| Tag | Content |
|---|
EnhancerAtlas ID | HS105-41641 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr2:10080740-10082630 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr2:10082188-10082208 | CCCCCACCCCCCCCACCCCC | + | 6.38 | | RREB1 | MA0073.1 | chr2:10082189-10082209 | CCCCACCCCCCCCACCCCCA | + | 6.46 | | RREB1 | MA0073.1 | chr2:10082184-10082204 | CCACCCCCCACCCCCCCCAC | + | 6.61 | | RREB1 | MA0073.1 | chr2:10082187-10082207 | CCCCCCACCCCCCCCACCCC | + | 6.8 | | ZNF263 | MA0528.1 | chr2:10082399-10082420 | CCTTCTCTCTCTTCTTCCTTT | - | 6.18 | | ZNF263 | MA0528.1 | chr2:10082187-10082208 | CCCCCCACCCCCCCCACCCCC | - | 6.58 | | ZNF740 | MA0753.2 | chr2:10082191-10082204 | CCACCCCCCCCAC | + | 7.52 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_27370 | chr2:10080531-10082772 | Esophagus |
|
| | 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 |
| GH02I009940 | chr2 | 10080836 | 10082163 |
|
Enhancer Sequence | TTTACCTTTC TCTCCTTAGC AACTGACACC AGAATAAAAA TCTCCCTGGA AAGGCTCCTC 60
TGGTCCCAAG CGGTCACCTG CTCCGGCCCC AGAGCCCCCG GGGGTAGGGA GGTGGGCTCT 120
GTGCCTCTTC CCCCTCCACT GTCCATCCTG CCACAGCAGT TCACAGGGTC AGCTCTTCCG 180
CTCTAAAACT GGTTTTGTTT TTTGTTGTTT TGTTTTGTTG CAATTGCCCC GTGCTAAGTG 240
CAGCCCACGG CCCTCATGTG GAATGGGAAT CAGGTAGTAA AGTCAGTAAT GTTGGTTTCG 300
CCTGCCCCTC CTCACCACAG CCCAAGGGTC AGAGCTGTGG AATGGCCTCT TAGAACCCAG 360
CTCTATCACG CCCTCCCATC TCCCACTGCT GCCCAGGAAG GGTAGGGACC CAGGATCCTG 420
CACCCCTCAG ATCATTCTGT CTCCACTCAC TTTCTTCAAT TCCTCCGCAC CTACAGCACA 480
GCCTATTTTT GACATTATCA TAGCCTGCTT ATGTGTGTCC TGGTTTACTA ACTAGACAGG 540
CTTTCGTGAG ACATGGCTCC TACAGAACCC TAAATCCAAC AGATGTTCAG TAAATGCTTT 600
GATGAAAGTA GTGATGAGAA AGGGGAAAAT TACAAAAAGC TTCCCACTTT CTGATCAGCT 660
ACTGCTGTAC TGTTTTCACT ATTCAGTGAT TTCACCATTC TGTGAATGGG CTCAGTTGTC 720
TGCCTACAAA TGTTGGTTTT GAGTCAAACT GAAGTTATTT GAAGACAGAA GGAGGAAATG 780
GGCCTAAGTT TCGCCCCTGG CATTCCTGTG GCCATATCAA ATATTTATAT AGTGCTTAGA 840
GTGGGCCAGG CATTTCACAT GTATGGACTC TTTTATCCAT ACTTTTAGCA GCCCTACGGT 900
CCTGTAATAT TGTACAAAGG ACGACCTGGA GACACACAGA GGTTCAATTA CATCCCCAGG 960
GCCGTGTTGG TAAGCATGGA GCCGGGCTCT GATTCCAGGC TGTTGGCTGA AGTCTGTGGG 1020
CTTGGCCAGC CTACCGTGCT GCCTCACCAA GACTCAACCC CTGGTGATGT CAGTTTGGAA 1080
TCTAAGGAGC CCAAAAGCTG CTCAGAAGAA AACTAGATCA TTTACAACTA GCATATATCC 1140
TCACCACCCC TCCTCCATGC CTCCACCCCA AACCTGTTCT TCCTCTGCCT TCCCTGACTC 1200
AGTGACAGCC CCGTCCACCT AATTGCGCCA AGTCATAAAT CTCCAGCCCC TCCCTCCCTG 1260
TCACCTCCAA ATCTCATCCT CACTTCGCTG ACTTTCTACC ACCAAGCACC TCTGGACTCC 1320
GCCCTCCTTC GACAGTCACT GCCCAGCTCT GGCGCTCCTC GTGTTCTCCC AGGAGCTGCA 1380
AAGCTCTCTC CCCTCCAACA CACATTGCCC CTCTGCCAGT TATTTTCCCA AATCGGGTCT 1440
AAACCCACCC CCCACCCCCC CCACCCCCAC AATATGCAGC ATCCTCCCAA GGCTCCTGTT 1500
GCCTAGAGGC AAGAGACAGT GTGTTCTGGT TGAGCTATCA GAGTGTGGCC CCAACACTTT 1560
TCCCATCCCC CGCCCTGCCT TGCGCCCTCG ATCTCAGGCA AGCCATGGCC TCTCACACCC 1620
TGAGGCCTTT GCCTGTGTTG TATGCTCTAT CAGAAATGTC CTTCTCTCTC TTCTTCCTTT 1680
AGGACTCTTG CTCTATGCCA TCTCCCTTCA ACCCTCCCTA CCTCAGCTCC CCAAGCAGAG 1740
TTCATGGTTT CCGAGCACAG AGCTCAGACC TCCGTAAGGG CATGCACCGT CTGTGCCACA 1800
TGCCTGGGTC TCTAGATGGA GCCTCCTTGT GCTGGCCCAT GAGCTTTCTG TGCACACAGA 1860
TGCCAGTACC CACAGGGCAG GTAGGCACTA 1890
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