| Tag | Content |
|---|
EnhancerAtlas ID | HS158-22103 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr16:67248010-67249420 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr16:67248160-67248175 | TGGACTTTGGCCCTG | - | 6.63 | | Hnf4a | MA0114.3 | chr16:67248158-67248174 | TCTGGACTTTGGCCCT | - | 6.37 | | Nr2f6(var.2) | MA0728.1 | chr16:67248401-67248416 | AAGGTCAGGAGTTCA | + | 6.04 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr16 | 67248761 | 67248886 | | chr16 | 67248030 | 67248416 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I067214 | chr16 | 67248221 | 67248317 |
|
Enhancer Sequence | CGCCACTGCA CTCCAGCCTG AGCAACAGAG CGAGACTCCA GCTTAAATCA ATAAATAAAT 60
AAATAACCTG CAGGAGCCCA GGAACAGCCT TTCAGGGATA TTTCTCTGTG TGAGAGAACA 120
GCAGCAGGCT GAAGCAGGCC TTCTGGGTTC TGGACTTTGG CCCTGGTATA GGACACCCCC 180
TTCCTGGGCC CTGGGAAGAT GCTTCTAGAC CCACCCAAAG AGAACTGCAA GGCCACATGC 240
TCTAGCTCTA GCTGCCCCAT CTACAGAAGG AACACCTTGC CCCCTGGTCT CCTCCCTTCC 300
CGATGCTGGC ATCTTAAGAG TAACTGCTGG CCGGGCGTGG TGGTTCATGC CTGTAATCCC 360
TGGACTTTGC CCGAAGGCGC GCAGGTCACT TAAGGTCAGG AGTTCAAGAC CAGCCTGGCC 420
AACGTGGTGA AACCCCATCT CTACTAAAAA TACAAAAAAG CCGGGCATGG TGGCAGACAC 480
CTGTAATCCC AGCTACTCTG GGGGCTGAGG CAGGAGAATC TCTTGAACCT CAGAGGTAGA 540
GGTTGCAGTG AGCCAAGATC CTGCCACTGC ACTCCAGCCT GGGCAACAGC GCGAGACTCC 600
ATCTCAAAAA AAGGAAAAAA AAAGAGTAAT CGCAATATCA TTTGGGAACT GCTCTGAATC 660
TGCTACAAGT AACGTATGTA CCTTTTCTGT GGGAGACCAG GGTTTTGTTG TACCTAATGA 720
AGCCCTGAAC CGAGACTGCA GGCCTGTGTA CAGACTTGGA AAGCCATGTG ACAGAGAAAA 780
TGGCCCTTCG TCCTGCCTAA TACAGGACTC CAAAGCTACC GTGCTTGTTC TCCAGGAGGC 840
CGTTGGGAAA TGTACGCCCT GGCACCCAGG GCATTGGTCT CTAGAGAGGA GTTAGACTAG 900
TGGGTCATAC AGAGGCTGCT CCAGGACTTC ATCAATCCCT CAGGCAGGGA GGGCACAAAG 960
AGCTCTCTTC AGCTATTGCT TCATGGGGAC CAACCAGCAG AGACAACCAG GGCTCCCCCA 1020
GGAACGGACA GGGCCGGTAC ATATGGAGGG TGCTGCCTTT GCCGGCATCC TTATTTGAGA 1080
AAATTGGGAT TAAGGGAATA GGAGGGACTG GTCAGGGAAA GTAAGTCCCC AAGACCAGCG 1140
TCCTAGCCCA GCTTGGTGAG TCACCAGCTC TAGCTGGGCC TCGGTAAGCC AGTGTCTTCC 1200
ACAGCACCTA ACTGGTACCT AACTGCTACT GCCTCAGTAT CCACCTGCCC ATGCCCGAGC 1260
CCTGGGAGAT GGTTCCTGCC TGCAGGGTCC CGCAGGCGCT CTCTGGCACA TGGTAGGGGT 1320
GATGCCAGGT ACCTGTGGCC TGGCCTCCCA GTGCTCCCAG CCTAGGTGGG GCTGAGTTTC 1380
GCAGAGGCAC CAAAGGGTCT TTGTCAACAT 1410
|
