| Tag | Content |
|---|
EnhancerAtlas ID | HS187-00364 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr1:24691370-24692780 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Crx | MA0467.1 | chr1:24692754-24692765 | AAGAGGATTAG | + | 6.62 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_26747 | chr1:24688147-24692955 | Esophagus |
|
| | 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 |
| GH01I024364 | chr1 | 24690723 | 24692812 |
|
Enhancer Sequence | TGTGAGCTGT TTGCAAATCA CCTAAGAATA ATGAATGTCT TAGAGGACTC AGCAGGCCAC 60
TTGGGGAAAG CATCTGAGAC CCTCCAGACA CTCCCAGGCA CACATTCACT CGCCTCAGGG 120
ATTCCCAGGG TTGGGAGGGA TAAAGGGGCA ATTTTTCTCA TCATTAAAGG GCAGCCGATT 180
GCCTCTGGGG TGGAATGCAG TATCTGTTTA ACAGGGTAGC GGGTGACAGA TTACAGCTGC 240
TTGGGAAGAA GCATCCCATA TCTAATTGAA AATCCCAGGG GAAGTTAGGG TGGGTCCAAT 300
CTAATTACCA AAATTGGAGT GGGGCCAACG GGGCTTGATT TTTCAGCTCT AGCTGTGACA 360
AGACAGCGTG TCTGTGCAAA TCCAGTGGCT TAAAACTCCA GGAAGCAGAT CAAGGGTTAG 420
AAAAATGGCC CTGAGTGTTG CACCTCCTTG CTGGGGAGCA TGAGTTGGAA GGCATTGCCT 480
AGGAGGAACT ATTTTGATCT CCAAAACTCT CACCCTGACT CACCCTAAGT GATTGAGTCA 540
TCACTGTGAC GGATATTGAA GACCTCAGAA GCGAAACCTT GGCTGATACT TCACTTTGCT 600
TCTGAAGACA CCCTGGAAGC TGAGAAGTCC TCTTAGCTTT GAGTCAGCAA GGTGGCCATG 660
GCCAAGGAAC ACCCGATGGC ATGACCTTTA GCTAAGGAGC TCAGAAATGC CAGTGCTAAC 720
AAACAGCCAG CCCCAAGCAC AGCATCCGCC CTGCGGGGCC ACACTAGAAA CCCTAGGAAG 780
ACACAGAGGA CCCGCTCACC TGCTTTGATA AAAATACAAG TTACCATGTG AATTTTGTGG 840
GTTATCTCCT TTTATCCTTA CAACCACATT ATGAGGTGTT CTTATCCTGG TTCACCAAGG 900
ATGACTTTGA ACCCACTGGG AGTTAAGTGA CCTCCCTTCC CCCAGGCCCA CAGGGCTGGT 960
GAGCAGGGAA AGTGGAGGTT CCATGGTACT GACTTTGGGG CCTACGCTAA TCAATCCACT 1020
GCCCACGCTG CCTCCATGGC CTCTTCAGGG GACGTGATCA GCCGTTCCCT GCCCTAATGG 1080
TGGCCTCCTG AGCTTTGGTC ATATCCAGCC ATCCTCTCAC GGCTGGGCTT TACATTTTTT 1140
GGCCAGTAAC ATGAGACTAA AAACTCCAGG GAGAATTCAT ATCTGCACTG ATGCTTCCTG 1200
CACCCTGAAG AAAGCAGATC CAGAAAAGCA TTTCTGTAGC TGTAACTCTG CCCAAGAATG 1260
GGAAGCCCAT CAACTCCAAC CCAAGACAGA TGAGGGCAGG TCTCCCCCTG CATGGCACGC 1320
GTGTGTTCCC GAGAAAGAAA CATGGCGGCA AGTCACCGCC GCTCCACGTA GCCGTGGAGA 1380
GCTAAAGAGG ATTAGTTCTG ATGTGGACAA 1410
|
