| Tag | Content |
|---|
EnhancerAtlas ID | HS187-13463 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr2:74792820-74794190 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HES2 | MA0616.2 | chr2:74792821-74792831 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr2:74792821-74792831 | GGCACGTGCC | - | 6.02 | | SREBF1 | MA0595.1 | chr2:74793838-74793848 | ATCACCCCAC | + | 6.02 | | TBX2 | MA0688.1 | chr2:74793600-74793611 | GAGGTGTGAAA | + | 6.14 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_45922 | chr2:74789220-74797514 | Osteoblasts | | SE_55945 | chr2:74792913-74796652 | u87 |
|
| | 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 |
| GH02I074566 | chr2 | 74793427 | 74796482 |
|
Enhancer Sequence | TGGCACGTGC CTGTAGTCCC AGCTACTCAG GAAGCTGAGG CAGGAGAATC ACTTGAACCC 60
AGGAGGCGGA GGTTGCAGTG AGCCGAAATC ACACCACTGC CCTCCAGCCT GGGCAACAGA 120
GTGAGATGCC GTCACACACA CACACACACA CACACACACA CACACACACA CACAAACATT 180
TGGCAAAATC CAACACCCTT ACATAATAAA AATGCTCAGT AAACTAGGAG TAGAATGGAA 240
CTTCCTCAAC CTGATAAAAA CCTCTATAAA AAAATCCACA GCTAACCTCA TATGTAGTGG 300
TGAAAGAGTG GATTCTCTGC CTCTAACATC AGAAACAAGG CAGAGATGTC TGCTCTTGCT 360
ACTTCTATTC ACTATTGTCC TGGGAGGTGT GCTGAAGACC AGAAGGTCAT TTTCCACATT 420
TTCTGTACTG TGTTAAGCTC TTTGGATTCT GGGTATGATC CTAGGGGTAG AGGCACCCAT 480
GAAGATATTG CGTGTGTCAA CATCCTGGCC CTTGGGAACC AATGCTTTCT AAATTTGATT 540
TAGAAAAATA TAGTAATGTG ACATTTCTCA TATCAGAGAG CTATGGTGCA AAAGGTCTAG 600
ATAGATGTGG CAACAAGTAC ATGGGTGTGG AAAGGCAAGA AAGATGAATG GGGATAGGCT 660
GTGGTGGAGG CAAGAAAGGC TTCATACCGA AATTATTTAA GCAGGATCTG GAAAAAAATG 720
AGTAGATATT TGTCAGGTAG ACAGAGGCAA AAGGAAGAGA ACAGCATGAA AAAAGGTGTG 780
GAGGTGTGAA ACAGTTCAGC ATATTTGGAG AACATTCAGT CATTTATTAG TGTGACTGGG 840
GGGAAGATGC GAGGGGCGTA GGTGAAAGAT GAAGCAAGAG AAACAGACAA AGCTAGGTCA 900
CAGGAAGCCC ACTGACTCAC GCTAGGCTGC TGTTCTAGCA CCTGTCTATC CCCCCCACCC 960
GCCCAGATGC TACACTGTAA CCTCCATCAT TCTGTTCTCG AATGGCTCCT GACCTGCCAT 1020
CACCCCACTC TCAGCTTGGA TTCTTGGTCT TGAGTCTTTG CCTATTTAAC CAAGCACTTT 1080
CCATCTCCCC ACCCAGTTAT AGCCCAACTG GCTCATTGCC TGTGTACTTA GACTCCTGCT 1140
GAACACATCA TGGCTTGAAT CCTGTAACTT CTGTGGCCAA TTAGGGCAGA CATGGACTGT 1200
AAAGCTCTGG AATGTGTCTC CAGAGACTCT GACATTTTAA GTAGGAAACT GAAAGACCTA 1260
GGTGGTATTT TCATTTCTTT TTCTAGTTCA CACAGACATG ACTTTGTAAT TGAAATGAGG 1320
ATGTGGAAAG TGAGTCACTA GCTACATAAC TAGGACTATA CAGCAAGATT 1370
|
