| Tag | Content |
|---|
EnhancerAtlas ID | HS145-01617 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr1:153488040-153489190 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:153488263-153488284 | GGAGGAGGACTGGAAAGGGGT | + | 6.3 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_02992 | chr1:153487818-153488496 | Bladder | | SE_23261 | chr1:153487446-153489480 | Colon_Crypt_1 | | SE_23926 | chr1:153487791-153489348 | Colon_Crypt_2 | | SE_25303 | chr1:153487485-153489518 | Colon_Crypt_3 | | SE_28418 | chr1:153487633-153489575 | Fetal_Intestine | | SE_36529 | chr1:153487745-153488859 | HMEC | | SE_52579 | chr1:153487618-153489518 | Small_Intestine |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 153488459 | 153488748 | | chr1 | 153488088 | 153488813 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I153514 | chr1 | 153487077 | 153489449 |
|
Enhancer Sequence | AAAGCTGCAT CTGCACTCTT CAGTGCCAGG GAACTAAAGG CTGGGGCTTC CTATGCGAGG 60
TGCAGAGCTC CCAGAGGAGC AGGCACACAG ACCATGACAG GAGGCGGGGT AAGAGGCATT 120
CATTGAAAGG TGCATCTGTG TAGGATTCTT CCTAGCTGAA AACCCTAAAC TGAGCCTGGA 180
GGCAGGAGAG GGGCTTTCTG ATGCTGTGGC TCTTCCTTCC TGTGGAGGAG GACTGGAAAG 240
GGGTCCCTTG GGGCCCTCCC CAGCCTCCCT CATTCTTCTG GACAGAGGGC TGGGCTGCTG 300
TCCCCTGGAC TTGGGGAGGA CACAGGCAGG GAAGCTGGGT GCTCAGAGGA CAGAGAAAGG 360
ATCTCCTTGG ACAGCCCACT GAGCAATGGC AAGTGGCTCG CCAGGTTTCT CCTTCTCTGC 420
TCCCTGCTCT CTTGTCACAC CCTTCCTGGT ATGAAGCAAG ACAAGCTCCG GTAGTGAGCC 480
CCTCCCTGAC TCCCTCGCCC TAGGCACTGC CTATAATGGG GTGGGGCAAA ACAGCTCCCT 540
TCTCCCAGCT TCCTCTTCAG GCTCCACTGG GTCTGTCCCT GCTCACCACC TGGACTAGGT 600
CCCTAGGTGT CAGGACAGCT GGAGCTGTCT CCAGGTGTGT CATCATCACT GGCATCCTGG 660
CCACCCAGGA GCCATACCTA GGTATCCTAG ACCCCCTCTC TAGGCTCCAT CCTACCTCCT 720
CCCACCCTGT TACCCTATAG CCAACAAACC CTGCATGTTC ATCCTTGGGC ACACGTCTGC 780
CCTCTTCCTG CTACCCTACT CCACCCCAGG TCACATCCTC ATTCTCTCAC CGACCCAGGG 840
CACCAGCCTC CTGGCGGGGG GCTCTGCCTC CACTCCAGGA CCCCTTCTCC AGGCTCCAGG 900
TCTCCTTGAA GTCCAGGTTT TCATCACATC ACCATTCTGT TCAACCTTCA CCTACTTCAC 960
GGCTTAGAGA TGAGGCTTTC AAACATCTGT TTATTCCTAG AACCTTTCTT TAAAATAAAA 1020
CCTTATGAGG AAGCCTGATA TATGAAAAAT ACAGGGCTCT GGCTGAAATG GGGTAAGGGA 1080
CCAGGAGTCT CACCCACGTG AGCCACTACC CCCTCAAGAG GAAGCCCTTA AGTTGCCTCT 1140
GAAGATCCAC 1150
|
