| Tag | Content |
|---|
EnhancerAtlas ID | HS101-11713 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr12:125624160-125626160 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr12:125625770-125625785 | TGGTCAGGCTGACCC | - | 6.04 | | IRF1 | MA0050.2 | chr12:125624835-125624856 | TCTTCCTTTCTCTTTCCCTTT | + | 7.26 | | RREB1 | MA0073.1 | chr12:125625224-125625244 | CCACAACACACCAACACTGC | + | 6.25 | | SPIC | MA0687.1 | chr12:125624511-125624525 | TACTTCCTCTTATG | - | 6.1 | | ZIC3 | MA0697.1 | chr12:125625025-125625040 | TCACAGCGGGAGGGC | - | 6 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr12 | 125624256 | 125624468 | | chr12 | 125624295 | 125626120 | | chr12 | 125625545 | 125625696 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH12I125138 | chr12 | 125623364 | 125624282 | | GH12I125139 | chr12 | 125624374 | 125626130 |
|
Enhancer Sequence | GCTGTGCAAA GCCCTTCCAC ACACCTGATC TCAGTTGCTC TCTGTGCAAA AGTCAGAGAG 60
GCTTTCCCTG CATTTCCTGT TTGAACAGTG TCCTGGCCTC CATCTTTAGC TTTGACAGTG 120
TTTACCATGG GGGTGCTGAG GGTGAGTTCT TGTGTATGTG CACATCTTTC TGGTGGAGTG 180
GAGGCCTCTT GAGGACAGGA ACCTTGTGGG TCTACCTCCT TTTCTTCGGA GCTCAGCTGA 240
CTGCCTGGCA AACAGCAGAT GCTTTTGGTG TCTGGTGAGT GAATGGGGGG TGGGGAGCTG 300
GTCCTGTGAC CCTGGTGAGG CGGGACAAAC TTGTCTTCCT CACACCCATC TTACTTCCTC 360
TTATGAGGAA ACCCAGAGAG ATGAGGGGTC TTGCCCAAGG AAGGGGTGTC CATAGTCAGC 420
TCTGCCTTCT GCTCACCCAG AATAAAGACC TGGGGACCCC GCGAGGGTCA TGGCCAAGTG 480
GAATGGACTC CTGGCATTTG AGGGCTTCCC GACTGCAGCC CTCAGGCAGC CATGGCTGTC 540
CCAAGTCCAG CGGGCCTTTG CTCGGGTCAT GGCTGGGATG TCTGGCCCTT CCTGACAGGA 600
GGCTGCTGGG CTCCTGTCTA CTTGGGGACG CCTCATGCAG GAGCTGGTGT GGGGGTGGGC 660
AGGGGGGCGG TGGCTTCTTC CTTTCTCTTT CCCTTTCCTC TACCTTTTCC CCTCTCCCCA 720
GAGGAAATGG TAGCAGGATT TCTTTTAAGA GGATGCTGCT GTATTTTGCC AGCGGGTGGA 780
AGGTGGCGGT ATTAGCTCCC GTGAGCTGCA CGTGGACCCC TGTGTGAAGC GTAGCAGGGC 840
ACAGAGCAGG CGAGACGTTT GCATCTCACA GCGGGAGGGC CGGCGACATC ACATGAAGTG 900
ACAGGCAGGC CCTTGGAAGC CGGTGCTTAG ATCCTTAATT AGTTCACACG TCGACTGAAT 960
TTTCAAGTGA ATGAATTTTA ATTACATCTC AGGTTAAAAA AAAAAAAAGG CGCCAGTGAT 1020
CGAGGACTCG TCACTGGGCT CTGTTGCTCC TGAAGTTTCC TAGCCCACAA CACACCAACA 1080
CTGCCAAGGG CTCTTCTGGA TTCAAGGTGA AACACATGTG CCATAAATCT TGGAGCTCTG 1140
AATGTTTGGA AAGGGCCCGA CTGTGAGAAG AAGTAACACA CCGTCCCGTG CAGATGGCTG 1200
GCTCTGAGGA GGAGTTCATG GGAGCTTGGG GACACTCTTG CCTCTAGTTC TAGGAAGCTG 1260
GGCCACTTCT GAAGTAATGG CAATATCAAT AAAGTAATGG TCTTTATCAT AGAATAACGT 1320
GATAAAATAT ATAGAGAAGT AAAAAAGTAT AAATAAAAGT AAAATCATCA TAAAACATAG 1380
TAGCTAGGCA CTTCTGAAGC TGTGTGTGCA CTGATTCATT CACCCAGTGA CTCACAGCCT 1440
TATAGCCTAG GTGCTGGCAC CCCTACTTTC ATTCGAGGAA GTGAACTCAG GTTCAGGAAT 1500
TTACCCAGCA TCCCCCAGAT GGGGTGGCAG GAGCCACATC TTCCCTGAAA ACTTTCTTGC 1560
CCAGGGTGTC TGCTGGGATT TAGGAATGGT CTATGCCTGC ATTTTTATCC TGGTCAGGCT 1620
GACCCTGAAC CCTGAGAGAT ACTCTTTTTT ATATTCCCAT CTGGAATATG CACTGCCGGG 1680
GTCAGTGGGG TGTCTGGAGG GCCCTCTCGA GGCCAGCTTG GATGTGACAC GTGTCGTGGG 1740
TCCCAACGGG GCCCAGTAGA GTGTGCAGCG TTAGAAAAAT GAACATGCTC GGCTGGGCGC 1800
GGTGGCTCAC GCCTGTGATC CTAGCACTTT GGGAGGCCAA GATGGGTGGA TCATGAGGTC 1860
AGGAGATCAA GACCATCCTG GCTAACATGA GACCATCCTG GTGAAACCCC ATCTCTACTA 1920
AAAATACAAA AAATTAGCTG GGCGTGGTGG CAGGTGCCTA TGGTCCCAGC TACTCAGGAG 1980
GCTGAGGTAG GAGAATGGTG 2000
|
