| Tag | Content |
|---|
EnhancerAtlas ID | HS012-11094 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr12:95492820-95494920 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr12:95492871-95492886 | TGAACTCCTGACCTT | - | 6.04 | | Nr2f6(var.2) | MA0728.1 | chr12:95494895-95494910 | GAGGTCAGGAGTTCA | + | 6.22 | | ZNF740 | MA0753.2 | chr12:95493831-95493844 | CCCCCCCCCCCCC | + | 6.03 | | ZNF740 | MA0753.2 | chr12:95493833-95493846 | CCCCCCCCCCCAC | + | 6.92 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr12 | 95493870 | 95493944 | | chr12 | 95494052 | 95494505 | | chr12 | 95494641 | 95494807 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I095097 | chr12 | 95491501 | 95493031 |
|
Enhancer Sequence | TTTTAATGTA AAATATTAAA CGGGGTTTCA CCATGTTGGC CAGGCTGGTC TTGAACTCCT 60
GACCTTAAGT GGTCCGCCTG CCTTGGCCTC TGAAAGTGTT GGGATTATAG GCGTGAGCCA 120
CTGCACCTGA CTTGACCCTT TTAATTTTTA ATCCACTGTG TCCCGATGCG CAGCACAATG 180
CCTGGCCCAA GGTAGAGGCT CCATATTCCT TACTGAACGA AGGGATGAAC TGCAGGTGGA 240
GGTAACACCT GTGGAAGGCA GATGGCTGTG GAGTTGTCTG GCATGCATGG AGTCACACGC 300
AGATCCGTGC TGATGGAGCA TGCAGTGTGT TGGTGGGAAG AGATGGAGAG ACTCCTTACC 360
CACTTTAATA TGGGATGCAG TACCTGCCTA ACTGGTTGGA GGAATCTGGA AGGAGAGCAT 420
GGCATACCGA TGACATTCAA TATGCCTTAG CTCTCTTTCC CTCATGCCAG CTTGATCCTC 480
CCTTGGAAAT TTATTTTTCC TTTATCAAGA ACTTTTCAGT TCAATGATTT CCCCTGCAGA 540
GCCCACATTC AGCCCATTAG TAATCCTATT GGGTTTTTTT CTGATTCATA CCATTGTTCA 600
TCACTTTAAC CCAAGACACA CCATCATCTG CTGGGCACTC ACTACCTGGC TGCCCAACTT 660
CTACTGTAGT CTCCTGATGG TCTGTCTTCT ACAAAGAAGC CGGTGTGATC TTTCACAAAC 720
ATAAATTAGA TATTATCACT TAGCTGAAAA CTCTTAAAAA TTCAATGACC TTACTATGGG 780
TGGCCCCTAA CTCTTGCCCC TAAACTGTAA CTCACATTTA ATCTCCCCTG GTACTAGGGG 840
AGTACTAGGC TCTCCCCGGA GTACTAGGCT CTACCTATAT TGGAATTCTT GCTGTTTCTT 900
TAACATACTA TACCCTTTCC TGCCTCCCTG GTATGTCTTT TGTTCCTGCT GTTCCTTCCA 960
TCTGGGATTT GCTTCTGGTC TCTGATGCTC CTCAGAGATA ACTTTTCTGA TCCCCCCCCC 1020
CCCCACCCCA TATAAGTTCT TGACCTCATC ACTTTCTATC TGCTCAGCCT ACTTTATTCT 1080
TCTTTATAAC ATTGAATACT CCAAATTATT TCTATGTGCA TAGATATAAA TAAACCTGAT 1140
TATTATGTAT CTCCCACTTT AGAATAAAAG CTTATCCTTA AGGACAGGGA TTGCACACCC 1200
CCAGCTCCTG GACAGGGTAG GTGATGCCCA GTAAACATTT GTTAATGGTT GATAGCAGAC 1260
AATCGCCTTC CCTCATAGCT CTCCATATGC CAGTCTCCAA ACAATGACTT TCTCTCATCA 1320
CTAAAGTTAG TTTGACTCAG CAATGATTGC TCTCAGTTAT CACTGCTTAT CACTAAGCCC 1380
CAGACTACTA ACAAAAGCAC AAACAGGACT GCCCAGACCA GCTGGCTGCT TGCTGCCGTG 1440
GCTACACTGT CTCGCCCACC ATGTCACTAC TGCTGCCATC CACAAGGCTC CCAACTCGGA 1500
GGCTAATCGC ACTGTTGGCT GTATCTGTTC CCACGACTTT CTAGGAGACT CCTGTGGCAT 1560
TCTTTTTTCC CACCCTTGGG ACTCTAAACC AGTGTGCACT ATGGAGCTTG GCAGAGCTGC 1620
AAAGCTGGCA CCAGAATTCA CCAAGAGCAA TGTGAAGTTG ACTGCCCTTG CAACAGACAG 1680
TGCTGAGGAC CATCTTGCCT GGAGCAAGGA TATCAATGCT TACAATAGTG ATGAGCGAAC 1740
AGAAAAATGC CCTTTTCCCA ACATTGATGG TAAGGATCAG GACCTTGCCG TCTTGTTGGG 1800
CATGCTGGAT CCTCCTGAGT TGGAAGAAAA GGGAATGGGT GTCAGAGCTT ATGGTGTTTA 1860
TTTTTGCTCC TGACAAGAAA CTGAAGCTGT CTACCCAGCT ACCACTGGCA GGAACTTGGA 1920
TGAGATTCAC GGGGTAGTTA TCTCTCTCCA GCTGACAGCG GAAGAGAGGT TGCCACCTTG 1980
ATTGATAAGA AGAATGGAAA TAGTTATGTT GCTGGGCATG GTGGCTCACG GCTGTAATCC 2040
CAGCACTTTG GGAGGCCAAG GTGAGTGGAT CACTTGAGGT CAGGAGTTCA AGACCAGCCT 2100
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