Variant report

Variant	nsv964031
Chromosome Location	chr4:9629449-9764955
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1415)
CpG islands
(count:977)
Chromatin interactive
region (count:21)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1415 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:9705188-9705304	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:9764889-9764976	K562	blood:	n/a	n/a
3	ATF1	chr4:9693437-9693703	K562	blood:	n/a	n/a
4	ATF1	chr4:9758253-9758343	K562	blood:	n/a	n/a
5	ATF2	chr4:9764713-9765001	GM12878	blood:	n/a	n/a
6	BACH1	chr4:9689846-9689882	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr4:9661312-9661676	GM12878	blood:	n/a	n/a
8	BATF	chr4:9697635-9697868	GM12878	blood:	n/a	n/a
9	BATF	chr4:9709608-9710002	GM12878	blood:	n/a	n/a
10	BATF	chr4:9709684-9709950	GM12878	blood:	n/a	n/a
11	BATF	chr4:9637521-9637725	GM12878	blood:	n/a	n/a
12	BATF	chr4:9715614-9715953	GM12878	blood:	n/a	n/a
13	BATF	chr4:9661377-9661663	GM12878	blood:	n/a	n/a
14	BCL11A	chr4:9709736-9710003	GM12878	blood:	n/a	n/a
15	BCL11A	chr4:9693955-9694191	GM12878	blood:	n/a	n/a
16	BCL11A	chr4:9637557-9637806	GM12878	blood:	n/a	n/a
17	BCL11A	chr4:9661303-9661712	GM12878	blood:	n/a	n/a
18	BCL11A	chr4:9709714-9709970	GM12878	blood:	n/a	n/a
19	BCL3	chr4:9747263-9747923	GM12878	blood:	n/a	n/a
20	BCL3	chr4:9747374-9747670	GM12878	blood:	n/a	n/a
21	BHLHE40	chr4:9764795-9765105	HepG2	liver:	n/a	n/a
22	BHLHE40	chr4:9693347-9693648	GM12878	blood:	n/a	n/a
23	BHLHE40	chr4:9705121-9705321	K562	blood:	n/a	n/a
24	BHLHE40	chr4:9693184-9693740	K562	blood:	n/a	n/a
25	BHLHE40	chr4:9764726-9765039	K562	blood:	n/a	n/a
26	BHLHE40	chr4:9764736-9765042	GM12878	blood:	n/a	n/a
27	BHLHE40	chr4:9733756-9733953	K562	blood:	n/a	n/a
28	BHLHE40	chr4:9661297-9661608	HepG2	liver:	n/a	n/a
29	BHLHE40	chr4:9693135-9693538	HepG2	liver:	n/a	chr4:9693155-9693171
30	BHLHE40	chr4:9697620-9697865	HepG2	liver:	n/a	n/a
31	BHLHE40	chr4:9705080-9705313	GM12878	blood:	n/a	n/a
32	CBX3	chr4:9709655-9709945	K562	blood:	n/a	n/a
33	CCNT2	chr4:9693190-9693570	K562	blood:	n/a	n/a
34	CEBPB	chr4:9759118-9759224	K562	blood:	n/a	n/a
35	CEBPB	chr4:9720234-9720515	HepG2	liver:	n/a	chr4:9720327-9720338
36	CEBPB	chr4:9727679-9727879	HepG2	liver:	n/a	chr4:9727792-9727803 chr4:9727792-9727805
37	CEBPB	chr4:9629876-9630149	HepG2	liver:	n/a	chr4:9630037-9630048
38	CEBPB	chr4:9637488-9637693	HepG2	liver:	n/a	chr4:9637617-9637628
39	CEBPB	chr4:9720182-9720485	K562	blood:	n/a	chr4:9720327-9720338
40	CEBPB	chr4:9759045-9759325	A549	lung:	n/a	n/a
41	CEBPB	chr4:9639784-9639891	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr4:9759126-9759326	IMR90	lung:	n/a	n/a
43	CEBPB	chr4:9764821-9764973	K562	blood:	n/a	n/a
44	CEBPB	chr4:9725682-9725793	HepG2	liver:	n/a	n/a
45	CEBPB	chr4:9661262-9661447	K562	blood:	n/a	n/a
46	CEBPD	chr4:9712816-9713034	K562	blood:	n/a	n/a
47	CHD2	chr4:9764709-9764909	HepG2	liver:	n/a	n/a
48	CHD2	chr4:9705111-9705206	GM12878	blood:	n/a	n/a
49	CTCF	chr4:9705120-9705270	HA-sp	spinal cord:	n/a	chr4:9705234-9705244
50	CTCF	chr4:9659840-9659954	MCF-7	breast:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:9693312-9693362	HCM	heart:	n/a
2	chr4:9693312-9693362	HCM	heart:	n/a
3	chr4:9692836-9692886	NB4	blood:	n/a
4	chr4:9692836-9692886	AG09309	skin:	n/a
5	chr4:9693516-9693566	HEEpiC	esophagus:	n/a
6	chr4:9760019-9760069	AoSMC	blood vessel:	n/a
7	chr4:9760019-9760069	NB4	blood:	n/a
8	chr4:9760736-9760786	PANC-1	pancreas:	n/a
9	chr4:9760275-9760325	HCPEpiC	choroid plexus:	n/a
10	chr4:9707741-9707791	PANC-1	pancreas:	n/a
11	chr4:9693312-9693362	GM12892	blood:	n/a
12	chr4:9696916-9696966	PrEC	prostate:	n/a
13	chr4:9760275-9760325	CMK	blood:	n/a
14	chr4:9760275-9760325	HRPEpiC	eye:	n/a
15	chr4:9689364-9689414	GM12878	blood:	n/a
16	chr4:9661405-9661455	HRCEpiC	kidney:	n/a
17	chr4:9709042-9709092	LNCaP	prostate:	n/a
18	chr4:9760736-9760786	AG10803	skin:	n/a
