| Tag | Content |
|---|
EnhancerAtlas ID | HS024-16606 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr9:140559230-140562980 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GLI2 | MA0734.2 | chr9:140559447-140559462 | GGACCACCCACTTTG | + | 6.63 | | LMX1B | MA0703.2 | chr9:140561342-140561353 | GTTTTAATTAA | + | 6.14 | | Lhx3 | MA0135.1 | chr9:140561346-140561359 | TAATTAATTAATT | + | 6.78 | | Lhx3 | MA0135.1 | chr9:140561350-140561363 | TAATTAATTAATT | + | 6.78 | | Lhx3 | MA0135.1 | chr9:140561347-140561360 | AATTAATTAATTA | - | 6.78 | | POU6F1 | MA0628.1 | chr9:140561348-140561358 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr9:140561352-140561362 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr9:140561348-140561358 | ATTAATTAAT | - | 6.02 | | POU6F1 | MA0628.1 | chr9:140561352-140561362 | ATTAATTAAT | - | 6.02 | | RARA(var.2) | MA0730.1 | chr9:140561844-140561861 | AGGCCATGTGGAGGTCA | + | 6.38 | | RREB1 | MA0073.1 | chr9:140562773-140562793 | CCACCCACCACTCACCCACC | + | 6.02 | | RREB1 | MA0073.1 | chr9:140562777-140562797 | CCACCACTCACCCACCCACC | + | 7.06 | | ZNF263 | MA0528.1 | chr9:140561887-140561908 | TACTCCTCCTCCTCCTCCCCG | - | 6.21 | | ZNF263 | MA0528.1 | chr9:140562728-140562749 | TTTTCTTCCTCTTCCTCCATT | - | 6.39 | | ZNF263 | MA0528.1 | chr9:140561881-140561902 | TCACTCTACTCCTCCTCCTCC | - | 6.55 | | ZNF263 | MA0528.1 | chr9:140561878-140561899 | GCCTCACTCTACTCCTCCTCC | - | 6.56 | | ZNF263 | MA0528.1 | chr9:140561884-140561905 | CTCTACTCCTCCTCCTCCTCC | - | 8.31 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_11232 | chr9:140561146-140563373 | CD20 | | SE_32833 | chr9:140558964-140562778 | H1 | | SE_41929 | chr9:140559711-140561304 | LNCaP | | SE_58494 | chr9:140551343-140601094 | Ly1 | | SE_62965 | chr9:140561512-140658488 | Tonsil | | SE_68889 | chr9:140558888-140562343 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr9 | 140562371 | 140562671 | | chr9 | 140559752 | 140562041 | | chr9 | 140561000 | 140562084 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I137664 | chr9 | 140558495 | 140562715 |
|
Enhancer Sequence | GTTTGTAAAT GACCACGCTC TGTTGCCTTA AGATGGATCT GTTGACATTG TGTTTTCTAC 60
