| Tag | Content |
|---|
EnhancerAtlas ID | HS048-01167 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:44050600-44052580 |
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: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I043585 | chr1 | 44051165 | 44054319 |
|
Enhancer Sequence | GCCGCACCGC CCTATTATAG GGGGTTGTCA GCGCAAATAA TTAGACTTAA AAGTTACAGC 60
TGAAATATAA TCCAGAAATG GCAGGGCCCT GTTTTGGAAA TTGTCTATAA AATGTCAGCA 120
CTAAGGATGC ACAGGGAACG GTAATATACT GGCATTGTTG GAGCCTAAGA TTAGACCCTG 180
AGTGCATTTT TCCCAGCTCC AGTTTTTCTT TCCCTGCTGT TGCTTCTGTC AATAGACTGT 240
CCAGGGTGAG GCCTGTTCCT TTTTGGAGGC CCTGTGCCTG CAGCAGTGGG TGGAGGATGG 300
TTGGGGCTGC TGCAGTGAGA TGCCAGCCAC TCCAGCTGTT GGCATGGGGG TGGCTGTCTG 360
GGCAGGTCTA GGATGCGGGT CCCTGTTGGC ACTTGGAATA CAAGGAGGTT GTCCCTTGCC 420
TGTTTCCCCC ACCCTTCCTC TGTAGACATA CCCTGACCTC CCTCACATGG AAAATGTCTC 480
AGTCTCAGTA ACGTTTCTGC GTGGCTGAAG CCCAGTGTCC TTGTGAGAGT GAAGGTGGTG 540
TGCCCAGGAG CCTCTGGACC TGAGGCCCTT GCTTGGTGTT GCAGGTGACC CTAAAGGCCA 600
CTGTTGACCT CTCACACTTA TGCCTAGCCC CTAGAGCTCT CCCTGCCCCC TGCATCTAGG 660
AGGGAAAAAA TAAACACAAC TCTTCTGTGA AGCGCCTCAA TTTCCTGACA GCCGCAGGAG 720
TTGGAGGCTT TAGAAGACGT GGCTCAGGGC GTTGGCCTGA CCTCCAGGGC TGATCCATGA 780
AGTCCGCCTT TTGGCCTGAA GACCCTGTCC TCCAGGGACA ATTTGGGGGT AAAGTCCAGT 840
CAAGTTTCTA GGTTGGTGCC CAAGGTTTAT TGGCCAAGGA CCTACTTCCT TCTGCTGGGG 900
CTCTTTGTCC TGGTATCCAA CGACGTGATT AGGCCCCATG ATTCCACCAC CGACTGGGGT 960
CAAGCCTGCA ATCATGACCT CTCCCTGGCA CAGGCTGTCT AAACCCATCC TTACGCCCGC 1020
TGGAGCAGCG TCCTCTCCTG CCAGCCTCTG CTAATTCTGA TGCTTCTCCC CAGAGCCTTC 1080
TGGGTCTTTT TTCAGGCCTG TCAGCTAGGG CTCGAAAGGG TGACAGTTTT TCATCACACA 1140
GACCTACTCC TACTACGTAT ATAAACTTGG TCATGTGGCT TGGTTTTAAA ACAGTTCCCT 1200
TGACTGTAAT TGGCAGGTGA TAGCATCTAC AGCATGGAAA CCTGCACCTA GTAGGTGCTT 1260
AAGCATAGCT TCCCTTCCCA TGAAGAGGAG GAGACAGGGC ACCCACTGGC CGAGAGGACA 1320
GGAGAGATTT AGTTCATTAA GGCTGCTCCT CTGTGCTGCC CCCACCCCGC TTCTGTGGCA 1380
GGCCTGGACC TGATCTGCAA ACAGACTTGC CTGCCTGTGC CTGTCCCTGA GGCCCATCTC 1440
CAGAGCAGAG GGAGGGCATG CACCGCTGGG CTGGGTGGTG GTCCTGGCTG AGCCTCCTGC 1500
TCTCACCTTG GACCATTTGA GGTGCGTGCT CAGAGAGTCC TTTGTTGCCA TGAGACACTT 1560
GCCAGCCATG CCCCGGGATC CACCTGTTCT GCCACAAGAA CTGTGTCTGT GACATGCTGT 1620
CATCATTGGT AGAGACTCCT GGCACTAGAA CAGATGACAG AAACCCACTT ATACCAGCGT 1680
AAGCAAAACA AGGAAGTCCT GTGTTACAAA TCTGAAAAGT GTAGTAGATT TGGTGCTGGG 1740
CAGGGCTAGA TCCAGGTACT TAAACAGGTT GGCCAGTCAT TTGTCTGTCT GTTTCTGAGC 1800
TCTCCTCTCC TCTGTCGACA TCTTTGTTCT CAAGCAGCTT TTCCTGTGTG TTGGGAGAAG 1860
CCATCCCCAG CTGCTCTAAG CTTAGCTACC TCAGTAGAGA GAGAAGGTCG CTTTTCTAAT 1920
AGTTTCTGCG GAAGTCCAAA GGCTGTTTCT CCATAGTCAG ATCTGGGTCA CACACCCCAT 1980
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