| Tag | Content |
|---|
EnhancerAtlas ID | HS129-01734 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:117046980-117047840 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr1:117047152-117047163 | GATGAGTCACT | - | 6.02 | | JUND | MA0491.1 | chr1:117047152-117047163 | GATGAGTCACT | - | 6.32 |
|
| | Number of super-enhancer constituents: 13 | ID | Coordinate | Tissue/cell |
| SE_09543 | chr1:117044641-117049783 | CD14 | | SE_12587 | chr1:117046976-117047093 | CD34_adult | | SE_12587 | chr1:117047211-117047426 | CD34_adult | | SE_12587 | chr1:117047427-117047705 | CD34_adult | | SE_12796 | chr1:117047540-117047736 | CD34_fetal | | SE_20393 | chr1:117044944-117048752 | CD56 | | SE_27848 | chr1:117046065-117048119 | Fetal_Intestine | | SE_28774 | chr1:117046098-117048145 | Fetal_Intestine_Large | | SE_39920 | chr1:117043259-117048495 | K562 | | SE_41250 | chr1:117045162-117047933 | Left_Ventricle | | SE_50584 | chr1:117045995-117047955 | Sigmoid_Colon | | SE_52493 | chr1:117045201-117047975 | Small_Intestine | | SE_57245 | chr1:117046540-117047716 | VACO_400 |
|
| | 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 |
| GH01I116502 | chr1 | 117044918 | 117049421 |
|
Enhancer Sequence | AATACTACTT ACCTACTCCT ACTGAAGGGT GAGACGCAGC AGGCAATGCG CTTAGCACAG 60
GGCCTGGAAC ATAGTAAATG CTCAGTGGTA ATAGTGCATA GTCTTCCTTA AACTTGCAGT 120
GACATTTATT TCACCATGAT TAGCAGCTGA GGCTGTGGGG TGACATCAGG GTGATGAGTC 180
ACTTTGTCTG GCTGGGTCTT ACATCCGGGG CGATGTTCTG TTGCATCCAC CACCCTCCCC 240
TGCCCCAGCT CAGGGCCCTA ACAGTCTAGC AGGGCTGGGA CTTTCTGAAA GGCTCCCCTG 300
ACCACACCAG TTCCTCAGGA AGCCTCTCAA CCCCAGCTTC AGCTCTACTG ACATCGCCTT 360
ACTTCCCTTT AACCCCTTTT GAGGCCCAGT TTAGAATCTG TATCTCAGCC AGAGCTCTTT 420
CCATGCCAGC TTTGTCCACG CTGTTTACTC CTGGATAGTT CTCAGGCCCA GCCATATACC 480
AACCCAGTGC CTGCAGTCAG GCAGACCTGG ATGGAAATCC TGGTTCTACC ACTGACTAGC 540
AATGTAACCT TAACCATGTT ACTACTACAC TTCTATGAGC TTCTGTTTTT CCATCTATAT 600
AGTGGGACTA ATACTACTTA CCTACTCCCA CTGAAGGGTG AGACGCAGCA GGCAATGCAC 660
TTAGCACAGG GCCTGGAACA TAGTAAATGC TCAGTGGTAA TTCCAGCACT TTGGGAGGCT 720
GAGGCGGTCA GATCACTTGA GTCCAGGAGT TCAAGACCAG CCTGAGCAAC ATAGTGAGAC 780
TCTGTCATAA AAGAAAAAAA GAAATTGCTC AATGAAAGTG TGTGTGTGTG TGTGTGTTCC 840
TCCTGAGCAT TTTACTTTTC 860
|