ATTTGAACTT GGAGTCCCAT GTCTGGGTTG TTTGCTCTTG GCTGGGCGGA ACCTGTGTAC 120
TTAAAGAGGA ATCACTTGCA TTGCTTTTCG GACATGGTGT TTTGTTGGTG CGTCTCCTCC 180
CTGGCTGGTA AGCACAGCTT GCGGGCCTGG CTCTGTTGGA CCACCCACTT TGCAACTCTT 240
GGGCAGTCAA CACTGATACT GTACTAGAAA GCGTGGGGGA GTTATAGAAT AGCATTTATA 300
GAGAAGGATT GGTGTTATTT ACTTTCATGT GACCTTAAAA ATAGAAAATA ATATTTGTGC 360
TTTTATTTTG CAGTTTGCCT GGAACCTGAA TACACTATTT TAAAAAATAT TCCCTATTTT 420
TATAGAAAAA GGACTTCAAA TATTTATTGT TTTGTATTAA GAGCTACAAA CAACTTGGTC 480
TTGATTGGAG AGCTGGCATA GGTGTATAAG GGCCTCTCCC TGTAAGAAAT TTGGAGCTGG 540
GGTGGGCATA GGAGGTGATG TTTAGGAGCA GCCTGAGTGT GGGGAGACTG CTGTGCTCGA 600
ACCTGCGTCG TGCAGGTGCG TCCTGGAGCT ACTCCTTGTG GCAGAAGCAT TGCCCTGAGA 660
CCCAGCCCTG GTATGCTTGG CACTGGGACA GGAGCTCCGG TGGGAGGTGC GCATTGCGAG 720
CTGGTGTTTT CTGTTTGCTT TCCTACCCAC TGTCATGTTG TGGGCTCTTG GCCCCAGAGG 780
TAAAATGTCT CTGTGAGTTG AGTTCCTTGT GAGAGGGCTG GTCCCCAGAT TCCATGTCTA 840
GGTTTTTGTT AGTATTTTTT CAACAGAGCT AATCCTGAGA GGCCCTACGA GCAGTGATTG 900
CTTTGTGGGA TGAGCTGTGT TGATGGTTTC TGTGGAGGGA CCCTTCACGT TTTAGGGTGA 960
AAACAATAAA TGTCTCGTTA AATGGTTTCC ATCTGAGAAC ACTGATTGTT TTAAAATGGT 1020
TGTGAATGCG AGGGTTTAAG CAGCTTCCGA GGAGGCCTGG AGGTGCCTGG GCGGCCGCGT 1080
GCAGCTCTGG AATCCTGCCG CTGGGGCAGC CTCCATTTCG TGAGATGGCT CTGGAGCATG 1140
CCCAGTGCGT GGAGCTTTCA GAGGGAGCCG CCGAGCTGGG CTACTGTGAT TTCTCTGCAG 1200
TTGGCCGCAG TCAACAATTG CACTAAGACA GGAGGAAAAA AGTGATGGGG TACAAGCAAG 1260
AAACGTGGTA TTTGGTACTT TTTTTCTTTT GCTTAATCCC TCTTTCTTTT ACATTGGTGC 1320
TTCTAGGCTG GGGCCAGGGC CTGCAGAGCA GGGACGCTTG CTGTGATGGT GGGGACACCT 1380
CCTTGTCCTC CATGCCGCTT GCCTGCCAAA ATAACCCTGT TTTGCTCTCT GGTCACCCAC 1440
CATGTGCACT TTCTTGGGAG TGGGATGGGA GGTCCCCTCC AACTGAGGGT ACTGAGAACA 1500
GCTCAGGCCC GTTCCACATT TGCTGGTAGC AGGAGGAACT CTGACCTTTT TCAGTTATGC 1560
TGATGATAAA CCAGGACTTT TTCCCTTGTT TGAACATTTA TAAAGAGCGT GCTTGAACTT 1620
TTTTGCTGAC TAGCAGTGTT TTCCTGTTTT ATTCTCCTAC CTGCCCCCAT GGCAGCCTCA 1680
GTGGTGGAGG GAGTGAGGCT GGGAAGGGAT GACACTGCCA GGTGAGCAGG AACCAGGGAC 1740
CCTGGGACCA GAGGCCAGGC TGTGCAGGGC AAGGGCTGGC CGTGCCACGG TGCAGCTGGC 1800
TCTTTGCCAT GCAGGCTGCA GAAAAGGAAA TCTGTCCGCC TTGGCTGTGA GGATGGCATT 1860
GACCACTCAT CAGGAGAGCT GGGAACAGAG CCTCCCCCTC GGAGCCTGTG TAGTCCCCGT 1920