19	chr4:9693764-9693814	Hepatocyte	liver:	n/a
20	chr4:9692836-9692886	H1-hESC	embryonic stem cell:	embryo
21	chr4:9653008-9653058	Caco-2	colon:	n/a
22	chr4:9661405-9661455	AG10803	skin:	n/a
23	chr4:9709042-9709092	BJ	skin:	n/a
24	chr4:9693329-9693379	HAEpiC	amniotic membrane:	n/a
25	chr4:9696916-9696966	Hela-S3	cervix:	n/a
26	chr4:9692836-9692886	HIPEpiC	eye:	n/a
27	chr4:9762166-9762216	Hepatocyte	liver:	n/a
28	chr4:9661422-9661472	NHDF-neo	bronchial:	n/a
29	chr4:9693764-9693814	GM12878	blood:	n/a
30	chr4:9693312-9693362	ECC-1	luminal epithelium:	n/a
31	chr4:9692836-9692886	PFSK-1	brain:	n/a
32	chr4:9760275-9760325	HRCEpiC	kidney:	n/a
33	chr4:9760019-9760069	GM12892	blood:	n/a
34	chr4:9661405-9661455	GM12891	blood:	n/a
35	chr4:9760736-9760786	GM12878	blood:	n/a
36	chr4:9760019-9760069	NH-A	brain:	n/a
37	chr4:9692836-9692886	GM06990	blood:	n/a
38	chr4:9653008-9653058	ProgFib	skin:	n/a
39	chr4:9760275-9760325	MCF10A-Er-Src	breast:	n/a
40	chr4:9693516-9693566	PFSK-1	brain:	n/a
41	chr4:9762166-9762216	HepG2	liver:	n/a
42	chr4:9653008-9653058	HRPEpiC	eye:	n/a
43	chr4:9653008-9653058	HIPEpiC	eye:	n/a
44	chr4:9689364-9689414	NB4	blood:	n/a
45	chr4:9693516-9693566	PrEC	prostate:	n/a
46	chr4:9696916-9696966	SKMC	muscle:	n/a
47	chr4:9693516-9693566	ECC-1	luminal epithelium:	n/a
48	chr4:9692836-9692886	AG10803	skin:	n/a
49	chr4:9653008-9653058	U87	brain:	n/a
50	chr4:9693312-9693362	ProgFib	skin:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:9764417..9765133-chr4:10016121..10017439,5	MCF-7	breast:
2	chr2:91816303..91817383-chr4:9764391..9765414,6	MCF-7	breast:
3	chr1:149221736..149225365-chr4:9763717..9766826,4	MCF-7	breast:
4	chr4:9704873..9705750-chr4:10016280..10017221,3	K562	blood:
5	chr1:149220703..149225113-chr4:9764948..9767069,4	MCF-7	breast:
6	chr4:9704779..9705714-chr4:10015117..10016069,5	MCF-7	breast:
7	chr4:9764792..9765537-chr4:9899989..9900954,5	MCF-7	breast:
8	chr2:91815162..91820044-chr4:9763391..9768700,25	MCF-7	breast:
9	chr4:9699934..9701585-chr4:10019007..10021805,2	K562	blood:
10	chr4:9763456..9766236-chr4:10014004..10016919,3	K562	blood:
11	chr4:9764445..9765327-chr4:10020033..10020988,3	K562	blood:
12	chr4:9764866..9765415-chr4:9928949..9929492,2	MCF-7	breast:
13	chr4:9761130..9763005-chr4:9988480..9990175,2	K562	blood:
14	chr4:9764370..9765339-chr4:10015197..10016013,4	MCF-7	breast:
15	chr4:9764428..9765300-chr4:10016550..10017565,3	K562	blood:
16	chr4:9764437..9765430-chr4:10020023..10020916,6	MCF-7	breast:
17	chr4:9705037..9705657-chr4:9778184..9778690,2	K562	blood:
18	chr2:91816443..91817305-chr4:9764390..9765414,6	MCF-7	breast:
19	chr4:9705013..9706114-chr4:10020117..10020881,3	MCF-7	breast:
20	chr4:9533415..9534346-chr4:9660887..9661684,2	MCF-7	breast:
21	chr4:9764793..9765717-chr4:10015113..10016017,3	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC2A9-6	chr4:9680180-9680546	l_2603_chr4:9680179-9682164_kidney
2	lnc-DRD5-16	chr4:9678932-9679558	NONHSAT095141
3	lnc-SLC2A9-1	chr4:9691882-9692319	XLOC_003881
4	lnc-SLC2A9-2	chr4:9693361-9693365	XLOC_003880
5	lnc-DRD5-15	chr4:9680112-9680551	l_2602_chr4:9680111-9682135_thyroid
6	lnc-SLC2A9-6	chr4:9681968-9682164	l_2603_chr4:9680179-9682164_kidney
7	lnc-SLC2A9-2	chr4:9682416-9682671	XLOC_003880
8	lnc-SLC2A9-1	chr4:9686325-9686330	XLOC_003881
9	lnc-DRD5-15	chr4:9681973-9682135	l_2602_chr4:9680111-9682135_thyroid

No data

Variant related genes	Relation type
FAM86MP	TF binding region
ENSG00000249563	TF binding region
ALG1L3P	TF binding region
ENPP7P11	TF binding region
OR7E35P	TF binding region
FAM86MP	CpG island
ENSG00000249563	CpG island
ALG1L3P	CpG island
ENPP7P11	CpG island
OR7E35P	CpG island
ENSG00000206737	chromatin interactions
ENSG00000109667	chromatin interactions
FBXW7	miRNA target sites

Extended variants
information (count: 8519 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:8519 , 50 per page) page: 1 2 3 4 5 6 7 ... 171

