| Tag | Content |
|---|
EnhancerAtlas ID | HS091-09938 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr12:52549880-52551920 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CDX2 | MA0465.1 | chr12:52551507-52551518 | TTTTATTGCTT | - | 6.32 | | CTCF | MA0139.1 | chr12:52550727-52550746 | TGGTCAGCAGGGGGCGCTC | + | 6.96 | | MEF2A | MA0052.3 | chr12:52550558-52550570 | TTTATTTTTAGA | - | 6.07 | | MEF2C | MA0497.1 | chr12:52550557-52550572 | TTTTATTTTTAGATA | - | 6.26 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_23126 | chr12:52548724-52550474 | Colon_Crypt_1 | | SE_23778 | chr12:52549428-52550433 | Colon_Crypt_2 | | SE_26568 | chr12:52536245-52551492 | Esophagus | | SE_34629 | chr12:52536709-52551617 | HeLa | | SE_35885 | chr12:52537041-52552074 | HMEC | | SE_64292 | chr12:52537455-52551439 | NHEK |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I052143 | chr12 | 52536922 | 52551852 |
|
Enhancer Sequence | TGATCAAGGG CTATGTGTAT GCACATGTGC GGATGTGTGC TTTGATGGTG GGCCTCAGTC 60
TGCCTGCGCC TGTTGAGGAC ACCTGCATGT AGGCGTGGAT GTCTCCGCCC AGGGATGGAG 120
GTGTGCACAC AGATGTCCAT TTGCACTTAT GTTTGCACAA TGCACGTATG TTGGGTACAC 180
ATGTATGTGT TGTATGTGTG CACATGTGAA CATATGCATA AGAACATATG CTTGTGCACA 240
GTGTGCCTGC ATTTGTGAGT AGGTGTGTGC ATAGGCTGTG CATATGTGTG TTCATATCTG 300
CAGATAGCCA TGTCCCCAGG TATATGTGGT CATCTCCAAA GGCTGACCTC ACTCCAGTTC 360
ACTCAGCCTG TGTCCCCTTC TCAGGCTCCT GACTCACCAC ATGTGTGGAA TCTATTTGCA 420
TGTCAGTCCC ACTGAGTCAG TGTCACAGCA GGATGTGTGA TGGCCTTGCT GGTGGTACAG 480
GGACTTCGAA GGAGGGGCGC TTGGGGAGAG GTAGGATTGG CAGGGATGAG TGTTGAATAG 540
GAAGGTGGCG GATGGGATGA AAGAGATTAA GGCCAGGTGT GGAGGCGGGC CTAGGTGTTT 600
TTCAGCCCCC AGTCAGGGGT AGAGGCCTCA AGGAGGCTAA TCCTGCCCCC TGTACTTACC 660
TCTTTCTTAT TTTTTATTTT TATTTTTAGA TAGAGATGGG GTCTCACTAT ATTGCCCAGG 720
CTTGTCTCGA ACCCCTGAGC TCAAGCGATC CTCTCACCTC GCCCCAGGAA CAGCTCTTTG 780
CACTGTCCCA GACCCCAGGC CATAGGTATC TGGTTCCCCA TTGGGCGTGG AGGTGCAGAT 840
GAGGCAGTGG TCAGCAGGGG GCGCTCAGAG CCTGCAGATG GTGGGGAGCC ATGGAACAAG 900
CAGGTGGGAA TGGGAGTGGG GAGGGTAGGG CTGAACCACG GGCACAGACC CACCTGCGGG 960
GAAAGGGTGG AGGAACATGA ACTTTGCAAC ATGAGGGGCA GACTCCCAGA GGGCCAGATA 1020
TACACATCCT CCCCAGAGGG ACAGGCCCTC TCCAACAGAC TCACAGACCC TCAGAAGGAC 1080
AGACACAGGG ACAATCCCTC ACCCTCTGAG AACATTCCGG GCCCAATGAG CCGGAGGGAG 1140
GTGAGAGTGA CCACACTGGC CTGCATGTCC CTCTGGAGGC AGGGGGTGTT GGCTCTTGGT 1200
GACAGTGAGG AGGGGAAGGA AGGCAAGGGC TCTAGAGTCA GGCACGCTCA AGGTCTGACT 1260
TCAGCGTTGC CTCTGGGTGA CCTGAGCTCT CCTGAATGGG GCAATGTCTT CCAGGTGTCC 1320
AGCTCAGGCC TGGACACGCA ACGTCACCCT GGAGGTTATG AGAGGTTGCC AGAGCCTCCG 1380
TCATTGGTAT GTCTGCACAT TTCTCCAAGC ATCTACTAAG TGCCAGGTCC ACTGCAAGGC 1440
GCTGGGGATA TGGTAATGAT CAAGTCACAC TCAGTGGCTC CTGCCACTGC TAGGGAGCTA 1500
ACATTCTAAC GGGGGGAGTA TCTTAGGATA CTTGGGATAC AAAATGATCA CTATTCCCCC 1560
CATTTGATTA TTTGAAGTGG AAATTATGGG ACAAAAGGCA GAGACTGGCA GGGAAGGCCC 1620
TTTCCTCTTT TATTGCTTAT CAAATGCAGG CTGAGAAAAG TCCAGATATT ATGGTACTGC 1680
TGTGGTCCCC TGCCTCTTAC TGCAGAGGTC AGATCCAAAC CCTCCATCTC ATTCAGTCAA 1740
AGCTGAGGTT CAACAGTGGC CCCTGAGGCC TAGTGTAGGC TGAACCCCCC GCCTCTCCCC 1800
TCATCCCTCC TCGCAAGTCC TCAAACATGA TAGGCAGGTT CTGCCTCCGG GCCTTTGCCC 1860
TTGCTGTTCT GCCTCTGGGC CTCTGGCCTT GCTATTCTCT CTTCCTGGAA TGGTCTTCCC 1920
CAGGCTTCTG CGTGGCTTGT TTCTTCATCT CTTGTTTTTT TTTTTTTTGA GATGGAGTCT 1980
CACTCTGTCA CCCAGGGTGG AGTGCAGTGG TTCAATCTCA GCTCATTGTA ACCTCTATCT 2040
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