Tag | Content |
---|
EnhancerAtlas ID | HS095-15887 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr2:26290900-26292350 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ALX3 | MA0634.1 | chr2:26291298-26291308 | TCTAATTAAA | + | 6.02 | JUN(var.2) | MA0489.1 | chr2:26291638-26291652 | CTGAGTCATTTCCT | - | 6.73 | NFE2L1 | MA0089.2 | chr2:26291634-26291649 | CTTGCTGAGTCATTT | - | 6.88 | Nfe2l2 | MA0150.2 | chr2:26291636-26291651 | TGCTGAGTCATTTCC | - | 6.41 | POU6F1 | MA0628.1 | chr2:26290905-26290915 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chr2:26290905-26290915 | ATTAATTAAT | - | 6.02 |
|
| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_09566 | chr2:26289818-26294619 | CD14 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 26291005 | 26291914 | chr2 | 26291590 | 26291772 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH02I026066 | chr2 | 26289807 | 26293562 |
|
Enhancer Sequence | AGGTTATTAA TTAATCTATT TCAGAGGATG GTCAGGTGGC CTAGAGAATG CTGTCCTGGG 60 GAAATGACAT TTATACTGCT ACATGAGATA TGATTAGAAG TTAGGTAGAA GAACATCATT 120 CCAGGCAGAG GAAGTGGGCA CAAAAAGGTC CTTAGTAAAG GAGCTTTTTG AGTTCAAAGA 180 ACTGAAAGAT GATGTGTGTT GCAAATGTGA CTTGTGAGGC TAGCAGAAGC AATAGATGTT 240 GAAGACGTGG GTTTGAGCCA GATTGTGCAG AGCCTGGTAG TCCATGCTAA GGATTCGAAT 300 TCCATGGAAG GTTTGAGCAG GGATGTGACA TGGTTAGATT CAATTTTTAA AAGATGGTTG 360 GCCCAGAAAA TGTGGAAAAT GGATTGGAGT TGGAATTTTC TAATTAAAGA CTTATCAAAG 420 ATGTGTTTAA ACTCTTACTG TATACTATTT AATCTTTAAG GATTATGAGC GATTATATGT 480 GAAAATACCT GTCAGTGACT GTGACAGTGA GCCTTTAATT TTTTTTTTGA GGTGATCTTT 540 TTAGTGCCAA ATACATCAGA CAATCCTGAG CCAAGAGACA GAGTTCTGAT CATAGTTAAT 600 TTGGTTTGTG AGCTTGAGCA AGTCATTTAA ACTCTGAGCC TCTTTCTTTA TCTGTAAATT 660 GGGCGTGTTT GAGAAATGTG TGCTTAACTT TAATTGTGTT AATCGCTTAA CTCTGGTTAA 720 CATATGGGCT GAGTCTTGCT GAGTCATTTC CTCAGACGTT GTGGGCAAGG CTTAAAACCA 780 GCTAAGCAAA TTTAGTGATG ACACATTTTA CCTCTTCTGT AGAAGTCAGA TGAAAGAGCT 840 GTTTCAAAAA TGTTTCACTT ATTGTTTTCA TGCAGATTAT CTCTTCGTGG GGGAGAGAAT 900 ACAGTACACA TAGCTCAGGA ACTACTGATG CACTGCCTTC CATTTTAGTG GCAGTTTGAA 960 TTTAAGAATT TCTAGTTTGT CTTAAGCTTT TCTGTAATCT CTCACATATA TATTCTTAAT 1020 TTCAACTGAT AATTTCTTTC TTAATGTCTA ATATAGCCTA TTTGCCCTCT GAACAGCATT 1080 GAGATGCTTT GAAATTTTAA TGCCCAAAAA GTTGGCTTTG GTAAGGTGGT TTTCATTTCT 1140 GCAGTAGAAC CATGGTTGAG GCTAATGGTC CCATCAGCAT TAGCAGGCCT TTGGCTAGTT 1200 GCACAGTAAA CTGCATGTTT CCCACTAGTA AAAGAGATAA CCCCAACAGT TTTAGGATTA 1260 ATGCTGAGTT GTAGTGTTCT TTGGGATTTA CAGATTTTTT TCTATAATTT AAACTTTTTG 1320 AGACATATCC TGAGGATAAT AGAAGGGCAT TTAAAAAAAC TTCAACTGGC TGGGCTTGGT 1380 GGCTCACACC TGTAATCCCA GCACTGTGGG AGGATCACAA GGTCAGGAGT TTGAGACCAG 1440 CCTGGCCAAT 1450
|