| Tag | Content |
|---|
EnhancerAtlas ID | HS180-23636 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr19:8093100-8094800 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr19:8094112-8094127 | AAAGGCCAAAGGTCA | + | 7.01 | | Nr2f6 | MA0677.1 | chr19:8094113-8094127 | AAGGCCAAAGGTCA | + | 6.73 | | RREB1 | MA0073.1 | chr19:8093678-8093698 | TGGGGTTGGGGGGTGTGGGG | - | 6.22 | | Rxra | MA0512.2 | chr19:8094113-8094127 | AAGGCCAAAGGTCA | + | 6.09 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 8093129 | 8093432 | | chr19 | 8093472 | 8094571 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I008028 | chr19 | 8092970 | 8095351 |
|
Enhancer Sequence | ATTTACCCAG ATCCCCACTG CCTTTCCTTC CTGTGGCTGA CATCTCCCTA CACTGTCCCC 60
CAGAAACACA GCTGTTTTGC CCTCAACCAC AGCTCCTGCA TCCAGTGCAG GGCCTGGCTC 120
TTGACTGAGA CATCAGCAAA TGTGAGCCCT GCTCTCCTGG GTCAATGCAG GCTCCTTCAG 180
GAAGGAGGCG GGGATCTGTC CCCCTTGGCA TCCCCAGTGC CCAGCATGGG GGGCCTGGCA 240
CCCATGAGGC AGCCAAGGCT TTCAGACCAA ATGAACAAGC AGTGAGCCCT GCCTTCGAGG 300
GCCCGTCTTG AGGACACCAG GTGGGTTTAT GACATCCCAG TGGACATGAG GCCCCCAGGG 360
ACCAGTTCCT CTCCGGCATT GGCACCAGGG CCCCTGCCCC ACTGGATCAG ACCTCCCAAG 420
CTTGGGGTCC CTTTTCCAGT AGGCAAGAGA GGCACCCGAC TCCTGCTTCA GCCCAAGGAG 480
AACCTGCCGA CTCCAAGGGG TGGCCATTGA GGGGATCAGT GACGTAAGTC CTTCAGAGGC 540
AGCAGGGACA AGGAGCTGTA GGGAAAACAG GGCAGGCCTG GGGTTGGGGG GTGTGGGGTG 600
CTGACAAGGT GCAGACCCAC CACCCCAACC AAGCCCCTCC TCCGCAGATC CATCACCTCT 660
GCCCCGTGCC CCATGAATGA ACCAGCTCAT TCCCCGGCCC AGTGACCAGC ACAGGCTCCA 720
GACGTTTCCC TCGGACATTG TCTGCCTGAC CACCTCTTCC AGCACAGTGA GGGGCCTGGG 780
ATCTGGAGGC CAGAGTGGGC CAGGCCTAGG GGTGGGGGGA AAAACGTCAC TATTCTTAGA 840
TCCCTCGTCC TCCAGGGCCC AGGCCAGGCG GAGCAGTCAC ATTCCAGAGG TAGAAACCAT 900
CAGCCCACAC AAATGCTTGT GTTCCCTGAG GAGGCCAAGG GTCACCAGGA ACTAAAATCA 960
GCTTTTCCCA AGAAAGGCGG GAGACAGGGT GGGGGGCGGG GGGCAGGGTT AGAAAGGCCA 1020
AAGGTCACCC AATAAACCCT TCCAGCTGCC CCTGGTGGAA AGCCCCTCTG AGTCCGGAGG 1080
GATGAGGACA GAGGGATTCT CGCCCTCTAA GCTACTCTGC GGGCTGGCTG ATTCTTCCTG 1140
GTAGGGGGCG GTCCTGTGCA GTCTAGATTA TTTAGCAGCT CTCTGGCAGC CCACCGCCCC 1200
CCCAGCCTCC CAGTGGTGAC AGCCAAATCT CTCTCCAGGC ACGGGCCAGG TGTCCCCTGG 1260
GGAAAAATCG ACCCCAGATG AGAACTGTAC TTTCCCAAAC AGAGCTTCCA GGTGGCGTCT 1320
GGGGTAGATA TTTAGGATCC TGCTGTTCTA TGGACTCTGT TCTCTCAGCC TGGAATCCTC 1380
TTCCCGCATA GCACAATCCC CCACCAGCCC TGCAATCTTC CAGAACTAAA CCCACACATC 1440
ACCTCCCTCA GGAAGTGTCC TGTGGGCCCC CCATCTTATG ATTTTGGCCC CCACGGATGC 1500
TGTGGTAGGT AAAATAAAGC CCCTTTGGCC AGATATGGTG GCTTACACCT GTAATCCCAA 1560
CATTTTGGGA CGCCGAGGAG GGAGGATCAC TTGAGCCTAG GAGTTAGAGA CCAGCCTGGA 1620
CAACATAGCA AGACACAGTC TCTACAAAAA AAAATAAAAA AATTAGCTGG GGCTGGGCGC 1680
GGTGGCTCAC GCCTGTAATC 1700
|
