| Tag | Content |
|---|
EnhancerAtlas ID | HS094-40010 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr8:17764580-17765970 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SREBF1 | MA0595.1 | chr8:17764944-17764954 | GTGGGGTGAT | - | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_20525 | chr8:17764392-17766067 | CD56 | | SE_54192 | chr8:17764636-17766123 | Spleen |
|
| | 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 |
| GH08I017904 | chr8 | 17762110 | 17766353 |
|
Enhancer Sequence | CATGCTCATT TGTTTATATA CTGTCTGTAG CTGCTTTCAT TCTATAACCA CAGAGTTGAG 60
AAGTTGCAAC AGAATGTATA GCATACAATG CTGAAAATAT TTAATATCTG GTCTTTTACA 120
GAAAAAGTTT GGTCAACCTT GTAGGGGAAC CAGCCCGCTA TACCACCCGC GGGTTCTCCC 180
CTTCCCAGTG GAGACGAGGG AATGAGAAAA GAAATAAAGA CAAACACACA AAGTTCAAGA 240
GTTAACAAAA GTGGGTCCAG GGGTCCATCG CAATGTGGAA ACTGCGACAG CCCTGAGCTC 300
TGGATTCCAC TGATATTTAC TGAGTACAGT TCCTTTGATC CTATAGGCTG AGGGTGGGCA 360
GATGGTGGGG TGATCACAGG GTGACCATGG GGAGAGGTGG CAGAGGGGGT AGCATGCGTC 420
ATCAGCAAGT TAATATTATT TACTGTTCCA CTGTATAAGC TAATACTCTA TGTTTAACTT 480
ACAGATAATC CTTAAAGTCC AACTAATTGG TTAACAGAAC AGGACGTGAA AGCAGACAGC 540
CCGTCAGACC ACAGGCCTGT GCATCAAAGG AGCGGTCCAC TCCAAGCACC ATCAGCAGGG 600
CAGCAGAGCT CTCTGCCTCT GGGAACGAGC GAGAGATAGA AGACTTTCCC CTTATCCTCA 660
GAGGACTTCT CCTCTTTTAC AAGCAACCTC CTGCTGTTCC CTTCTGGGGA ATGGAGCAGG 720
GGTCGCTTCC CTTCCCACAA GACCTTTGTT CAGGGACTCA AGTGGGAGGT TGAGCAATAA 780
GCAAGCTTTC TTGCTTAGAG GCTCCGCACA CTTCCTGTGG TTGTTTGTTC CACCCTGCAG 840
TTAGGCAAGC AAGCTCACCG CCTGATTCTT ATATTGTCGG ACTAAGCAGA AGCTATTCTT 900
ATGATTCATG ACTATATTAA TAAAGCACTA TTCTAAAGCA TATTTTGTTA ATCCTTAAAC 960
AGGCACACCA TAGGCCAGCC CTCAACCACC TCGGCCCACA TCCAAGCCCC TGTTTTGACC 1020
CACATTTCCC CCATTTTTTA AATTTAAAAC AGCCATCTCA ATCATAACTT GCTTGTGGTT 1080
TTGATTTTCT TTCAGGAGCT GCCTTCCGCA TCTGCAGACT AAAAACAGAC AACATAAGCA 1140
GACACAAATT AAAACAAAAT TAGCAATGGC AGAGCTTCCC AGAGTTTTAA TCCATTTGAT 1200
AGAATTGAGC TCCGAGAGCC TATCTGCAGC TCCAGCAAGC ATTTCTGCTC CAGGCAACAA 1260
ATTTAAGTGA GCCTGCGATG CTGCAAAAAT CTGTTCTTTT AATTTAGTTA TATCCAGGGT 1320
TAGATTATCT TCTCTTCCTT GTAAGTGGCA TCAGACCTTT TCCCACTGAT GTTCAGTAAC 1380
ATTATAAGAA 1390
|
