	lnc-TIMP3-6	chr22:34121598-34121742	ENSG00000224973.1
36	lnc-TIMP3-6	chr22:34133550-34133769	NONHSAT085015
37	lnc-TIMP3-6	chr22:34122102-34122183	NONHSAT085015
38	lnc-TIMP3-6	chr22:34123477-34123618	NONHSAT085015
39	lnc-TIMP3-6	chr22:34142402-34142444	ENSG00000224973.1
40	lnc-TIMP3-6	chr22:34121598-34121742	NONHSAT085015
41	lnc-TIMP3-6	chr22:34123477-34123574	NONHSAT085013
42	lnc-TIMP3-6	chr22:34121058-34121087	ENSG00000224973.1
43	lnc-TIMP3-6	chr22:34121003-34121087	NONHSAT085015
44	lnc-SYN3-4	chr22:34120789-34120898	ENSG00000232081.1
45	lnc-TIMP3-6	chr22:34123477-34123618	ENSG00000224973.1
46	lnc-TIMP3-6	chr22:34122102-34122183	NONHSAT085013
47	lnc-TIMP3-6	chr22:34143657-34143811	ENSG00000224973.1
48	lnc-TIMP3-6	chr22:34128242-34128488	ENSG00000224973.1
49	lnc-TIMP3-6	chr22:34133550-34133769	NONHSAT085018
50	lnc-TIMP3-6	chr22:34123477-34123618	NONHSAT085012

Variant related genes	Relation type
LARGE-AS1	TF binding region
LARGE-IT1	TF binding region
ENSG00000133424	chromatin interactions
ENSG00000273082	chromatin interactions

Extended variants
information (count: 1203 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1203 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs239315	chr22:34119866-34119867	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs239316	chr22:34119898-34119899	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs28390333	chr22:34119915-34119916	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs16992886	chr22:34119923-34119924	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs550374213	chr22:34119933-34119934	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs570131093	chr22:34119950-34119951	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs77464706	chr22:34120004-34120005	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs552696807	chr22:34120019-34120020	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs566128007	chr22:34120021-34120022	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs535020811	chr22:34120032-34120033	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs554627137	chr22:34120065-34120066	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs73170549	chr22:34120089-34120090	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs377192170	chr22:34120143-34120144	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs145126583	chr22:34120147-34120148	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs239317	chr22:34120162-34120163	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs373797210	chr22:34120167-34120168	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs544743120	chr22:34120187-34120188	Weak transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs140584023	chr22:34120202-34120203	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
19	rs144484044	chr22:34120204-34120205	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs574386413	chr22:34120237-34120238	Weak transcription Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs373722519	chr22:34120308-34120309	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs549933208	chr22:34120312-34120313	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs560697032	chr22:34120335-34120336	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs183000197	chr22:34120353-34120354	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs115532151	chr22:34120377-34120378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs569340973	chr22:34120380-34120381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs239318	chr22:34120395-34120396	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs572092891	chr22:34120405-34120406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs548555665	chr22:34120412-34120413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs73170550	chr22:34120436-34120437	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs533901892	chr22:34120522-34120523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs552758479	chr22:34120545-34120546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs566187539	chr22:34120554-34120555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs553773902	chr22:34120555-34120556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs577370281	chr22:34120579-34120580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs187617451	chr22:34120596-34120597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs548584754	chr22:34120597-34120598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs239319	chr22:34120608-34120609	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs574450604	chr22:34120633-34120634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs143949265	chr22:34120706-34120707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs147670590	chr22:34120718-34120719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs111700036	chr22:34120744-34120745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs532429908	chr22:34120771-34120772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs569559561	chr22:34120815-34120816	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
45	rs538447473	chr22:34120816-34120817	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs558287420	chr22:34120818-34120819	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs571833262	chr22:34120894-34120895	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs142319599	chr22:34120976-34120977	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs189673934	chr22:34121039-34121040	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
50	rs574344401	chr22:34121042-34121043	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
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
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
Endometrioid adenocarcinoma	16974079	CNVD
Acute myeloid leukemia	20729466	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
Malignant fibrous histiocytomas	21085701	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19384346	CNVD
Myelofibrosis	22110671	CNVD
muscular dystrophy type 1D	21248746	CNVD
Leukoplakia	24403051	CNVD
Ovarian neoplasms	16753589	CNVD
Deafness	17160897	CNVD
Bipolar disorder	19114987	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Prostate cancer	22341455	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:34105600-34133400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr22:34110800-34120200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr22:34110800-34122200	Weak transcription	Aorta	Aorta
4	chr22:34111000-34121400	Weak transcription	Ovary	ovary
5	chr22:34111200-34146200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr22:34111800-34122000	Weak transcription	Fetal Stomach	stomach
7	chr22:34111800-34142800	Weak transcription	Fetal Intestine Small	intestine
8	chr22:34116400-34135800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr22:34116800-34122200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr22:34117000-34120000	Weak transcription	Gastric	stomach
11	chr22:34117000-34120000	Weak transcription	Pancreas	Pancrea
12	chr22:34117200-34127400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr22:34117400-34120000	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr22:34117400-34122400	Weak transcription	Liver	Liver
15	chr22:34118400-34120000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr22:34118400-34121600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr22:34118400-34121800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr22:34118400-34122400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr22:34118600-34121600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr22:34118800-34120200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr22:34118800-34120200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr22:34118800-34121600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr22:34118800-34121600	Enhancers	Right Ventricle	heart
24	chr22:34119000-34120000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr22:34119000-34120800	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr22:34119000-34122000	Weak transcription	Fetal Brain Female	brain
27	chr22:34119200-34122600	Enhancers	Fetal Heart	heart
28	chr22:34119600-34121200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr22:34119600-34121200	Enhancers	Spleen	Spleen
30	chr22:34119600-34121400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr22:34119600-34121400	Weak transcription	NHEK	skin
32	chr22:34119800-34120200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr22:34119800-34120400	Enhancers	GM12878-XiMat	blood
34	chr22:34119800-34120800	Enhancers	Brain Anterior Caudate	brain
35	chr22:34119800-34121400	Enhancers	Right Atrium	heart
36	chr22:34119800-34121600	Enhancers	Primary B cells from peripheral blood	blood
37	chr22:34119800-34121800	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr22:34119800-34124200	Enhancers	Skeletal Muscle Female	skeletal muscle
39	chr22:34119800-34124800	Enhancers	Left Ventricle	heart
40	chr22:34120000-34120200	Genic enhancers	Gastric	stomach
41	chr22:34120000-34120200	ZNF genes & repeats	Pancreas	Pancrea
42	chr22:34120000-34120200	Enhancers	Psoas Muscle	Psoas
43	chr22:34120000-34121400	Enhancers	H1 Cell Line	embryonic stem cell
44	chr22:34120000-34121600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr22:34120200-34120800	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr22:34120200-34121000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr22:34120200-34121000	Weak transcription	Pancreas	Pancrea
48	chr22:34120200-34121000	Weak transcription	Psoas Muscle	Psoas
49	chr22:34120200-34122600	Enhancers	Skeletal Muscle Male	skeletal muscle
50	chr22:34120200-34125600	Weak transcription	Gastric	stomach

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