| Tag | Content |
|---|
EnhancerAtlas ID | HS145-12917 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr2:97151240-97152480 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF2 | MA0051.1 | chr2:97151952-97151970 | GGAAAGCGAAACTTAGCC | + | 6.61 | | RUNX1 | MA0002.2 | chr2:97151283-97151294 | AAACCACAGAG | - | 6.14 | | SPIC | MA0687.1 | chr2:97152342-97152356 | GTCTTCCTCTTTTT | - | 6.22 | | Sox6 | MA0515.1 | chr2:97151896-97151906 | CCATTGTTTT | + | 6.02 | | Stat4 | MA0518.1 | chr2:97151946-97151960 | CTTCTAGGAAAGCG | + | 6.17 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_65729 | chr2:97150674-97152957 | 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 |
| GH02I096485 | chr2 | 97150742 | 97153281 |
|
Enhancer Sequence | GCACTTCACA CAGATCTGAG AGAAACAAGC TGGCTGCGCC AGAAAACCAC AGAGGCACCA 60
CCTCTAGATT CCTGTGGAGA TCCTACCACC CATTCCTTCA AAGGAAGGGA CTGGGGAGCA 120
GGGCAGCTGG CAGCAGAGGC TAATCTGCTG TGCAGGTCTG TGGAGGAAGG GACCGTGCGC 180
GGTTCTCTTC CCTCTGCCTC CAGGCTTAGG AGTCATCCCC CACACGCGGG ACCCCCAGTC 240
CCCACTGTAG ACTTCTTCCA AGTGGAATTT CTTCAACAGT TGATCAGCAG GGGGGTCAGG 300
GCGTGCAGTG CAGGGGTGGG GGTGGGGGTT GCGAGAGGAG TGCCATCAGG GAGTAATGCT 360
GGCGAGGCCT CATGAGGACA GCACGCTGGG GCCCTGTGTG CGATGGGCGC CAGGGGCAGG 420
TGACATGGTG GACCCGGTCT CCCCCTTCCC TCTCCAATTG ATCTAACAGA AAGCCTGATG 480
TGAAAGTCTG GACGAGGGAA TTTTCCCATA TCTGCAGGAA AGCCCCGTAG CAGGTCCCTG 540
GAGCCAGCCC GGGCAGGCCT CCGCTTACAG GACGCTAAAG ATCCCTGGTT GCAGTTCTAC 600
TTTCTTTTTA CTGCGTGTAT TCTGCCCCTG TGATAATGAT TCATTACACG CTTCCTCCAT 660
TGTTTTACTC CAGTGACCTC ACGTCAAGGG AACCTGTGAT CTCAGGCTTC TAGGAAAGCG 720
AAACTTAGCC GCAGCCTGCC TCTCTCCCAG CCTGCCTTAC AAGCACTGTG AGTTGCTGGC 780
TGGCCGAGGC CCTGGCAGAT CAGACCTCCT GCAGCCCCAG GGATGGCACG GGCACCGCCA 840
CTCACGCAGC CGGTAGAGCG CTCCTAGGGC AGGCCCATCT CGCTTCCCTC TCGCCTCTCC 900
CCCCCGCTTT TGCTTGGGCC AATCCGACCT CCTCACCTCC TCGTAGCTCC CCCAGCACAC 960
CTTGCCTTTG CCATCTCTGC ATGTGCCGCG CCTGCTGTCT GGAAGACCGG CATCCATTCC 1020
CCTCTGCCTT CCAAACTCTC CCTGTAGGAC CAGCTCAAAA GGCATCTCCT CTTCAGCTGT 1080
TCCTGCTGCC AGGGCTAATA TCGTCTTCCT CTTTTTTCCC CACTAGCGCT TCTTTGTCTA 1140
TTTTGGAGAG GTTTTGTTTT GGATAACTTT TTAATTGAGA TGTAACTCAC ATTATCATAA 1200
TATTCGTCTT TTTTAAATGC ACAGTTCAAT GGTTTTTAGT 1240
|
