| Tag | Content |
|---|
EnhancerAtlas ID | HS145-07856 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr14:104159250-104160480 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SP3 | MA0746.2 | chr14:104160006-104160019 | TGCCACGCCCCTC | + | 6.08 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_24470 | chr14:104159192-104160636 | Colon_Crypt_2 | | SE_26911 | chr14:104159062-104160781 | Esophagus | | SE_32310 | chr14:104159095-104160464 | Gastric | | SE_41604 | chr14:104159140-104159852 | LNCaP | | SE_41604 | chr14:104159891-104160510 | LNCaP | | SE_60612 | chr14:104145010-104184512 | DHL6 |
|
| | 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 |
| GH14I103690 | chr14 | 104157271 | 104161386 |
|
Enhancer Sequence | CTCACACAGA CACATCAGGT TTACATCTGA AAGTACTGCC TCCCTTCCCC ATCACGGAGG 60
CCGTTTGAGT TTTCATCCAC TCCGCCCTTT GGTGTGGCTG TCAGTGGGTG GCCGGGTGCC 120
TGTGGCTGCT CTAGAACCTG TTTCTCAGGT GCCTGGGGCC CACCCGGCAG CTCGAGCTGT 180
TGGGACTTGG CAGTCCCTGC CCCTGTGCTG GTGCTGAGAG TTCGCGACAG TGGCCAGGCA 240
CTGCCCTCCC AGTTGTCCAG ATCCACTAAT CCTCACAGAC AGGCCAGTGC CCCGACCTGT 300
CCCCCAACAC TCTTGGGAGG CAGCCATCTC GGGAAAGCTT TTCCCCAGCC CCCTTCTCGG 360
TGGCTGTTAA AGAGGCTTGT AGGGTGCTGG ACATGTTGCT TGAAGCACCC CTAATGACAA 420
GAGGAAAGAA AGTCTCTTCA TTTTACAGGG TCCTGTAGCT GACCCAGTGT TTGCCCTCCA 480
GTTTCTTGGA GTTTCTACAT GCACATTGAC CCCTGGGCCT CTCGAGTGCC AACCTAGATT 540
TAGCTGTGCA GCTGGTACTG TTAGGCCTGA GGCCATTTGA AGCTGGCATC ATTTGAAGTC 600
CTGGTTAAGT GTAATTTTTC TATTTGTTTT TTCATGCAGG AACGAAATAA TTGTCTGGCC 660
GACTCGCGAG CTCTGAGTGC CAGCCACACT GACCTGGCCC ACTGAGAGCC AGCAGGGCTA 720
GGTAACCTGT CTTGGGAGTG TGAGACCGCC CCGCCCTGCC ACGCCCCTCA CCGCCCTGCC 780
CGGAGGCGCC AGCCGCACTC CTTGGCTTCC TTTCCTAGAT AGTGACGTCC ACCAACCTTG 840
GAGGTGCCTT TTCAAAACAC CCGGGAGGCC GTGCCTCAGC ATTCTGTTAC TCGGCCTGCA 900
GCCCCAGTGC CAGGAGCCAC CCCGACCGCG ACCCGGCCAG GCTGGCTCAG GGAGGCCGAG 960
GTGGCGCTGA GGTGGCTTCA GCACGCTGGG GATTGGCTCC TGCTCACGGA TGCTGTTGCA 1020
TTTCCTGCCT GCCACCTTTT TGCCATGACA CCAGACTCTC TTTTAAATTG TAATATTGTA 1080
ATAAGGCTGT AAATTAAGAA TCTGGAAACA TAAAGTACCC CTTTCAGAAC GATAGGCATT 1140
TAGTGATCTA TGGCAGTAAA GCCTGAAGCT TAGCGGACAC TGGTCAGTGG GAAGTGAATT 1200
CCTTCCCAGC TGGAGCATCT TCCGGGTCTC 1230
|
