Variant report

Variant	esv1851082
Chromosome Location	chr22:30253256-30294744
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	chr22:30267819-30267923	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr22:30279479-30279812	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCLAF1	chr22:30279600-30279919	GM12878	blood:	n/a	n/a
4	BHLHE40	chr22:30279106-30279791	K562	blood:	n/a	chr22:30279511-30279527
5	BHLHE40	chr22:30278918-30279151	GM12878	blood:	n/a	chr22:30279006-30279022 chr22:30279105-30279121
6	BRCA1	chr22:30279281-30279298	HepG2	liver:	n/a	n/a
7	BRCA1	chr22:30279225-30279344	GM12878	blood:	n/a	n/a
8	BRCA1	chr22:30279422-30279568	Hela-S3	cervix:	n/a	n/a
9	CCNT2	chr22:30278996-30279811	K562	blood:	n/a	chr22:30279052-30279061 chr22:30279470-30279479
10	CEBPB	chr22:30282656-30282856	HepG2	liver:	n/a	n/a
11	CEBPB	chr22:30256059-30256259	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr22:30291559-30291624	HepG2	liver:	n/a	chr22:30291581-30291592
13	CEBPB	chr22:30256004-30256325	HepG2	liver:	n/a	n/a
14	CEBPB	chr22:30256069-30256278	IMR90	lung:	n/a	n/a
15	CEBPB	chr22:30282643-30282930	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr22:30256049-30256284	A549	lung:	n/a	n/a
17	CEBPB	chr22:30279056-30279292	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr22:30291550-30291641	K562	blood:	n/a	chr22:30291581-30291592
19	CHD1	chr22:30279159-30279853	GM12878	blood:	n/a	chr22:30279597-30279607
20	CHD2	chr22:30275813-30276023	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr22:30278968-30279791	Hela-S3	cervix:	n/a	chr22:30279597-30279607
22	CHD2	chr22:30279008-30279955	GM12878	blood:	n/a	chr22:30279597-30279607
23	CHD2	chr22:30279277-30279413	K562	blood:	n/a	n/a
24	CHD2	chr22:30279226-30279565	HepG2	liver:	n/a	n/a
25	CREB1	chr22:30279307-30279629	A549	lung:	n/a	n/a
26	CTCF	chr22:30279760-30279910	HFF	foreskin:	n/a	n/a
27	CTCF	chr22:30279440-30279590	HMEC	breast:	n/a	chr22:30279520-30279538 chr22:30279526-30279539 chr22:30279523-30279532 chr22:30279523-30279536
28	CTCF	chr22:30281784-30281810	LNCaP	prostate:	n/a	n/a
29	CTCF	chr22:30279392-30279612	SK-N-SH_RA	brain:	n/a	chr22:30279520-30279538 chr22:30279526-30279539 chr22:30279523-30279532 chr22:30279523-30279536
30	CTCF	chr22:30279500-30279650	GM12872	blood:	n/a	chr22:30279520-30279538 chr22:30279526-30279539 chr22:30279523-30279532 chr22:30279523-30279536
31	CTCF	chr22:30256783-30256802	GM20000	blood:	n/a	n/a
32	CTCF	chr22:30279520-30279670	HVMF	connective:	n/a	chr22:30279520-30279538 chr22:30279526-30279539 chr22:30279523-30279532 chr22:30279523-30279536
33	CTCF	chr22:30273660-30273810	HMF	breast:	n/a	n/a
34	CTCF	chr22:30279440-30279590	HRPEpiC	eye:	n/a	chr22:30279520-30279538 chr22:30279526-30279539 chr22:30279523-30279532 chr22:30279523-30279536
35	CTCF	chr22:30281772-30281782	LNCaP	prostate:	n/a	n/a
36	CTCF	chr22:30279680-30279830	AG04449	skin:	n/a	n/a
37	CTCF	chr22:30279700-30279850	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr22:30279723-30279804	GM20000	blood:	n/a	n/a
39	CTCF	chr22:30279480-30279630	HAc	cerebellar:	n/a	chr22:30279520-30279538 chr22:30279526-30279539 chr22:30279523-30279532 chr22:30279523-30279536
40	CTCF	chr22:30279016-30279258	Spleen_OC	spleen:	n/a	n/a
41	CTCF	chr22:30273660-30273810	AG10803	skin:	n/a	n/a
42	CTCF	chr22:30279540-30279690	K562	blood:	n/a	n/a
43	CTCF	chr22:30279440-30279590	AG10803	skin:	n/a	chr22:30279520-30279538 chr22:30279526-30279539 chr22:30279523-30279532 chr22:30279523-30279536
44	CTCF	chr22:30279440-30279590	AG09319	gingival:	n/a	chr22:30279520-30279538 chr22:30279526-30279539 chr22:30279523-30279532 chr22:30279523-30279536
45	CTCF	chr22:30279440-30279590	HPAF	blood vessel:	n/a	chr22:30279520-30279538 chr22:30279526-30279539 chr22:30279523-30279532 chr22:30279523-30279536
46	CTCF	chr22:30279680-30279830	HPF	lung:	n/a	n/a
47	CTCF	chr22:30279460-30279610	AG04449	skin:	n/a	chr22:30279520-30279538 chr22:30279526-30279539 chr22:30279523-30279532 chr22:30279523-30279536
48	CTCF	chr22:30279340-30279490	HAc	cerebellar:	n/a	n/a
49	CTCF	chr22:30279540-30279690	AG04450	lung:	n/a	n/a