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571688294	chr4:9629467-9629468	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs559633882	chr4:9629490-9629491	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs7666466	chr4:9629503-9629504	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs28491253	chr4:9629512-9629513	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs112855960	chr4:9629515-9629516	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531756537	chr4:9629521-9629522	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs188570131	chr4:9629534-9629535	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs140582452	chr4:9629540-9629541	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs564926148	chr4:9629585-9629586	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs193118204	chr4:9629605-9629606	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs547436438	chr4:9629618-9629619	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs565940441	chr4:9629639-9629640	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs566217239	chr4:9629645-9629646	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs150460251	chr4:9629662-9629663	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs367918409	chr4:9629664-9629665	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs138256063	chr4:9629690-9629691	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs537733380	chr4:9629708-9629709	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs143553681	chr4:9629711-9629712	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs558310446	chr4:9629728-9629729	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs184305430	chr4:9629730-9629731	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs73802936	chr4:9629733-9629734	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs188556209	chr4:9629739-9629740	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs536897056	chr4:9629755-9629756	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs34548152	chr4:9629767-9629768	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs147161802	chr4:9629772-9629773	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs370906662	chr4:9629816-9629817	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs563478088	chr4:9629844-9629845	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs73082831	chr4:9629850-9629851	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs180919275	chr4:9629864-9629865	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs115616919	chr4:9629866-9629867	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs138689181	chr4:9629887-9629888	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs541142739	chr4:9629896-9629897	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs554855339	chr4:9629899-9629900	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559392278	chr4:9629903-9629904	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs530186159	chr4:9629904-9629905	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs548533305	chr4:9629912-9629913	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs570223646	chr4:9629919-9629920	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs183629286	chr4:9629940-9629941	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576538264	chr4:9629951-9629952	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs190640820	chr4:9629958-9629959	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs536748478	chr4:9629963-9629964	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs561605835	chr4:9629966-9629967	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs141292952	chr4:9629974-9629975	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201505163	chr4:9629976-9629977	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs570471408	chr4:9629983-9629984	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs144121494	