| Tag | Content |
|---|
EnhancerAtlas ID | HS158-51431 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr7:29415000-29416400 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr7:29415974-29415989 | GAGGGGCAAAGGCCA | + | 6.22 | | Nr2f6(var.2) | MA0728.1 | chr7:29415030-29415045 | TGAACTCCTGACCTC | - | 6.22 | | RORA | MA0071.1 | chr7:29415708-29415718 | TGACCTTGAT | - | 6.02 | | Zfx | MA0146.2 | chr7:29415055-29415069 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I029375 | chr7 | 29414986 | 29417104 |
|
Enhancer Sequence | AGGGTTTCAC CATGTTGGCT GGACTGATCT TGAACTCCTG ACCTCAAGTG ATCCACCCGC 60
CTCGGCCTCC CAAAGTGCTG GGATTACGGG CGTGAGCCAC CGCACCTGGC TGATTTTTAT 120
TTCTTAACAT CTCACTTGAA AAGGTATATT CCCTTAATTA GTAGAGTTGG AATACTATGT 180
GGTATTGTTC ATTGTTTTAG AAAAAAAGAA CTGATAGCAT CGTGTGTTAC AACATGTGTT 240
CTGCCATCCT CCTCTAGCCT ATGACAGCTG GAACCCAAGA TCCCATTACT CATTGATCTC 300
AGGTGGTGGT GGTAGTGAGA GTGTGGATCC AAACTGAGAC ACAATTGTTA TGCGGAGGTA 360
CTGGCTTTTG TAACACCAAC CTTACTCATC CAAACACAGA GCAAATGTCA CACCTCCATA 420
GGAGTTGCTA CCTACAGCAG CCCCATATTA AGTCTGCTCT GTGACTCAGA GGTCAGGCCC 480
CACAAGTTTT GGGGTGTAAC CAGGGTTATC CAGGAAAAGG AGCAGGTGCA TAATGCTGGA 540
GCTATAGTGA GGATTTAAAG ACATGCTTCA CATTTTGCTC ACCTGGTTAA ACTGTAACTG 600
AGAAATAATG CTGATAAAGG CAGGTTATAC TTTGCTCCAG ATAAGCCATG TCTCCTACTG 660
GCGTGTGGCC TGTCCAACCA AGCACTGAGA GGCTTGGACG TAGATTTCTG ACCTTGATTC 720
TGCTTTCCAT TGGAAAAAAT GTGGATGATG CAATCTCAGA CAGCCTCAAT TTTAATATGA 780
CTATGCTGAA TGATATTACC TAATTATTTA CTTGTTGTCA GTCTTTTAAT AGAAATGACA 840
GCTATCACAT ATGGAGTACT TCCTGTGCCC TGAGCACCGG CTTCAGAGTT TTATGGATGC 900
TACGCCCACC ACAATCCCAT GGGGCTTGTT ATCCCTCTCA CTTTACACAG GAGGAAATGA 960
GACAGGAAGC ACAAGAGGGG CAAAGGCCAG ATTCCAACCC AGATAGTTCA TATCAATGGC 1020
TGGGCTTCTA ATCCAGTGAG TCACGGAGTG TGATCCCAGC ATCAGCTGGG AACAGGTGAG 1080
AAATGCAGGT TCTGTGGCCC ATCCCACACC TGAATTACAA ACCCTGGAGA TGGGGCCCAG 1140
CAATCTGTGT TTTAGCGAGC TCTTCAGGGG ATTCTGATGC CGCCTTGGGT GTGAGAACTA 1200
CTGTTCTAAG GACTGTTCTT GCTTCTCTCT GCTTTCTATT TCATCCTTCC TCCCTAATCC 1260
CTTAGGATAG AAGACTCAAG ATGCTTTTGC CTCCTGGTAA TGCTTGCTAT TTGCTCAGCA 1320
CTTGTGCTAG ACTATTCACG GATTTCAGTG TAGGCACCCA TAGCCTTCCT TATTTTTCCC 1380
AGATGTACTT CCTCCCAGAT 1400
|
