| Tag | Content |
|---|
EnhancerAtlas ID | HS044-00649 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr1:110502240-110503470 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr1:110502314-110502327 | GAATATTCTGGAA | - | 6.46 | | NR2F1 | MA0017.2 | chr1:110502767-110502780 | CTTTTGACCTTTG | - | 6.87 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_32320 | chr1:110502294-110502773 | Gastric | | SE_34099 | chr1:110500834-110504596 | HCC1954 | | SE_47194 | chr1:110500087-110506717 | Panc1 | | SE_50838 | chr1:110502272-110503454 | Sigmoid_Colon | | SE_53269 | chr1:110502238-110503062 | Small_Intestine |
|
| | 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 |
| GH01I109958 | chr1 | 110500903 | 110504624 |
|
Enhancer Sequence | AAACTCATTT GATTTCAAAG CATGTGCTCC AATTTTAACT TTTATTATCT TATTCTGAAT 60
AATCTGGGAG CTGAGAATAT TCTGGAAATA AAATCCAGGT TAGAGACCTG CCAAGAGCCT 120
AGACAGTGAG TTAAGCTGGG CTAAGGCACT GAGTAAACTC AGAAATGTCT GTTTGTCATC 180
TCCCTGTGCT TACTGCTCCT GTTGTTAAAG ATGTCTTAGC ATCTTAAACA ACTGAGCTTG 240
TGCTGAACCA GTGAACTACA TTGGGTGTGG GAGCTGGTCC TTGGGGGAAA AAAATCTCTC 300
CCTGCACCCA TATGTTTAGA AGCAGAAAGT TACCCGTGAT TTTAAGAAAG CTGCCTTTTA 360
GGAGACTGCC CTGGGCCTGG CTTATCACAT GAATACAGAA TACTGGTTTG CATTTCACCA 420
GCCTACATCA GATGTTTGTT TTAGCATACC ATACATTCTT AAAGCATGCG GGACAAGGAG 480
ATGCACTCCA GGAAGGGCCC TTTCAAAGTT TCGACTGGCT GTAACCTCTT TTGACCTTTG 540
CTCTAGTGCA CAGGCTCATC CTAGTCAAAG ACTTGTCTTC AGCATTACAA AATTTAGAAA 600
CCAACTCTGA ATTCACATGC ATTGTTTGCC AATGTTTTTC AAGTCTTCTC ACTTCCAGCT 660
GGATGGTCTT AAATGTACTC TGACCCACAC AGTTTCAGGC AAGTTGCAGA GCGCTTTGTA 720
GGTATCCGAT AAGTATGCCC TGAATTGAGA GGCTAATTAA ACAAGAGGAA TTTAGCAATA 780
TCACCTCTTG GCGTGAGTAT TATGTAGCAT CTGTAGTCGG GAGGGGTGGA GGGGTTGTAG 840
AGCAGGGGTG ACTTCTTTAA AACCTCTCAG TTTGCATATA TGCCTCCCCT ACGAAAAGTC 900
CTGCTGGTAA TAAACATAAT CTGCCCTGTG TGTTCCCACC ACAGGGGGGA CATATAGCAT 960
GAATAAGAAC TGGCTTCCCT TAGAGAGCTT TTCCAAAGGA CACCATCTAT TTACTCAGCA 1020
AATATTTACT GAGCAAAATG GGAGGAGAAG GGCATTCTGG GGAGAGAGAA GAGTTTGAAC 1080
AAAGCTAAAA AGGAGGGAAA ACCAGGAGTA TGTATGGGAT ACACTGAATA GTCAAATTCA 1140
GGTGATAAAA TCTGAAAGGT AGGAGGGAAC TGATAAGTAG AGCTTTGAAT GCGTGGCAAG 1200
GAGTTTGGAC TTACTGAAAC AGGCAAAAGG 1230
|
