| Tag | Content |
|---|
EnhancerAtlas ID | HS007-16267 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr8:8966070-8967380 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYB | MA0100.3 | chr8:8966604-8966614 | GACAGTTGGT | - | 6.02 | | SOX10 | MA0442.2 | chr8:8967044-8967055 | TCCTTTGTTTT | - | 6.32 | | Sox3 | MA0514.1 | chr8:8967045-8967055 | CCTTTGTTTT | + | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_27764 | chr8:8965682-8967092 | Fetal_Intestine | | SE_28660 | chr8:8965442-8967304 | Fetal_Intestine_Large |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr8 | 8966447 | 8966966 | | chr8 | 8966486 | 8966781 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I009108 | chr8 | 8965552 | 8967023 |
|
Enhancer Sequence | TGGGCTCTTT GTTTTAAACT TCTGTCTGCA TTTTTGGAAA CAAGAGATGT AATTTTCTTT 60
CTTGAGAGCT CATCTGTGCA TTGAAAAACA TTTTTGTTGA AACCTTCTTA GTTGGCCATA 120
TTGCCAGGCC TAGAAATCCA ATCCTACTCA TTCTTCAAAG TTAAACTTTA AGCTTTTAGC 180
AGTTTCCTAT GCTAGCCCCT ACCTTTGTGC TTTGTAATAT AGACACTCAA CAAACTATTT 240
GTAGCTTTTG CATTCAAATG ATGGATTAGA AAAATGTTCT TTATAGTGAG GTGGTATCAT 300
TTTTGCTTAG TTCTGCCCCT TCTATGGTAT TCTCTTTTTT AACATAATAC CCTCTGTGTC 360
CCACTATATA CTTTTTACAA AGCTGGCTCT GGCTCAAGCC AAGGCCTCCT CTCTGGCACC 420
ATGGAATTTC TGTAGTGAGA TAGGAAAAAT CTATTGTGCT CTCAGAGTCA CAGACACTGA 480
ACAGCACAGC AGGGGCCAGG TTATCAGTGG CCTCTTCTTC CAGAGTTCCT GTAGGACAGT 540
TGGTTATCTC AGCCTGTGCC CAGTCAGCCT ACACGTGGGG GTCTGGGTAG TAAAAGCTGC 600
AGAGAAAGCA GCTCTGTCCA GATTCATTTG ATTAACTAGA CAGGCACATC AACTATACAC 660
CCGTTCATTG CATTGCAGTA TCCTGAAACT CAGGGGCACT TGAAGGGGAA GAGGAAGTAG 720
CTCCTGCCTC TGGGGTGCTT GTAATCATAT GGTAGTGAGA CACCCATATC CAAAAGAATG 780
AGAAGAAAAA TCCCAAGATG TTAGAGATGC AAGTGCCTCA TAGGGAGGTA GAAACTGTGT 840
ACACAATGCT GAGAGAACAT CAAGTAAAGA GAAGCAACTC CATTGGTTGG GACAGAGCAA 900
CATCATCCCT TGTTTCCTTA AATTGCCAGT AAATATTTAT CCTCTGCTTG CTTCTGCTTG 960
GGGCCAAATC ATTCTCCTTT GTTTTAGAGA GAAGGAAGGA GCCCCTCTGT TCTCCCCTTC 1020
CTGGGAAATT CATCGCACCA ACAGCGGAGA TCTTGGCTTT TTACACTATT TTGGGGGCTC 1080
TGCTTGGCAT AAAATAATAC ATTCCCTGCC TGGGGCTAGG ACAGATTGCT GCTTTTCTCC 1140
CACCTCCTGT AGGGTACATC TGGCCAACCA TCCCGATCAT TGTTTGCAAA GCTTCTATTC 1200
AAACATGTAT ATTGTTTTAT GAATGGCAAA AGAGGAAGCC AACAATAACC TTAGGTCTTC 1260
ATCTGCTTCT TTCATCTGAA GGGCGGGATG ATTCTGTGAA GTTCCCCTCC 1310
|
