| Tag | Content |
|---|
EnhancerAtlas ID | HS110-03998 | Organism | Homo sapiens | Tissue/cell | KATO3 | Coordinate | chr6:1042970-1045400 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| INSM1 | MA0155.1 | chr6:1043054-1043066 | TGTCAGGGGTCA | + | 6.18 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 2 | ID | Chromosome | Start | End |
| GH06I001044 | chr6 | 1043661 | 1043810 | | GH06I001043 | chr6 | 1043950 | 1045218 |
| Enhancer Sequence | AAAGCTTTCT TCAGCCAGGT ACGTGCTGGC TCAATAGTGC AGCAGGTCAT TGTTGAGTCC 60
TGGCAGTGAA TGGCTGGACT TTGATGTCAG GGGTCAGGGT TTAAAATTGC ACTCTGCTTC 120
CTGGGTAGAC TGCTTACTCC GAGACACCTG GATCTGCTTA TTTTATTGTA AAATGGGGAG 180
AATCACTTTT TAAACACCCC ACGAGAATAT CATGAGAGTT GAATAACAGG AGTGGTGCTC 240
GAGGGGCTGG GGCATGGCCG GCGCATGGCT GGCGCTGGAT GCTTGCTCAC CTCTCTCCCT 300
TCCATGCCTG AGAGATCCCA GGCCTCACAG TTCAGGCAAT GGTGCTTTCA GATGCTCATC 360
CCTGTGTTGT CATCTTCCCA AAAGGGTGAC TTTCTCTGAG CCAAACTAGT CCAGCTGCTA 420
AGTAAGAAAA GCATCTCTTT TTGATAGTAC TTAGATGTCG GGATGATTCA GGAAGAGGGT 480
GATCTGGCCC AGCCACAGGA CAGGGTACCC TGATAAGCGA CCCTGAGTTC CTCACCCTTG 540
CTGAGATGCT GGAGGACCCA GGTCAGTCGG GTGCCAGGTT GCTGCTGTGT GGGAAGCCTC 600
CTGCCTCAGA GACGCCTTTG ATTTTGCGTC GGTCTTGCTC ATTGTGGGCA GGTCAGCATG 660
TTGAGGCCAA CTGCACTAAG GGAAATGCCA TGTGGTGATT AGATTTTTCC TCTGGGTTCT 720
TCAGCATTTG GTCTTTCACC AAAAACACAT GTCCATGTGG CATGTTCCTG TCCTGGCTGT 780
CCTGCGATTC TACTGCTGCA CTCGGCACTC TCCCTCGTCC TCCCTGGAGC ACTCTGTACA 840
GCGTGTGCAG TGAGGGAAGT GATGTACGCT GTTTGGAAAT AGTCTGCTCA AGTCACTTCT 900
CTTCCTTTCT TTGTGTAATT ATCGGGAGAC ATGCCGTGTT TACCAGTGGT AAGCCAAGAG 960
GCATGTGCCT TACTTTGGAA GGAGTATTGA GGGAAATGTG GAATGTGGTG GAAATTAAGA 1020
CATCAAACCC AGGGACAGGA ATCCGGAAAC CTAAACCCTA AACTCCTCTC TTACACAGAA 1080
CTTCTGGCTA AACAGCAAGT AGCAACTCTG AGGATGTCAT GCTCTGAGGA TGGTAGTGTC 1140
CATTTCTAAT ATCATCTGAA TCAAATGTAA ATAAAATCTT CTTGAATCAC TTTGAGTACT 1200
ACTGAGTGGC AGACATAGAG AATGCAGCGG CTGGACCAGG CAAAGTTCCC TTCCCTCGTC 1260
TGAAATCCAT CTGGGAAGAT TGACATTGAG CAACAGATTC TAAGTGTGGT CAGGGCTGCA 1320
ACACATCAAA CCAAGGTATT GCAGGAACGT AGTTTAAGAC TCACAGGTTC AAAGGAGACT 1380
TCAGTTGGCT AGGCTCACAG AGGATCACGA GAAAATGGAG TCAGGCTGTT GCTCTGAACA 1440
GGTCTTGCCA AAATAGCGAG TGCCCATCGG AGACAACTTG TTTGAACCCC AGCACTGCCT 1500
TGATTGGGAG CTCAGTTGAA TAAACCTCCT GAGCAGGTGC AGCCCTGGGT GCTGAGCCAG 1560
AGCAGGGCAG GGTGGTCTCC AGTATCACTT CTCTAGGGAG CACATCCTGT GGATTTCCAC 1620
CCCGAGGTTC CCACAACTGG TGAGAGCCCA AAGTCTCCTG TGAGCAGGGC AGTGACCTGC 1680
AACTGGAACC ACCCTGGTCC ATGGAACACT CAGCTTCCTC TTCAATAGGT GGGTTCACAG 1740
GGGAGAGGAG CTATCAGGTG CACCATGAGC ATATTTTTCA GAACAATTGC TTTTATCAGC 1800
TTGGCTTTCT TGTCCCAGAA TGCAGTCCTT GGCAGGAAGT CACTGGTCTA TTGACTTTAC 1860
TAGTAGGATA AACAAACCTC CTTTGACACA CAGAATGGCA GAGACTGTAA TTTCCTTCCC 1920
GCCACATGGA GGCAAGGCAG ACGAAGTTGG GGGAAGCAAT GGGTTGGCTT TAACATGGAT 1980
TAAGAGCAAA AATCCTGGTT AAATATCAGG CAAAATGCTC CCTGTGTAGG CAAGAAGGGG 2040
TGAAAGGCAT CACTGGGAAG CCTCAAATCA GGAGGGCAAG GGAAGACAGT GCAGGAAGAA 2100
GAAAGGGTGG ATCCACTTTC TAGCTTCCAG GAGACATTTA CTTTGCACAC CGTGAAGTCT 2160
AAATGGGCTA TTTTTGTTAC AGGTCTGCAC TCCTAATCTA TTCTGTTTTA CTTGGTGAAA 2220
TGATTGCAAG TGAAGTTGGA AGACAAAGGA GAAGCGTGTC CGTAACTATG TAATGGGTAC 2280
ATCGAAAAGC AAGACTGAGG GGTGAAATCA TGAAAGCAAT GTTTACTTTT CTTCTACTAC 2340
CCTTTGAAAC CTTCTCAAAG AGGTTTAGAG GTATCCCTCC TTTGCTCCTG GATGAAAAAT 2400
CAGGCCATCT CCAAGACTGT CTGGTCACTG 2430
|
| |
|
|
|
