| Tag | Content |
|---|
EnhancerAtlas ID | HS180-01478 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:44050770-44053080 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Hnf4a | MA0114.3 | chr1:44051424-44051440 | GGGGGTAAAGTCCAGT | + | 6.24 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_23829 | chr1:44050776-44053120 | Colon_Crypt_2 | | SE_26649 | chr1:44050792-44053672 | Esophagus | | SE_27645 | chr1:44050342-44053172 | Fetal_Intestine | | SE_28595 | chr1:44050395-44053387 | Fetal_Intestine_Large | | SE_33537 | chr1:44045757-44056755 | H2171 | | SE_52524 | chr1:44050646-44053206 | Small_Intestine | | SE_65452 | chr1:44050722-44054192 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 44051923 | 44052290 | | chr1 | 44052345 | 44052640 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I043585 | chr1 | 44051165 | 44054319 |
|
Enhancer Sequence | TTAGACCCTG AGTGCATTTT TCCCAGCTCC AGTTTTTCTT TCCCTGCTGT TGCTTCTGTC 60
AATAGACTGT CCAGGGTGAG GCCTGTTCCT TTTTGGAGGC CCTGTGCCTG CAGCAGTGGG 120
TGGAGGATGG TTGGGGCTGC TGCAGTGAGA TGCCAGCCAC TCCAGCTGTT GGCATGGGGG 180
TGGCTGTCTG GGCAGGTCTA GGATGCGGGT CCCTGTTGGC ACTTGGAATA CAAGGAGGTT 240
GTCCCTTGCC TGTTTCCCCC ACCCTTCCTC TGTAGACATA CCCTGACCTC CCTCACATGG 300
AAAATGTCTC AGTCTCAGTA ACGTTTCTGC GTGGCTGAAG CCCAGTGTCC TTGTGAGAGT 360
GAAGGTGGTG TGCCCAGGAG CCTCTGGACC TGAGGCCCTT GCTTGGTGTT GCAGGTGACC 420
CTAAAGGCCA CTGTTGACCT CTCACACTTA TGCCTAGCCC CTAGAGCTCT CCCTGCCCCC 480
TGCATCTAGG AGGGAAAAAA TAAACACAAC TCTTCTGTGA AGCGCCTCAA TTTCCTGACA 540
GCCGCAGGAG TTGGAGGCTT TAGAAGACGT GGCTCAGGGC GTTGGCCTGA CCTCCAGGGC 600
TGATCCATGA AGTCCGCCTT TTGGCCTGAA GACCCTGTCC TCCAGGGACA ATTTGGGGGT 660
AAAGTCCAGT CAAGTTTCTA GGTTGGTGCC CAAGGTTTAT TGGCCAAGGA CCTACTTCCT 720
TCTGCTGGGG CTCTTTGTCC TGGTATCCAA CGACGTGATT AGGCCCCATG ATTCCACCAC 780
CGACTGGGGT CAAGCCTGCA ATCATGACCT CTCCCTGGCA CAGGCTGTCT AAACCCATCC 840
TTACGCCCGC TGGAGCAGCG TCCTCTCCTG CCAGCCTCTG CTAATTCTGA TGCTTCTCCC 900
CAGAGCCTTC TGGGTCTTTT TTCAGGCCTG TCAGCTAGGG CTCGAAAGGG TGACAGTTTT 960
TCATCACACA GACCTACTCC TACTACGTAT ATAAACTTGG TCATGTGGCT TGGTTTTAAA 1020
ACAGTTCCCT TGACTGTAAT TGGCAGGTGA TAGCATCTAC AGCATGGAAA CCTGCACCTA 1080
GTAGGTGCTT AAGCATAGCT TCCCTTCCCA TGAAGAGGAG GAGACAGGGC ACCCACTGGC 1140
CGAGAGGACA GGAGAGATTT AGTTCATTAA GGCTGCTCCT CTGTGCTGCC CCCACCCCGC 1200
TTCTGTGGCA GGCCTGGACC TGATCTGCAA ACAGACTTGC CTGCCTGTGC CTGTCCCTGA 1260
GGCCCATCTC CAGAGCAGAG GGAGGGCATG CACCGCTGGG CTGGGTGGTG GTCCTGGCTG 1320
AGCCTCCTGC TCTCACCTTG GACCATTTGA GGTGCGTGCT CAGAGAGTCC TTTGTTGCCA 1380
TGAGACACTT GCCAGCCATG CCCCGGGATC CACCTGTTCT GCCACAAGAA CTGTGTCTGT 1440
GACATGCTGT CATCATTGGT AGAGACTCCT GGCACTAGAA CAGATGACAG AAACCCACTT 1500
ATACCAGCGT AAGCAAAACA AGGAAGTCCT GTGTTACAAA TCTGAAAAGT GTAGTAGATT 1560
TGGTGCTGGG CAGGGCTAGA TCCAGGTACT TAAACAGGTT GGCCAGTCAT TTGTCTGTCT 1620
GTTTCTGAGC TCTCCTCTCC TCTGTCGACA TCTTTGTTCT CAAGCAGCTT TTCCTGTGTG 1680
TTGGGAGAAG CCATCCCCAG CTGCTCTAAG CTTAGCTACC TCAGTAGAGA GAGAAGGTCG 1740
CTTTTCTAAT AGTTTCTGCG GAAGTCCAAA GGCTGTTTCT CCATAGTCAG ATCTGGGTCA 1800
CACACCCCAT GTATGAAGAA TGCAGGTAGA AGTGGTTTCC TTAAAGACAA TGGGAATGCT 1860
CATTGATTTG AGGAGAAAGC AGAACCCTGA ATGTCTACAA GATACTCTCA TGCCCTAGGT 1920
GAACCTGGGG ACACAGATCC AGCCCACCAG CACCTGTCAG GCCTGGTCTC TGGGGCTGCC 1980
AGGGTTTGGG TTCTGTCTGG AGCACCAGAG TAAGGCAGGC TGTGGAAGGA GTTGAAGCAA 2040
GTGCTAAATT AGGTAGGGTC TCTTGGGCTG GGCAGAGGAG TCACTGGGAG CCATGCAGGA 2100
GCTTGTTAAA CAGGGAGTGG CATCAGATTT GTGCCAGCTG TTTGTGGAGG GCCCGTGAGC 2160
AGGAATTGGG GCAGTGGACA ACAAGGCAGG AGGACTGACG CAGAACACAT TGCAGCAACT 2220
CAGGGAAGGA TGATGATGGC TTGGACTTTG GTGGTGGCAG TTGCCTGTGT GTATGGAGAG 2280
AAATACATGG ATTTGGAAGA TATGTTATGC 2310
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