| Tag | Content |
|---|
EnhancerAtlas ID | HS044-05113 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr16:21274740-21276190 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| 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 | ACTCACCACA GCCTCAAACT CCTGAGCTCA AGTGATCCTC CCGCCTCAGC CTCCCAAACT 60
GTTGGGACCA CAGACGCCTG CCACTATGCC CCTTTCCCTC TCCTCACCCC CGGTTCTCTC 120
TTAACTCATG ACAAAAGAAA AAAAACAACA ACAACAAAAA CTCAGTGTCA GGGTCATGGA 180
GAAGTCTCGT CAGAAAGAAA ACTGGCTCCG TCCTGGCCCT GAACTGTCAC ATCCTCTATG 240
GAGTCCAGGA CCAGAATGAT GAATCCAAGG TGTCACGCCC CCTGGCACCA GGACACAGGA 300
GAATGCAGAG GCTGCCACCA AATGCCTGCA AGGCCAGGGA GGTAATGAAA ATGAACAAAG 360
CTGGTCAGAG GGACTGGATT AGATGTGGTG GAGACTGAGG GGCGGGGAAG CCAGCAGGCC 420
CTTCCGAAGG GGACAGTCAT TGTTCAGCTC CAGCTAATCA TTACCACGTG TGAATGTAGA 480
TCCACTGTTA CCAGATATGC CCCAGTTGTT TTCTTAGAAG AGAAACAGGA AATCTATTTG 540
CATATGTCAC TCCTTGAGTT TTAGATTACT CTATGGTCCA AACCAAACAC ATCTGCTGGC 600
TGGATCCAGC CCCTGGCTGG CTAGTCTTTG AAAACTGCTA TAAAGCCTTA TACAAATATA 660
AGACAGCATT TATATGCCTT CTTCCACTGC CGCCCCGTTT TCTCCCTTTG TTCCCTCCCG 720
TTCTGTTCTC CCTCATTCTA ATTTCCAAAG AGAGTTGTGT AAAAATGTCC ATCTTGAAGG 780
TTGTTTGTGC GGAGAGTTCT ATAGAACAAA AGCACTAGCT TAAGGAAGCT TGTAAATAAA 840
TCATAAGCTG GTGGGAACAA AACCCCCGTT TCTCAGGCCA CTCCTTCTCA CTGGACTATT 900
TCCCCTGCAC AACCACTGCT TATGAGCCGG GCGAGTTCTC AAAGGGTTGT GTGAGGTCAC 960
TCAGGCGGAT GGAGGTGGGC CAGGCAGTAA AGAGAGAGAA GCCTGACTCA AACAAGGCTC 1020
TGGCTTGGTT GTGATGGGGC TAAATGAGTG AGGGTCGCAG ACAGGCTTGA CAGGGTGTGG 1080
GGGCAGGAGG AGGGAGGCAT GGGGCAGGGT GGAACTGGGC CTGTCCCTCC GCTGAGCTGT 1140
AAACTAAGTA AAATCTGTTG TTGGTATTTC CCTGTTGTCT GCGCTTGTGA CACATTTTTC 1200
TTAAATGTAT GTGTTGCCTC TGTGAACACA TAAACCAATT TTGTCCCTGG GCCAGGAAAA 1260
CAGAAGAGAT GCCTTGACTC AAAATCAAGT CAGCCCTTCC TGGAGAATGA TTCCAAGTGA 1320
GAGAGGGATC CAACATAAGG GAGATTGTCT GTGGCTGGAT GTGAGGATGG AGAGTCCATA 1380
TGGTGGGAAA TTTGGGTCAT CTCTGGGAGC TGAGAATGGC CCCAAGGAAA GGGGCTCCCC 1440
CCATCCTCCA 1450
|