CCACACGTGT GGGTTGTGTG ATGATCCTGT CTGCGTGTTC ATTGGGAGAC TCCATTTTCC 1980
GTGGAATGGT GAGGAGGGTA GAGAGGCAGC AGAGTCTCCA CTTGGATTTT CTAAGCAATT 2040
CCACAGAAAA TAAGACGTTG CTCAAGCAAG TGCTGGGCAC ATCTTAGGGA GAGACCTAGT 2100
GAGGAGGGCT GTGTTTTAAT TAATTAATTA ATTGTAAATA ACAGGATTAG AGCAGATTGG 2160
TTCATAGCTG CCTGTTCTAG AACCGTATTC TTCGAACAAA AGGGTGGGGG ATGGTAGGCT 2220
TCTCTCCTAG CTCTGAGGAA ACTCCAGCTC AGCGCACAGC ATGAGGAGGA CGAGGGAACA 2280
ATAGGGCGTT CCTTTGTGCC TGCCCTTGAA ACGCGGTGGA GGCCACTCAG TGAGCCCGGG 2340
CAGTGCCATC GCTCACGTGT CCCCAGCAGC AGTGGCGTCT GTGGGGATGC TGTGCACTGG 2400
AAATTGGCAC TGTTTTGGGT AGTGGTTCTG AGAGGAACTG TTTAACCAGG TATGCAAATG 2460
TGCTGATGCA GGAATGTTTT TGAACACCTG TGATGTAAAT TTTAACGGTG GTTAATGTTA 2520
GCAGCTCCAC CTGGGTTAGC TCAACCCTTA GAGATTATTT GTTCTCATCT CTTTGGAGTT 2580
GAAAATGTTG TACTTTTCTA GGAGCCATTT CCCCAGGCCA TGTGGAGGTC AGGTATCTGC 2640
TGGTTCTGGC CTCACTCTAC TCCTCCTCCT CCTCCCCGCT CTGTGGAGAG GGTGGCTTGA 2700
AGGAGACGGG CAGCAGGTGT GTGACTGCAG TCCTGGGGCA CGGGCAGAGG CTGGCATGTG 2760
GGGAAAGCAG GACCCGGGAG GCTGTAGCTT AAGTAGACAT TTGTTTTTTA TTTGAAGAGA 2820
ATTTTAGAGA TGGGGTGGTG GTGGATTTTA GCATTAGAGA TTTCTGGCTT CTGCTTGAAG 2880
CACTGTGAAT AGGGGACAAA AAAATAACCA AGAGGAAAAG TTCATGTAAA GTAGAAGTTT 2940
TGGTGTGTTT TCTTGAAAGG AAATTGTCTA CAGTGAAAGC GTTGTATTTT TAGAGAACTC 3000
GGGGAGGAAA ACGCTGTTGT GCTGCTTATC ACACGGGTCT GGCCTTTTTG ACATCTGAAA 3060
TCTTATAGGA ATTTGTCTTT TTGAGAGTGT ATGCTGCTTA TTTGGTTTCG TGGAATCCAG 3120
AAAAGAGCCT ATCCAAATTA TCTTTACCTT CAGGGTAAAT TACCTTTTAG AATTGTGGCA 3180
GATGGCACAT AGGACCTCTC AGAGGGACTG CACCTTGTAC AAGAAGAAAA GTGAGAGGGT 3240
GTTGCAAAGG AGAGCTTCCA CCTCCTTTAT AGACTTTTGC AGAACAGCTT TCTTCCTTTC 3300
GACCTTGGAG AAGAGGCAGG ACCAGTGGGG AGGCAGACAA GTAGGTGAAG GAAGACAAAA 3360
GGAAGAAGGG ACGCACTGAT CGAGAAGACA AGGAGTGCTG ATGGCTTTGG GCGCCAGCTG 3420
TCTACTCCAG AGAGTCTAAC TGACCTGGGA CTTGCAGGAT CCTGCTAGAA GAAAAATCCT 3480
TGCTTCCTTC TCCTCCTGTT TTCTTCCTCT TCCTCCATTC TCCTTCCTCT CCCTTCTATT 3540
CACCCACCCA CCACTCACCC ACCCACCACC TGGCACATAC ACCCACCCAC TCATCCATCC 3600
ATCCATCTAC TGTCTACTAT CCACCTCACC ACCCACCCAT CCATTTATTT ACCCACCTAC 3660
TCATCCATTC ACCTGTCCAC ATCCATCTAT TCACCAACCA TCACATATTA ATGACTTACT 3720
ATATACCAGA ACTACTAGTA CTGAAACTTG 3750
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