| Tag | Content |
|---|
EnhancerAtlas ID | HS110-04014 |
Organism | Homo sapiens |
Tissue/cell | KATO3 |
Coordinate | chr6:2542410-2543950 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MNX1 | MA0707.1 | chr6:2542635-2542645 | GGTAATTAAA | + | 6.02 | | PHOX2A | MA0713.1 | chr6:2542637-2542648 | TAATTAAATTA | - | 6.62 | | PROP1 | MA0715.1 | chr6:2542637-2542648 | TAATTAAATTA | + | 6.32 | | PROP1 | MA0715.1 | chr6:2542637-2542648 | TAATTAAATTA | - | 6.62 | | Phox2b | MA0681.1 | chr6:2542637-2542648 | TAATTAAATTA | - | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr6 | 2543800 | 2543859 | | chr6 | 2542443 | 2543800 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I002541 | chr6 | 2542133 | 2543933 |
|
Enhancer Sequence | CTGTCCTGTG TGTTTCTCGA GTTGAATGTG TCTCTCGGCT ATCCGGGTGG GTAGGGGCAT 60
AAGCCAGTGA CATACGATGA ACCTACTTGA CCTTCATGCT AAGATCCCTC TGACACTAGT 120
TGAACAGTTA AACTTGCTGA ACTGGTTCTC CCCAAATTCC TATGTTAAAG TCCTAAACCC 180
CAGTACTTAA GAACGTGGCT GTATTTGGAA ATGGGTTTTT TAAGAGGTAA TTAAATTAAA 240
ACAAGGTCAT TAGGGTGGGT CCTAACCCAA TCTGACTGGT GCCCTTATCA GAAGAGGACA 300
TGAGGACGCA GACATGCAGA GAGGGAAGAC CATGTGGGGA CACAGGGAGA AGCCAACCCT 360
CCACCAGCCC AGGAGAGAGG CCTCAGGGGA AACCAACCCT GACGACCCCT TGATCTCAGA 420
CTCACAGCCC CAAAGACTGT GAGGAGACCA GTCTCTGTTG TTCAAGTCTC TCAGTCTGTG 480
GTGCTTGTTA CACTTTCCCA GCTGCCATAC TCTCTCCCAC CTGGATCCCT GCAACAGCAT 540
ACACCTGGTG TCTCAGTGCT CACTTTGCTG CTGAGAAATA AAGATAAAAT CCTAAGCCCC 600
TCAACCAACT GAGCAGACAC TCTCTTGGCC AGGGGAACCC TAGAGAAACT GTAAAAACTG 660
AGTTCATGGC CATGATGGAT AGAAGGTCAG ACACGCCTTG CTATACCCGC TCCCTTGCTA 720
ACCGCCACTA GGTTTTCTTC CTCAATGGTT AAACAGAAAC CAGCTGTTTT GAAAGACTAG 780
CTCCATTGCT GATTTTGAAG AATCTCCTGA CTTCTGCCCC TCCCTTTTGT GGTTTCAACA 840
CAACTGCGTT CCTTCCTGAT AAGAAACCAC CAACCACAGA GTGGTTCTGC TGAGTCTATG 900
GAGATTGCAT ACTAAGGGTT TTCCTGTCCT CCACTTCACC TTCTGATCTC AGAGGGCCAA 960
ACACTCCACT CTCAGGTTAT GCTAGCACTG TCATTTTTTT GTACATGCCA CCCATGAAGA 1020
GGCATGAAGC TCAATTGCAC ATGTGCACGT TTCTCCATTC GTGCCTCCTT CTGTAGCTTA 1080
CTGAATATGT GCATTTGGTC ACCTGGTTCA GCATAAATCC CTTTTACATT CTTCCCACCT 1140
TCTAAGTGTC TGTTTCTAGC TTCTGGCCAG AGGCTACGCT TCCCAACCTG TCAGAATGGC 1200
TACCCTGCAG GATGCAACCC TGTATGAGAA ATCTCTCCTT TCCAAAAATA TGAACCTCAT 1260
TATTCAGTTA ACACTGCCCA GCAGGCAGTG TGGATCTCAA CACATCACTT CAACCCTTCT 1320
TTGGCTCTTC AGATAAACCC TCTGGTCTTC ACCACAGCCC TCCAGGCTCC TGCTCCAAGT 1380
TCCTTTTGTG CCTTTTTTCT CTTTTTCCTT CATGCCTCTG TCTGTTCCTC TAATGCTTTT 1440
TTTTCCCTGC CCCTGAGGAC CTTGGTTTGC ACCAGCCCCT CTACCCAGAC AGCTCTCTGT 1500
CCCGTAGCCA CCTGTGCATT ACTTTCCACT GCACATCAAA 1540
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