| Tag | Content |
|---|
EnhancerAtlas ID | HS148-14783 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr5:138042160-138043400 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr5:138042190-138042200 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr5:138042190-138042200 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr5:138042190-138042200 | AATGGAAAAT | - | 6.02 | | ZNF410 | MA0752.1 | chr5:138042606-138042623 | GAATATTATGGCATGTG | - | 6.72 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_29550 | chr5:138043001-138046226 | Fetal_Intestine_Large |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr5 | 138042670 | 138043220 | | chr5 | 138042389 | 138042546 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I138707 | chr5 | 138042689 | 138043089 |
|
Enhancer Sequence | GCAATAAGGA AAAAGTCAAA AAGTCAAATA AATGGAAAAT CAACAACTTT TATTTGATCC 60
ATCAGAGAGC TGAAGTCACA GAACAAAATG CCTCCCTGAA AATGAGACAG ATGAATACGG 120
ATCAGTTTAT CTGAAACAGA AGCTGTTTCA GCCAGGAGCC AGTGGGAATG AAGTGCTGAA 180
ACATGGAGGA CGCTTAAAAA CATCACAGTG AGTGAAGGAA ACCAAACAAA AGATTACATA 240
GTGCATGATT TTATCCATAG GAAACGTCCG GAATAGGCAA ATCCATAAAG ACAGTAGATT 300
ACTGGTTGTC AGAGCTGACG GGTGACTGGT AATGGGTACA GGGTTTCTTT CTGGGGTGAT 360
GAAAACGTTC TGGAATTAGA TAGTGATGAT GGTTGCACAA TTTGTGAATA CGTTAAAAAC 420
CACTGAATTG TACATTTTAA AATGGTGAAT ATTATGGCAT GTGAATTATA TCTCAATTAA 480
GAAACAAACG TTAAGCAAAG ATAATTTGGG ATGGGAAGTC GAAATTTCCC TTCAAATTCA 540
GTTTGCAGAC CATTTTCAGG AACAGAAGGC TTTTCTACTG ACTCATGAGT TAGTAGTAGT 600
CAGAGCCCAG TCAGAGCCCA GCCTCTGACC ACCCTGCTCC CCTGTGATTT GCTGACTTGA 660
GAAGAGGAAG TCTGGGAAAT GGAACAGAGA GAGCCAGGAG TAGCCTGAAG AAAAGGAGCC 720
AGGACTGGGA AATGCTTGAA ACAGACTTCA GAGCTTTGTG ATGCTGGCTG AGGGCTCTGC 780
AGGAGGCCTT ACTGCTACAG CATGCCGCCA CCTCCTCCAT GAAGTCTCCC TGCCTCTTTC 840
TTCCCATAAG GCACTTTATC TGGCATACAT CGTTTTCACC CAAAGACCTC ACACTGGATC 900
CTTTACTGCC TTGTTGCCTT GCAGGTTCTC TGACTGTTCC ACAGAGAGCT ATTCTACTTG 960
GAGATATGTG TCCCCTCCAC AATGACATCA CAACCTCTTC CAGGATGGGA TGCCTGTCTT 1020
GGACTCACAG ACCCCCTTAA TGCAGGAAAA AACTTTAGGC ATCACCTGGC CCCCTCTTCC 1080
AAATTTAAAT GTAGCCCAAC TATGAGACAC TTGGGTTGAC TCGAGTCTCC CAGCCTCCTG 1140
GGGTCATCCT TCCCTCTGTG TTAAGCTAGA TGGACACGCA CTGCCCCCTA TCCCCATGTA 1200
CAATGGAAAA CTCATGTCCT GAATCCTGTG CCTTTGAGGG 1240
|
