| Tag | Content |
|---|
EnhancerAtlas ID | HS101-11607 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr12:123130610-123132780 |
Target genes | | Number: 15 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF1A | MA0046.2 | chr12:123130734-123130749 | AATTAAAAATTAACA | + | 6.4 | | IRF1 | MA0050.2 | chr12:123131786-123131807 | TCTATGTTTCATTTTTACTTC | + | 6.03 | | POU4F2 | MA0683.1 | chr12:123131256-123131272 | CTCATTTAATATGAAT | - | 6.13 | | SRF | MA0083.3 | chr12:123132485-123132501 | TTTCCAAATAAGGTCA | + | 6.01 | | Six3 | MA0631.1 | chr12:123132763-123132780 | TATAATGATACCCCATC | - | 6.47 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr12 | 123131126 | 123131793 | | chr12 | 123131021 | 123132400 | | chr12 | 123132400 | 123132436 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I122646 | chr12 | 123130749 | 123132415 |
|
Enhancer Sequence | ATAAATGTTT AAGGTGATGG ACACCCCATT CACCCTGATG AGATTATTAC GCATGGCATG 60
CCTGTGTCAA AATATCTCAT GTATCCCATA AATATATACA CCTACTATGT ACCTAAAAGT 120
TAAAAATTAA AAATTAACAA CAAAAGGCTG GCACGGTGGC TCACAGCTAT AATCCCAGCA 180
CTTTGGGAGG CTGAGGCAGG TGGATCACTT CAGGTCAGGA GTTTGAGACC AGCCTGGCCA 240
ACATGGTGAA ACCCCATCTG TACTAAAAAT ACAAAAATTA GCTGGGCGTG GTGGCGCGTG 300
CCTGTAATCC CAGCTACTGG GGAGGCTGAG GCAGGAGAAT TGTTTGAACC TGGGAGGCGG 360
AGATTGCAGT GAGCCAAGAT TGCACCATTG CACTCCAACC TGGGCAACAG AGCAAGACTG 420
TCTCAAAAAT AAATAAATAA ACAAAAATAC AAATTAACAA CAAAAAAAAA GACTCTCTGG 480
TCAGACTTTT TCACTCCCTG TCTTGTATCC GGGATACAAT TCTCTGCACG TTTCATGCTG 540
TTTCAAGTCT TTGCTCCCCT TCCCTCTTTG CCTAACTAAC TCCCACTCCC TCTTTATGAC 600
ATGATAGTTA CTTAATATCC AAGTTCCTGG AATTGCTTGA AACTGTCTCA TTTAATATGA 660
ATATACATAT ATGTAGGAAG CATTAGGACA TTCCTTATAT TCAAAGAGCT AATGTAATGA 720
ATCAGGAGGA AATGTTATTA CCTCAAAACC AAATGATTGT CAACTCATGT TTTCTGATGT 780
TATTTAGGTA GGCTTGGTAA CTTGGTTATA TCTTAAAAGG GTACATTACT CATAACCCAC 840
ATTATATTTC ATACCTCAAA AGAAGAAGTG GTAATTTACA AAACTTCATC CCTCCCCCTT 900
CCCCGTGGTG CCATGTGCTT GGCAGTTGGT GTTTTGGTCA GATCTAAGAA AAGTTTCATC 960
ATCAAGCAGT ATGAACACAT GTGCCGGTGA ATCTCTGTCT CCCTTTTTTT TAATGACTCA 1020
TAACCGGCCA CAGGGTACCA CATTTAGGGT GACAGCTCTA CCATTCACGA GTTTGGCATG 1080
TAAACACAAG ATCCCCACGT GCAGATCTAT TGATGGGTGG TCTTTTCTCA GAAAGGTACA 1140
TTCTTCTGGC TCGGTCTAGA TTACCGGTGG GATTTTTCTA TGTTTCATTT TTACTTCTGT 1200
GCTTTCGGAA GGACAAAGGG AAGCTGACAG CGAGGGTGAA ATGAAAACGT AAGTGATAAG 1260
GGTTGTAAGA AACAATGAAA AAGATGTTTT TTGTTGGCTT TTTTTTTTTT TTGGAGATGG 1320
AGTCTCACTC TGTCCCCCAG GCTGGAGTGC AATGGCGTGA TCTTGGCTCA CTGCAACCTC 1380
CACCTCCCGG GTTCAAGCGA TTCTCCTGCC TCAGCCTCCC AAGTAGCTGG AATTACAGGC 1440
ATGTGCCACC ACACACGGCT AATTTTTAGT AGAGACAGGG TTTCGCCATG TTGGCCAGGC 1500
TGTTCTTTAA CTCCTGACCT CAAGTGATCC ACCTGCTCTT GGCCTCCCAA AGTGCTGGGA 1560
TTACAGGTGT CAGCCACCAT GCCTCGCCAA AACAACAGAA GTTTATTTTC TCATAGTTCT 1620
GGAGGCCAGA AGTCAGCAAT CAAGCTGCCA GCAGATCCAC ACTCTCTCCA AAGTCTCTAG 1680
GGGAGGATCC TTCTCTGTCT TTTCCAGGCA TCCCCTGGCT CATGGCCACG TCACTCCAAT 1740
CACTGCTTCT GTCTTCATGT GGACTTCTTC TCTGTCTGGC CTCTTCTGTC TCTTCTAAGG 1800
ACACTGTCAT TGCCCACCCT AATCCTATAT GATCTCATCT TGATCCTTAT CTTAATTCCA 1860
TCTGCAAAGA CCCCATTTCC AAATAAGGTC ACCTTCTGAG GTTCCCGGAA GACATGAATT 1920
TAGCAGAGGG CACTCTTCAA CCTTCAACCT ACTACAACCT CCTTTCTCAA TTTCCACTGC 1980
TTCTGCCTTT GGGTGAAGTA TAGAATCCTT TAAATAACAG TGTGCTTTCT GTGTAGTTAT 2040
TGATTAGAAA TAATCTGGCC AGACACAGTC GCCCACGCCT GTAATCCCAG CACTTTGGGA 2100
AGCCAAGGTG GGAAGATTAT GCGAGCCCAG GAGTTTAAGA CCAGCCTGGG CAATATAATG 2160
ATACCCCATC 2170
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