| Tag | Content |
|---|
EnhancerAtlas ID | HS044-00548 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr1:86077050-86078070 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFYA | MA0060.3 | chr1:86077750-86077761 | TCTGATTGGCT | - | 6.32 |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_02441 | chr1:86076209-86079638 | Astrocytes | | SE_37484 | chr1:86075848-86080255 | HSMMtube | | SE_39234 | chr1:86075703-86079642 | IMR90 | | SE_44599 | chr1:86071578-86081856 | NHDF-Ad | | SE_45004 | chr1:86075861-86079666 | NHLF | | SE_45832 | chr1:86071312-86080534 | Osteoblasts | | SE_47122 | chr1:86076320-86081209 | Panc1 | | SE_51901 | chr1:86076043-86079677 | Skeletal_Muscle_Myoblast | | SE_63698 | chr1:86076025-86079691 | HSMM |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 86077140 | 86077408 | | chr1 | 86077578 | 86077925 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I085604 | chr1 | 86070253 | 86080218 |
|
Enhancer Sequence | CTTGCCCTCA CAACCTTTGA ATTTCTATAA AGTGCTTTGT AAATGCCTTA AAGAGTCCAC 60
ATGTATCCAA AATTCATCTC CAGATGTATC TAATGATGAA AACCAGCAGC CCGGAGCTGA 120
GGTTTGTGTA AAGTTACATC AGAGTGAGGA GGGGGGAAGG AGCACAGCCT TCCCATTCTG 180
ATCAGTGTCT CTGTGGCCAC AGCTCAATAA GACTTGCTTT TTGAGGCCTC ATCCACTCAG 240
CCCAGAACTC AAATCTCAAA TTCCCCAAAC ATGAGGAATC ATGACAAAGC ACTGGTTTGC 300
ATTCTCTTGG CAAATGTTAC TTTAAAAGTA GAGTCAAAAC TACTTCCAAG TAAAGAGCAA 360
AGCAGCTTTA ACCAATATCA GCAAAGGGTC TAAGAAAAAA GATGTGGCTA ATGTATTCCG 420
TCTGTTTGTT TGCTTTCTTG TGCCCTAAGA CTCAGGAGAA AATATCAGTT TGGGAAAGAA 480
GTCATAACAC ATGGGGCAGG AACAAAATAC CAACAGAGCG AAGTTGCACA CGCTGTCCAA 540
CCTGGTGGCC TGCTTATGAA TTTGAAATCC CAGACCTTCA CATGAGTCCC CAGCCTCACC 600
CCATCCCTAG CCTGGCACAG ACAGGAATAT CTATTTCCAG ATATGAGCTG TTACATAGCA 660
GAACCAATCT GTACATCCGT GTGGGGCCAA TCGTCAGTGC TCTGATTGGC TCATCAGCCA 720
ACATGCAGGG CTGCATTCCT GTGGTTCACC CTTCCAGAAG GGCCTTTCCC AACACCACAT 780
GCTGCCTGTG CTGTGTCCAG CAGGAGAGGG GGAGGCAAAT GATGTGTCTC ATGGCACCAC 840
AGGCTCTGTT TTACCAGAAT AATACTGTTC TTTGGCCCAC TGCATCCGTT CTCCCCACAT 900
GGGCCTTTTC CTCACGTGGA CCCTAAAAGA CCACTTCTCT ATTTACCTGC CAACCTGTAA 960
CAGATAATTA TAGTGGCTGC CAGATATCCC TTCAAATTGG TCATGATCTC ATTCGGTTAT 1020
|