50	CTCF	chr22:30273760-30273910	GM12871	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:30277968-30278018	HRPEpiC	eye:	n/a
2	chr22:30277968-30278018	HRPEpiC	eye:	n/a
3	chr22:30279857-30279907	HEK293	kidney:	embryo
4	chr22:30279857-30279907	SK-N-MC	brain:	n/a
5	chr22:30277968-30278018	HNPCEpiC	eye:	n/a
6	chr22:30283578-30283628	U87	brain:	n/a
7	chr22:30277968-30278018	AG04450	lung:	fetal
8	chr22:30275995-30276045	NHBE	bronchial:	n/a
9	chr22:30279857-30279907	AG04450	lung:	fetal
10	chr22:30278994-30279044	PrEC	prostate:	n/a
11	chr22:30279241-30279291	GM19239	blood:	n/a
12	chr22:30279857-30279907	ECC-1	luminal epithelium:	n/a
13	chr22:30279922-30279972	HUVEC	blood vessel:	n/a
14	chr22:30279857-30279907	AG09309	skin:	n/a
15	chr22:30275995-30276045	HL-60	blood:	n/a
16	chr22:30278876-30278926	PFSK-1	brain:	n/a
17	chr22:30279318-30279368	HCT-116	colon:	n/a
18	chr22:30279318-30279368	K562	blood:	n/a
19	chr22:30278994-30279044	NHBE	bronchial:	n/a
20	chr22:30275268-30275318	PFSK-1	brain:	n/a
21	chr22:30279857-30279907	K562	blood:	n/a
22	chr22:30279241-30279291	HAEpiC	amniotic membrane:	n/a
23	chr22:30275268-30275318	Jurkat	blood:	n/a
24	chr22:30278994-30279044	GM12892	blood:	n/a
25	chr22:30278876-30278926	HRE	kidney:	n/a
26	chr22:30277391-30277441	ovcar-3	ovarian:	n/a
27	chr22:30279318-30279368	ovcar-3	ovarian:	n/a
28	chr22:30278994-30279044	CMK	blood:	n/a
29	chr22:30279857-30279907	U87	brain:	n/a
30	chr22:30279241-30279291	RPTEC	kidney:	n/a
31	chr22:30277968-30278018	GM12878	blood:	n/a
32	chr22:30279241-30279291	NT2-D1	testis:	n/a
33	chr22:30278876-30278926	NT2-D1	testis:	n/a
34	chr22:30278992-30279042	ProgFib	skin:	n/a
35	chr22:30275995-30276045	HEK293	kidney:	embryo
36	chr22:30279318-30279368	NHBE	bronchial:	n/a
37	chr22:30278876-30278926	AG04449	skin:	fetal
38	chr22:30279241-30279291	GM12892	blood:	n/a
39	chr22:30279241-30279291	AoSMC	blood vessel:	n/a
40	chr22:30278992-30279042	IMR90	lung:	fetal
41	chr22:30275995-30276045	HNPCEpiC	eye:	n/a
42	chr22:30278876-30278926	GM12891	blood:	n/a
43	chr22:30279241-30279291	CMK	blood:	n/a
44	chr22:30275995-30276045	GM19239	blood:	n/a
45	chr22:30275268-30275318	BE2_C	brain:	n/a
46	chr22:30279318-30279368	MCF-7	breast:	n/a
47	chr22:30279318-30279368	HRE	kidney:	n/a
48	chr22:30279318-30279368	AG09309	skin:	n/a
49	chr22:30278876-30278926	MCF-7	breast:	n/a
50	chr22:30278876-30278926	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr22:30229506..30231085-chr22:30279535..30281040,2	MCF-7	breast:
2	chr10:62193967..62194535-chr22:30279507..30280085,2	MCF-7	breast:
3	chr22:30277721..30280339-chr22:30399364..30402748,3	K562	blood:
4	chr22:30280125..30281940-chr22:30289079..30291294,2	MCF-7	breast:
5	chr22:30289517..30291568-chr22:30301427..30303381,2	K562	blood:
6	chr22:30265481..30267590-chr22:30272869..30274738,2	MCF-7	breast:
7	chr22:30208243..30210090-chr22:30279066..30280884,2	MCF-7	breast:
8	chr22:30269255..30271141-chr22:30271794..30273974,2	MCF-7	breast:
9	chr22:30232954..30235817-chr22:30277750..30279574,2	MCF-7	breast:
10	chr22:30234009..30236728-chr22:30254612..30257175,2	MCF-7	breast:
11	chr22:30266018..30267537-chr22:30271072..30273991,2	K562	blood:
12	chr22:30266018..30267537-chr22:30271072..30273991,2	K562	blood:
13	chr22:30288615..30290652-chr22:30302494..30304851,2	MCF-7	breast:
14	chr22:30267624..30270362-chr22:30273098..30276358,3	K562	blood:
15	chr22:30280125..30281940-chr22:30289079..30291294,2	MCF-7	breast:
16	chr22:30208644..30211473-chr22:30268127..30270343,2	MCF-7	breast:
17	chr22:30240391..30242312-chr22:30254416..30255969,2	MCF-7	breast:
18	chr22:30267624..30270362-chr22:30273098..30276358,3	K562	blood:
19	chr22:30269255..30271141-chr22:30271794..30273974,2	MCF-7	breast:
20	chr22:30265481..30267590-chr22:30272869..30274738,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HORMAD2-6	chr22:30279168-30279348	NONHSAT084740

Variant related genes	Relation type
MTMR3	TF binding region
MTMR3	CpG island
ENSG00000100325	chromatin interactions
ENSG00000100330	chromatin interactions

Extended variants
