| Tag | Content |
|---|
EnhancerAtlas ID | HS060-12594 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr16:21274650-21275920 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr16:21274724-21274736 | AAACAAACAAAC | - | 6.32 | | INSM1 | MA0155.1 | chr16:21275015-21275027 | CGCCCCCTGGCA | - | 6.74 | | KLF4 | MA0039.3 | chr16:21275809-21275820 | ACAGGGTGTGG | - | 6.14 | | ZNF263 | MA0528.1 | chr16:21274828-21274849 | CCCCTTTCCCTCTCCTCACCC | - | 6.07 |
|
| | 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 |
| GH16I021263 | chr16 | 21274814 | 21276525 |
|
Enhancer Sequence | GTTGGAGGTT GCAGCGAGCC AAGACTGCGC CACTGTGCTC CAAACCAGGC GACAGAGTGA 60
GACTCCATCT CAAAAAACAA ACAAACAAAA ACTCACCACA GCCTCAAACT CCTGAGCTCA 120
AGTGATCCTC CCGCCTCAGC CTCCCAAACT GTTGGGACCA CAGACGCCTG CCACTATGCC 180
CCTTTCCCTC TCCTCACCCC CGGTTCTCTC TTAACTCATG ACAAAAGAAA AAAAACAACA 240
ACAACAAAAA CTCAGTGTCA GGGTCATGGA GAAGTCTCGT CAGAAAGAAA ACTGGCTCCG 300
TCCTGGCCCT GAACTGTCAC ATCCTCTATG GAGTCCAGGA CCAGAATGAT GAATCCAAGG 360
TGTCACGCCC CCTGGCACCA GGACACAGGA GAATGCAGAG GCTGCCACCA AATGCCTGCA 420
AGGCCAGGGA GGTAATGAAA ATGAACAAAG CTGGTCAGAG GGACTGGATT AGATGTGGTG 480
GAGACTGAGG GGCGGGGAAG CCAGCAGGCC CTTCCGAAGG GGACAGTCAT TGTTCAGCTC 540
CAGCTAATCA TTACCACGTG TGAATGTAGA TCCACTGTTA CCAGATATGC CCCAGTTGTT 600
TTCTTAGAAG AGAAACAGGA AATCTATTTG CATATGTCAC TCCTTGAGTT TTAGATTACT 660
CTATGGTCCA AACCAAACAC ATCTGCTGGC TGGATCCAGC CCCTGGCTGG CTAGTCTTTG 720
AAAACTGCTA TAAAGCCTTA TACAAATATA AGACAGCATT TATATGCCTT CTTCCACTGC 780
CGCCCCGTTT TCTCCCTTTG TTCCCTCCCG TTCTGTTCTC CCTCATTCTA ATTTCCAAAG 840
AGAGTTGTGT AAAAATGTCC ATCTTGAAGG TTGTTTGTGC GGAGAGTTCT ATAGAACAAA 900
AGCACTAGCT TAAGGAAGCT TGTAAATAAA TCATAAGCTG GTGGGAACAA AACCCCCGTT 960
TCTCAGGCCA CTCCTTCTCA CTGGACTATT TCCCCTGCAC AACCACTGCT TATGAGCCGG 1020
GCGAGTTCTC AAAGGGTTGT GTGAGGTCAC TCAGGCGGAT GGAGGTGGGC CAGGCAGTAA 1080
AGAGAGAGAA GCCTGACTCA AACAAGGCTC TGGCTTGGTT GTGATGGGGC TAAATGAGTG 1140
AGGGTCGCAG ACAGGCTTGA CAGGGTGTGG GGGCAGGAGG AGGGAGGCAT GGGGCAGGGT 1200
GGAACTGGGC CTGTCCCTCC GCTGAGCTGT AAACTAAGTA AAATCTGTTG TTGGTATTTC 1260
CCTGTTGTCT 1270
|