chr4:9629985-9629986	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs558571399	chr4:9629994-9629995	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs187343011	chr4:9630006-9630007	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs553128431	chr4:9630008-9630009	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs115966027	chr4:9630014-9630015	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Sezary syndrome	18413736	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:543 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:9624800-9637600	Weak transcription	Brain Hippocampus Middle	brain
2	chr4:9626000-9631000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr4:9626800-9631200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr4:9627000-9639000	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr4:9627400-9630600	Weak transcription	Fetal Brain Female	brain
6	chr4:9627800-9634400	Weak transcription	Brain Anterior Caudate	brain
7	chr4:9628200-9630400	Strong transcription	Ovary	ovary
8	chr4:9628600-9630800	Weak transcription	Brain Angular Gyrus	brain
9	chr4:9629400-9630000	Strong transcription	Stomach Smooth Muscle	stomach
10	chr4:9630000-9631600	Weak transcription	Stomach Smooth Muscle	stomach
11	chr4:9630400-9632000	Weak transcription	Ovary	ovary
12	chr4:9634400-9639400	Enhancers	Fetal Thymus	thymus
13	chr4:9637800-9638800	Enhancers	Thymus	Thymus
14	chr4:9640800-9643000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr4:9643000-9643800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr4:9643200-9645800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr4:9643800-9644000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr4:9661200-9661400	Enhancers	Fetal Muscle Leg	muscle
19	chr4:9661200-9662200	Weak transcription	Fetal Thymus	thymus
20	chr4:9661400-9662600	Weak transcription	Fetal Muscle Leg	muscle
21	chr4:9662600-9662800	Enhancers	Fetal Muscle Leg	muscle
22	chr4:9662800-9663400	Weak transcription	Fetal Muscle Leg	muscle
23	chr4:9663400-9663600	Enhancers	Fetal Muscle Leg	muscle
24	chr4:9664800-9675600	Weak transcription	Fetal Thymus	thymus
25	chr4:9672400-9672600	Enhancers	Brain Hippocampus Middle	brain
26	chr4:9672400-9672600	Enhancers	Fetal Stomach	stomach
27	chr4:9672400-9672600	Enhancers	Skeletal Muscle Male	skeletal muscle
28	chr4:9672400-9672800	Enhancers	Ovary	ovary
29	chr4:9672400-9673000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr4:9672400-9673000	Enhancers	Fetal Lung	lung
31	chr4:9672400-9673000	Enhancers	Left Ventricle	heart
32	chr4:9672400-9673000	Enhancers	Right Atrium	heart
33	chr4:9672400-9673200	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr4:9672400-9673200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr4:9672400-9687000	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chr4:9672600-9673000	Enhancers	Brain Inferior Temporal Lobe	brain
37	chr4:9672600-9673000	Enhancers	Fetal Muscle Trunk	muscle
38	chr4:9672600-9673000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
39	chr4:9672600-9673200	Enhancers	Fetal Muscle Leg	muscle
40	chr4:9673000-9692400	Weak transcription	Brain Inferior Temporal Lobe	brain
41	chr4:9673200-9692600	Weak transcription	Fetal Muscle Leg	muscle
42	chr4:9675600-9676000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr4:9675600-9676000	Enhancers	Fetal Thymus	thymus
44	chr4:9675600-9676200	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr4:9676600-9680000	Weak transcription	Brain Anterior Caudate	brain
46	chr4:9676600-9681200	Weak transcription	Fetal Stomach	stomach
47	chr4:9680200-9680800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr4:9681200-9682000	ZNF genes & repeats	Fetal Stomach	stomach
49	chr4:9681400-9681600	Weak transcription	Fetal Thymus	thymus
50	chr4:9681600-9682000	ZNF genes & repeats	Fetal Thymus	thymus

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