| Tag | Content |
|---|
EnhancerAtlas ID | HS048-07058 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr11:69318890-69320880 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GFI1 | MA0038.2 | chr11:69319286-69319298 | AAAATCACTGCA | + | 6.11 | | HSF1 | MA0486.2 | chr11:69320474-69320487 | GAAGGTTCTGGAA | - | 6.3 | | ZNF263 | MA0528.1 | chr11:69319190-69319211 | TCCTCATCCCCGGCCTCCACC | - | 6.27 | | ZNF263 | MA0528.1 | chr11:69320098-69320119 | TGAGGAGGAGCAAGAGAGAGA | + | 6.44 | | ZNF263 | MA0528.1 | chr11:69320101-69320122 | GGAGGAGCAAGAGAGAGAGGG | + | 7.71 |
|
| | 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 |
| GH11I069504 | chr11 | 69319124 | 69320699 |
|
Enhancer Sequence | TCTTTGGATT TTTCTGTGTT CTTCAAATTT TTTTCCAACA AGCATGCATC ACTTTTATCA 60
CCCAAAAGAA TAATGGCTAT GTCTTTAGCC AGTGTCAGCG CACTGGGAGA ATTGCTGTGC 120
TCGGATGCCT TCTGCCAGGG TCTGTGCCTC GTCCCTCCCT GGGGTAGGAT GAGGGTTTCT 180
CAGCCAGGGT CTGGCCTCAT CCCTCCCTGG GACAGGATCG AGGTGTCTCA GCCACAGTGT 240
CATGGGCCCG TTGGGCCAAG TCATCCTTTG TTGAGGGGAG GAGCGGAGGC TGTTCTGTGT 300
TCCTCATCCC CGGCCTCCAC CTACAAGAGG CCGGAAGGGT CCCCTCCAGT TGTGACAAGG 360
GAGTGTCTCC AGATCCCATC AAACGCCTGT GGGGACAAAA TCACTGCAGG CTGAGAAACT 420
GATACAGATT TTTAAAACCC CACTTGGGGA CCCCAGCCTC CACCCTGCTT CTGACCGTGT 480
CCTCATCACA CTGAACATTA GTTGGGTGAA ACTTAAAATG CTCTCAACTA TCTGGCTGTG 540
CCGGCTTCAC AGAGCCAAAC CCTGCACCAC TGGAAAATAG TGCATGTCTA AACTCCATCT 600
TTGGATGTTC ACCACTGCTT CTGCAGGGCG AGGGCCCGGC TCTGTCACTC CTGAGAAGGC 660
TATTCCCAAA GTGGATGGAG CCCTGGGCAG GTCCCCTTCC CCTGCAAGGC ACCAAGAAAC 720
CAACAGGCAG TCCGCTCCTC GGAGGCAGCT CTCTTTTCAA GCATTCTTTC TGGTTTTCCG 780
TTCCTAAAAG GACGCTGCCT TTCTCTGAGC CTGTAAGAGC CCTCAAAGGG TCCAGCAGAG 840
GCCAGAAGGC TGAGCAGGGG CCTCCCTGGA TGAAGTGGGG AGTGGGGGTG GGGTAGATGC 900
TGCAGGCATG CCCTGCACCC ACCCACCTCC CAGCCATGTG CCCTGGGTGA GGCCTTCGCA 960
GGAACTCTGA CCCCTCTGCT TCCCATAAAG TGTTAGGTGT TGGTCTCGGG GAGCCTGGCT 1020
GGTGGATTAG TTCCTTCTCA AGCTGCTATA AAGAAACACC TGAGGCTGGG TAATTAATAA 1080
AGAACAAAGG TTTAACTGGC TCACAGTTCC ACAGGCTGTG CAGGAAGCAT AGTGGCTTCT 1140
GGGGAGGCCT CAGGAAGCTG ATGATCATGG TGGAAGGTGA AGGAGAAGCA GGCACCTCTT 1200
ACATAACCTG AGGAGGAGCA AGAGAGAGAG GGCGGGGAGG TGTCACATAC TTTTAAAAAC 1260
AACCAGATCT CGTGAGAACT CATTCACTAT CACAAGAACC GCACCAAAGG GGGAAATCTG 1320
TGCCCAGGAT CCAATCACCT CCCACCAGTA CCCACCTCCA ACACTGGGGA GTATAATTCC 1380
ACATGAGATT TGGGTGGGGA CACAGATCCA AACCATATCT GTTGGTTTAG CCACAAGTGA 1440
GCCCCTCCTG CCATATGCTG GGCAGCCAGG GAAGCTACCC AGGATGCCTC TGCCATCAGG 1500
GTCCGTCACT GTGAGCCCAG GGGAGGCCAT TGATGAAGGT GGGTGGGTGA GGCTTAAGGT 1560
AAATGAAGGT GGGGCACAAG GTGGGAAGGT TCTGGAACAT CTGGGCATAC TTCCCCATGG 1620
GGTGTACACC AGGAGGCACA GAGGGCAGCC CACATCACCA AGGGCCTCCA GTGGCCGGCT 1680
GACTTTAGGC TGAGTCGGCA GACCACACGC CCAAGAGTGA CAAGGCCAGT CACTGGAAGC 1740
GGAAGAAACG CTAGACATTT ATCCTTATTT TCTCAGACCT TTTTAGAAAT AACAGCGTTA 1800
TTGACCAAGA ATACCATACA ATTCATCCAT TTCCAGTGTA AATTCGGTGG TTTCGAGTAT 1860
ATTCACAGAG TTGTGCAACC ATCACCACTC CTAATTTTAG AACATTTTTA TCACCCCCGA 1920
GAAACCCCAC ACCATTAGCA GCCACCCCAC ATCCGCCGCT CCACTTCAGT CCCAGCAACC 1980
ACTAATCCAC 1990
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