information (count: 1609 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:1609 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4993442	chr22:30253256-30253257	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs557254058	chr22:30253259-30253260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs533885987	chr22:30253321-30253322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs186720443	chr22:30253352-30253353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs573840152	chr22:30253372-30253373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs5844878	chr22:30253378-30253379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs386395186	chr22:30253383-30253384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs373836368	chr22:30253389-30253390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs370544565	chr22:30253400-30253401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs550857086	chr22:30253495-30253496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs374263906	chr22:30253526-30253527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561930422	chr22:30253537-30253538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs544352551	chr22:30253542-30253543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs13055474	chr22:30253569-30253570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs13055634	chr22:30253577-30253578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs142437777	chr22:30253611-30253612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs557660623	chr22:30253628-30253629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs368670047	chr22:30253650-30253651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs371459780	chr22:30253664-30253665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs564348471	chr22:30253691-30253692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs528517962	chr22:30253695-30253696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs540374112	chr22:30253749-30253750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs561739057	chr22:30253768-30253769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs529324237	chr22:30253779-30253780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs564609706	chr22:30253830-30253831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs550579898	chr22:30253831-30253832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs113144507	chr22:30253858-30253859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs111476703	chr22:30253859-30253860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs372147319	chr22:30253862-30253863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs564535312	chr22:30253898-30253899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs562774910	chr22:30253911-30253912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs191406242	chr22:30253933-30253934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs551564730	chr22:30253959-30253960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs566678392	chr22:30253962-30253963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs533873631	chr22:30254007-30254008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs549131776	chr22:30254064-30254065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs13055196	chr22:30254066-30254067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs184657797	chr22:30254067-30254068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs28379948	chr22:30254074-30254075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs537817273	chr22:30254154-30254155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs555900342	chr22:30254173-30254174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs9614084	chr22:30254175-30254176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs8142188	chr22:30254207-30254208	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
