| Tag | Content |
|---|
EnhancerAtlas ID | HS034-21438 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr3:123128220-123129440 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr3:123128450-123128463 | AGGAGCAGCTGCA | - | 6.15 | | ZNF263 | MA0528.1 | chr3:123129158-123129179 | TCCCCCTCCTCCTCCTCCCCC | - | 10.05 | | ZNF263 | MA0528.1 | chr3:123129009-123129030 | GAATGAGAAAGGGAGGGAAGG | + | 6.09 | | ZNF263 | MA0528.1 | chr3:123129184-123129205 | TTATCCCCCAATTCCTCCTCC | - | 6.28 | | ZNF263 | MA0528.1 | chr3:123129193-123129214 | AATTCCTCCTCCTCCTCCTCA | - | 6.38 | | ZNF263 | MA0528.1 | chr3:123129196-123129217 | TCCTCCTCCTCCTCCTCAACA | - | 6.6 | | ZNF263 | MA0528.1 | chr3:123129190-123129211 | CCCAATTCCTCCTCCTCCTCC | - | 7.01 | | ZNF263 | MA0528.1 | chr3:123129187-123129208 | TCCCCCAATTCCTCCTCCTCC | - | 7.21 | | ZNF263 | MA0528.1 | chr3:123129152-123129173 | GTTCCATCCCCCTCCTCCTCC | - | 7.29 | | ZNF263 | MA0528.1 | chr3:123129155-123129176 | CCATCCCCCTCCTCCTCCTCC | - | 8.95 |
|
| | Number of super-enhancer constituents: 14 | ID | Coordinate | Tissue/cell |
| SE_01550 | chr3:123127988-123129579 | Aorta | | SE_03867 | chr3:123128825-123146146 | Brain_Anterior_Caudate | | SE_04971 | chr3:123128740-123149524 | Brain_Cingulate_Gyrus | | SE_05846 | chr3:123127963-123154367 | Brain_Hippocampus_Middle | | SE_07929 | chr3:123128250-123134602 | Brain_Inferior_Temporal_Lobe | | SE_26038 | chr3:123127784-123136151 | Duodenum_Smooth_Muscle | | SE_26748 | chr3:123128718-123129516 | Esophagus | | SE_40589 | chr3:123127759-123154640 | Left_Ventricle | | SE_42153 | chr3:123127874-123129586 | Lung | | SE_46690 | chr3:123128738-123128936 | Ovary | | SE_47869 | chr3:123128079-123128765 | Pancreas | | SE_47869 | chr3:123128797-123129425 | Pancreas | | SE_48554 | chr3:123128036-123129657 | Right_Atrium | | SE_54494 | chr3:123127664-123146810 | Stomach_Smooth_Muscle |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr3 | 123128274 | 123129234 | | chr3 | 123128765 | 123129151 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I123409 | chr3 | 123127455 | 123134665 |
|
Enhancer Sequence | ATGTGGGGAA AAAGGACAGA CGGCCCAGCA CATGCTAGTT CTCAGGGTGG CCACTGGAGA 60
AGGTATCCTT GGAGTCAGGG TCTAAAGGTG GGATGCAGCT TTCACAGGTG GAAAGGATGT 120
GTTCCTGCTA ATAGTCCTGT CCAAGCAGCA CAGATAGGTA AGGGAAGCAC CACCAAAAAT 180
CCTCAACTGA TTATCTAGCA CAGTGGTTCT CCAAGTGGGA TATCCAGAGC AGGAGCAGCT 240
GCAGCATCAC CCAGGAAGCA GCTAGACATG CAAATTATTG GGCTCCACCT CTGACCTTGT 300
GACTCAGAAA CTCTGGGAGC CCAGCAAGCT CTCCAGGAGG TTAAGATGCC CACTCATGTT 360
GAGATGCCCC TCTTGCACCT CACCTGCTTC CTTAACAGAG GCCGGGCAGA AGGTAGAAAC 420
TGCCCCAGAG ACATTCCCTC ACTCACCGGC CCCTCCCACC CTCCAAGCCC CAGTTGGATG 480
AGCTGAGAAA GTTCCCTGTG GTTAGAGGAG CTAATCTATC ACCTGGATAT AAATTAACTT 540
GCCCTCTCTC GTCACCAGCC CACTGACCTG GGAAAGGCAA ACACGCAGCT GGCAGGGAAA 600
GAGCAGTAAT AAATCTCTTT TTCTACAGGT CCTCCCACAC CCACTTCCCC AACTGAGACC 660
TGTGTTCCCT GAGGCAGTGT GGCCCCATAG CCCTGAGGTC CCTCTGCTCT CCCACATGAG 720
CAGGTGCTGG ATCCGGTCAA CCCAGTGAGA GGCCCCCATC TGCCCTCAGG GCCTCCACCA 780
GAACTAGGAG AATGAGAAAG GGAGGGAAGG ATGGGGGCTG GAACACAGCT CATCACCCTT 840
AAGGATGGCA GAGTGACTGG AAGCTTCCCT TGTAGAACTC CTCAGGAAAC AGCCCACAAA 900
GACTCCCTCC AGGGCAGCTC TGTCTTGGCA GAGTTCCATC CCCCTCCTCC TCCTCCCCCA 960
ACCCTTATCC CCCAATTCCT CCTCCTCCTC CTCAACACAG CAGCCTGGGG CCACCCCGTA 1020
CCTCCCAGGC ATAAGTAGGA ATGGTAGAGC CATATCCCAA GGTGAACTGC CTGTTGGGGA 1080
AGGGCTAATC TCCTATTATT CCAACACCCT TGGCCACATC CTGCACTCTG TCTGCCTTTG 1140
GAATGACCAG GTGAAAACCA ACATAACGTC CACCTTAGAA AGCTGCAGTA AGAATGAAAT 1200
CTAACAGGAC ACATAAAGGA 1220
|
