| Tag | Content |
|---|
EnhancerAtlas ID | HS176-02072 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr1:117031720-117032520 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXH1 | MA0479.1 | chr1:117032041-117032052 | TCCAATCCACA | + | 6.62 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_27848 | chr1:117031212-117033053 | Fetal_Intestine | | SE_28774 | chr1:117031372-117033147 | Fetal_Intestine_Large | | SE_50584 | chr1:117030703-117032338 | Sigmoid_Colon | | SE_50584 | chr1:117032406-117033514 | Sigmoid_Colon | | SE_52493 | chr1:117030787-117034097 | Small_Intestine |
|
| | 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 |
| GH01I116488 | chr1 | 117030630 | 117033982 |
|
Enhancer Sequence | TTAGATTTTT CCCTTCTCTG CTCATTATCA CTTTTCCTGA GGAGGTAACA AAATGTCTTT 60
TTCAATTTTC TTCTGGGACT AATTCTCACT GGGATCACCC ATTTTTTTCT CCAGTTTGCA 120
ACTGGCTAGA TTTGATTGGA ATAGATAAGG CCTCCGACCA TAGGCTGTTG AAAGGCCCTT 180
TGTTTGTGGA TTACAAGCGG TCATTCAGTT TATCCCATTC ATTATGCGAC CCTACTTTTT 240
TGAGTTGCAA GGTTAAGGCC TGGGGCAAAA TGTTGATGGA AAGGAACATT AAGCACCAAG 300
TAGTACCGTG TTTGTGTTCA TTCCAATCCA CATTCACCTC CCTTAACTGG TGAAGGTTAT 360
GACTACAGCC CACTCTCTAG TGACTCATTT CAGGAAAAGG ACATGTGACA AGAACCTGTC 420
TCACATGGGA CTGCTTGCCA GGGGTGCCAG GACAGAGATG GCATTGTTCA GGAAAGATTC 480
AGGAAGTCAA ACATCCGGAG AAAAGCATGC ATGGTTAACT CACCCCACAG GCTGGATGAG 540
AACATATTTT TTTTCTCACT GATCAATCTG TTTATCTACT TCTACAAGGG CACTCAGAGG 600
ACTTCTGGAA TAATTATTCC TTTTGGTCTT AAATGCAGCT TTCCTGATGG GCCAGGAAAG 660
GGAGAAGGGA TAAGTATTCC TGGAAGTGTT TTACCTGTTG TCACATTAAT TCTATCCTCC 720
CAATAGCTTT TTGAGATCAA CATTATCCCC ACTCTCAATG TATAAATGGG GCAATTTAGA 780
TAAGGCAAGT TAAGGAATTT 800
|