44	rs557925984	chr22:30254220-30254221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs573141396	chr22:30254312-30254313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs8140871	chr22:30254321-30254322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs62227986	chr22:30254328-30254329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs376672922	chr22:30254424-30254425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs181662789	chr22:30254558-30254559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs540314584	chr22:30254576-30254577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:961 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:30248400-30254600	Weak transcription	HSMMtube	muscle
2	chr22:30253000-30255200	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr22:30253000-30257200	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr22:30253000-30257200	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr22:30253200-30255200	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr22:30253200-30255200	Weak transcription	Primary neutrophils fromperipheralblood	blood
7	chr22:30255200-30255400	Weak transcription	Primary B cells from cord blood	blood
8	chr22:30255200-30255600	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr22:30255200-30255800	Enhancers	Primary neutrophils fromperipheralblood	blood
10	chr22:30255200-30258400	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr22:30255400-30256800	Enhancers	Primary B cells from cord blood	blood
12	chr22:30255600-30257400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
13	chr22:30255800-30256000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
14	chr22:30255800-30258000	Weak transcription	HSMMtube	muscle
15	chr22:30256000-30256400	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr22:30256000-30257600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr22:30256200-30256400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr22:30256400-30256800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
19	chr22:30256400-30257000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
20	chr22:30257000-30258200	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr22:30257000-30258200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr22:30257200-30257400	Enhancers	Fetal Heart	heart
23	chr22:30257200-30257600	Enhancers	HepG2	liver
24	chr22:30257200-30258400	Enhancers	Skeletal Muscle Female	skeletal muscle
25	chr22:30257200-30259200	Enhancers	Skeletal Muscle Male	skeletal muscle
26	chr22:30257400-30257600	Flanking Active TSS	Fetal Heart	heart
27	chr22:30257400-30258200	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr22:30257600-30258400	Enhancers	Fetal Heart	heart
29	chr22:30257600-30260800	Weak transcription	HepG2	liver
30	chr22:30258000-30258400	Enhancers	HSMMtube	muscle
31	chr22:30258200-30259200	Weak transcription	Primary neutrophils fromperipheralblood	blood
32	chr22:30258200-30267600	Weak transcription	Monocytes-CD14+_RO01746	blood
33	chr22:30258400-30263200	Weak transcription	Primary monocytes fromperipheralblood	blood
34	chr22:30258400-30263400	Weak transcription	Fetal Heart	heart
35	chr22:30258400-30263600	Weak transcription	Skeletal Muscle Female	skeletal muscle
36	chr22:30259200-30259400	Enhancers	Primary neutrophils fromperipheralblood	blood
37	chr22:30259200-30259800	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr22:30259800-30260000	Enhancers	Skeletal Muscle Male	skeletal muscle
39	chr22:30260000-30263400	Weak transcription	Skeletal Muscle Male	skeletal muscle
40	chr22:30260800-30261000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr22:30260800-30261400	Enhancers	HepG2	liver
42	chr22:30261200-30265800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr22:30263000-30263800	Enhancers	NHEK	skin
44	chr22:30263200-30263800	Enhancers	Primary monocytes fromperipheralblood	blood
45	chr22:30263200-30263800	Enhancers	HMEC	breast
46	chr22:30263200-30264400	Enhancers	Fetal Brain Female	brain
47	chr22:30263400-30264400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr22:30263400-30264400	Enhancers	Skeletal Muscle Male	skeletal muscle
49	chr22:30263400-30264600	Enhancers	Fetal Heart	heart
50	chr22:30263400-30265000	Enhancers	Fetal Brain Male	brain

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