| Tag | Content |
|---|
EnhancerAtlas ID | HS176-08670 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr12:6178490-6179490 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr12:6179454-6179467 | TTCCAGAATTTTC | + | 6.14 | | KLF4 | MA0039.3 | chr12:6178741-6178752 | GCAGGGTGTGG | - | 6.62 | | NFE2L1 | MA0089.2 | chr12:6178727-6178742 | CCTGCTGAGTCATGG | - | 6.7 | | Nfe2l2 | MA0150.2 | chr12:6178729-6178744 | TGCTGAGTCATGGCA | - | 6.96 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_27167 | chr12:6177956-6182148 | Esophagus | | SE_37940 | chr12:6174260-6186334 | HUVEC |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr12 | 6179429 | 6179488 | | chr12 | 6178600 | 6178800 | | chr12 | 6178640 | 6178845 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH12I006068 | chr12 | 6178015 | 6179350 | | GH12I006073 | chr12 | 6179458 | 6179526 |
|
Enhancer Sequence | GCTGCAGAGC CCAGAGCCCT TGATGCCACC TAAAACTGCC TCCCGGGTTG GCTCCTACCA 60
TTTCTCACAT GGCTGATGTC ATTCTAATCC TCCTCCAGGG GCTGCAGAGA AGCTCCGGCC 120
TGCTCCTCAC TTTACAAGCA GAGCCAAGCA TATCCCCTCC AGAACCATAC CGCCTATTCT 180
TCCCATCAGA AGCTCTATCT GCAGTCATCA CACTGGGAGC ATCAGACAGC CCCACTGCCT 240
GCTGAGTCAT GGCAGGGTGT GGAAATATGC TTGTGTGCGT GGGTGCAAAT GGACCGGGAG 300
GCGATGATCA ACAAAACTCC CAAACTAGAA AAAGATGGTC AGAGCCAGGG CTTTGAGAAT 360
GCAGAGAAGA GCGTAGTGGT TTTGTTGGCA AAATATCAAA CCACTTAGTA GACAGAATTG 420
ACACTGTTTA TCTTTTCATC AAGACATCAA GAGAATGTCT TACATCCTCA GCAAAGTCAT 480
CTTCTAGATT TTGAATTGAA GACCAGAGGA CTGTATTGTC TGCCCCAGAA AACAGTCCAT 540
CATGTACATA GTTGGTGTTC AAATAGTACT TGGATGAATG GACAGTTGGA AGGATGATGG 600
ACGGAAGATT CACCCTATAG TAAGTACTTG TTAAAACTTC CTAATCTGGT GGTTACAAAC 660
GTCTAAAAAA ACACACACAA TAAACTGAAT TCCTAATTCC ATCCACTGTG GCTCACAGAT 720
CTCATACAAT GAGTGCTTAT TATTTAAATG TTAAAAGTGT TTTCACAGGT TAATTGCAGC 780
AACTCATATG TCTTCCAAAG AGCTCCTTTA GTCTTGGACA TGGTGTAATT ACGTTCAGTG 840
GAGCACAGAT ATCCCTTTCA AGAGCAATCT TTTCTCCTTC GTGCCTTCTT TAAGGGTTAC 900
ACAAAAGATA ACCTGGCTGG GTGACCATCT CTTTGCAAGA CTAACTGATC TAGCCCACAT 960
CTAGTTCCAG AATTTTCCCA GTGTAGAGGA CACTGGATGA 1000
|
