| Tag | Content |
|---|
EnhancerAtlas ID | HS180-04314 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:207175690-207177100 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:207176164-207176185 | TGGGCAGGAAGGGGTGGAGGA | + | 6.36 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_26663 | chr1:207174076-207177334 | Esophagus | | SE_27711 | chr1:207174549-207176229 | Fetal_Intestine | | SE_31518 | chr1:207175680-207177145 | Gastric | | SE_33873 | chr1:207174470-207177225 | HCC1954 | | SE_34694 | chr1:207175413-207177474 | HeLa | | SE_57640 | chr1:207175746-207176266 | VACO_503 | | SE_57640 | chr1:207176309-207177226 | VACO_503 | | SE_57951 | chr1:207175743-207177070 | VACO_9m |
|
| | 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 |
| GH01I207001 | chr1 | 207174816 | 207177209 |
|
Enhancer Sequence | GGTATTGTGT TTTTAGCTTT TCTGAGAACC TTCATCTTGA TTTTCTTTGT CTCCTGTGAG 60
GTCTACATAA CAGGAGTGAT AATTTCCCTA TCTCATAGTC GAGGAAACCA AAGCCCAGGG 120
AAGTTATGGG ATTTGCTCAC ATTGGTGACA AAGTGAAAGT CCAAACCAAA GTATCTTGAC 180
CCTAGCAACG AGTAACTCCA ATTTCTCACA CCAGAAGAGG AGAGTGTTGA ATAGTGAGTG 240
TTGGGAATCC ATCTGATCCT AGTATGTTTG AACTGTGAAT ATGGCCAAAG TTTAGACCAT 300
TGGGTCTTAG TGGGTGGAAC TAGAGGAACT GGAAACTGGT TCTTGTTTCT CCATCTGTCA 360
CACAGAACCT ACCTATTAAT CCCATCCCCA GAAGCCACCC AGCCCCAAAG AAGCAAATGG 420
AGCAATGCCT GGGCTCAGGT TATGTAAGCA GAGGCTGGGC TGCCACCAGC CCTTTGGGCA 480
GGAAGGGGTG GAGGAGGGCC CTGCCTCTGC CCTTCAAAGG GTGAGTGTGA GACAAGAATG 540
TGGAGAGGCC ACTCTCAGCC AGGCCAGGTG GGTCTTGGCC TTGGAGCCAG CTCTGAACTG 600
ACAGGTTCAA ACCAATCTGT GGCTTAGCCT GCACTTCAGA ATGGGGTGGT GGTTGAAGGT 660
TTGTTTATTT GTTTTGGCCT TATCCCCACA CCAAACCAGA ATGTCCCATT GAGAAGGCAT 720
AGAGTGGATA AGACAGGATG CAGTGGGTCA GGACCAGCGT GCATCAGGAA GTCAGGAAGA 780
GAGGGTGCTC AGAACTGGAG GCTGCTTCTG CCCCTTGGAG CACAGGCCCC TGAAGTCATT 840
TTCAGGCCCA CACTCTGGAG TCTTTATTGG GAGAGTTTCA GGCATCAGTT TCCTGTAACT 900
CCATTCTGTT CTCCTGCATC ACCCTTGCTC TTTCATTTTT CTTCACACAG CAGCCAGAGT 960
GAGCCTCCAA AAACACAGAC CTGATCATGT CACTCCCAGG CCTAAGATCC CTAACGGCAC 1020
CCCACTGTGC ATCAAATCTG GATTCCTCAG CAAGGCCAGC AAGGCTTAAA GCAGCCCGCC 1080
TTCAGCCCCA CCTTGCCGCC TCTCCTGGCT GCTTGTTAAG TTCCAGTTTC TGAACAGGGC 1140
CCTCTGTTCT CTCACCCAGG ACTTTTGCAC CCTGCTGTTT CCACTGCCTG CCATTCCCAT 1200
TGTCCCCTTC CTTAAGCTCT TTCCCCTCTC TATTCCCACT TAGGTTATTC AGATCCCGAG 1260
ATCTGAGCTC AGGATCTTCT GCAGAGAAAT CTACTCTGAC ACAGTAGCCG GCATTAGGTT 1320
CCCTCATGGG CTCTCAGAGT ACACCATGCT TTCCCTATAT TGCATGTATC ACAAGTGTAA 1380
TTTACAATTA CCGTTGTTAC TGTCTGTCTC 1410
|
