| Tag | Content |
|---|
EnhancerAtlas ID | HS180-01040 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:28213220-28214540 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr1:28214492-28214507 | GAGGTCAAGAGATCA | + | 7.23 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_09233 | chr1:28207973-28222018 | CD14 | | SE_20343 | chr1:28208587-28215125 | CD56 | | SE_50884 | chr1:28208283-28214544 | Sigmoid_Colon | | SE_53500 | chr1:28208262-28214990 | Spleen | | SE_62491 | chr1:28184415-28220281 | Tonsil |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 28213825 | 28214033 | | chr1 | 28213479 | 28214114 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I027881 | chr1 | 28208477 | 28220166 |
|
Enhancer Sequence | TGCGTGCCAG GCACTTACAA ACCATATCCA AATCCTCAAC TTTCCAGAAT GCCTGATTTT 60
AAAGATTAGG GAACAGGCTG CATGGTCAAG TACCTTAGGA CGCTGACAAG TTGCAGTTAA 120
GGGTGAGGAC CTGGAAAGTA TGAGACTGGG TTAGGATCCC AGCTTGCTAC CTACCAGCCA 180
GGGCTATGAG CAAGTTATTT TAACCTAAGT TTCAGTTTTT TGACATGTCA GATGAAACTA 240
TAGTTACTAC CCCAGAAGAC TGACTGTTTT AAGGATCAAA TGAGATAATC TTTGTAAACC 300
ATTTAGTACA GTGCCTAGCA CATAGTAAAC ATTCAACAAA CATGCATCAT TATTGAGCAA 360
GATCGTGTAG CTGTTCTGTC TCCAAAGCCT ATACTCTTTC CACCCCTCCA CAATGTTTCC 420
TAGTCACGGA ATACATCCCA GTGTTAAAAA TATACCATAT CCCTAGACTG TGGAGATAGA 480
GTATACTGAC TGGTTGGTGG GCCTCCCTGT CTTTAGTGGA GATAATACAA GCCTTTGTCC 540
GTGCAGAGAC TAACCCAGTT TTCAGAGGCA GTCAAGGCCC GTTCAGTGAG ACAAGACCAC 600
AGGCCACATT TCCTCTAAGT AGTGGGACTT TGGTTTATGG ACTGATGCGG TCACAGACAG 660
CAAAGGCAGG AAACAGACAA AGAGATGAAC TGAGACTCCA GCTGAGATGG GAGCCTAAAG 720
AGGGTGAGAT GCCCACTTCC TGGTTTCTAG GCATCGCCCC TGGGTGTGTC CTTCCTTTGC 780
TTAACATCTC CCTGGGCTGC CTGGACTCGC TGCACTTTTT AGCCTCCAGG CCTCCATACT 840
CCAGCATGGA GTTCTCCAGG TGACTACTGA GTGGCTCCTA CAGGCTGCTG GGCCAGTCAC 900
CAGGATCTGA CATCCCATCC TCATCTGCCC ACCAGCTCCC ATGCCCTTCT CCAGAGAAGT 960
CAACCTGCGC TGCAAAGGAG GACCCTGAGG AAGAGAGTAC CATAGGGAGA AGCAACAGGC 1020
AAGAAAGTCA GACAGAAAGT TCCTCCTTGG CACAGAATCC GGAGGGGCTA GGGTGATGCA 1080
CAAAATGCCA ATAGTTTTCA TTTCCACATT TGCATTTACT CTTGGCACAA AATTGAGCAA 1140
GATGAGTAAC AAAGCCACAA AAGCAGGGGT AAAAGAGGGC TACCAGTTCC TATAAAATGG 1200
GCTGAGTAGG CCAGGTGCAG TGGCTCACAC CTATAATCTC AGCACTTTGG GAGGCCGAGG 1260
CAGGTGGATC ATGAGGTCAA GAGATCAAGA TCATCCTGGC CAACATGGAG AAACACCATC 1320
|
