| Tag | Content |
|---|
EnhancerAtlas ID | HS101-47237 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chrX:69439380-69440710 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chrX:69439983-69439995 | AAGTAAACAGAC | + | 6.52 | | FOXP2 | MA0593.1 | chrX:69439983-69439994 | AAGTAAACAGA | + | 6.32 | | Nr2f6(var.2) | MA0728.1 | chrX:69440689-69440704 | GAGGTCAGGAGTTCA | + | 6.22 | | PHOX2A | MA0713.1 | chrX:69439545-69439556 | TAATTAGATTA | - | 6.32 | | PROP1 | MA0715.1 | chrX:69439545-69439556 | TAATTAGATTA | - | 6.14 | | Phox2b | MA0681.1 | chrX:69439545-69439556 | TAATTAGATTA | - | 6.32 |
|
| | 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 |
| GH0XI070219 | chrX | 69439598 | 69440570 |
|
Enhancer Sequence | TGTACACACA CACACACACA CACACACACA CAGAATACAG GATAAAGGAA GCCTCACAAA 60
TAAACAAGGA AGAGGTGGAT TGTTCAATAA ATGGTGCTAC AGGGGAAGTA AGCTATTATT 120
TGGAGGAAAG AGTTAAAATG TCATGCCGTA TACCTAAGTG TATTGTAATT AGATTAAAGA 180
GTTTCATTTA AATCATCAAA CCATAAAAAT AACAGAATAA ACTGAAGGGA CTCTCAGAAG 240
ATGGGCTCAG GATTTAGAGT CCCTCTGCTT GCAGTTCCTT TGTGGTCTAT TCCCTTAAGA 300
GAAAACAGTG GGGCCCTCCT CAGAGCCTAC AAATGTTTTT CCTTGGCCCT GGTGCTTTCT 360
AGGCAGAAGC AAGACTCCAA CCCAATGGCA CAACACTACC TCATGTGCAG CAAAATCAGT 420
GGTCAAGGTC CCTTAGCATT TGTTGAGCTG AAAAGAAATG AATGGGGCCT CTGCTCAGGC 480
ATCCCTCAGG TGCCTCAGGC CCAAGCTCAC TTCTATTCTG TCGCTGCATA ACAAGAAAGT 540
ACCAAGAGGG ACAAGGGAGA GGTTGGATGT AATGTAGATA GGGGAACAAT TCCTTGTTGA 600
GGGAAGTAAA CAGACCTTCA GACTCACTGC TGCTGCCAGG TCCACAACTG TCACAGGGAA 660
CTCACTCTTT TCAGGCCTCC ACAACATAAA CCACCACAGT CTCAAGGCAC GATGTCTGAG 720
GAAGAATTAA AAACATTGAG AGCCTACATG CTGGCTCCCA AGACCTGGTG GCGCTTTTTC 780
TCAACAACCA GTTTTCCTGT TTTCCCCAGT AACTGGAAGA AAACAGAGCT TAGGGATGGC 840
CTTGGACAGG GAACTGGTGA ATCAGAAAAC ACAGCAGTCA TGCTGATAGC TAGAGGAGGG 900
CTCCACCCGC TTTACAAACC AACTGCCTGG AGGTGAGCCA GGTAACACAG CCCCAAAGCA 960
TCTGTGCAAA CAAGTCCTCC CTGAAGACAA GCAGAGTCTG GGAGATGCCT CACTCTTTAT 1020
CTCCGAGATC TGTCACACCA TATGACATAT ACAGGTCATT ATAGCACATG GTGTTTGTAG 1080
AGGATTAGCA GTTCAGCAAA TGTGTCAACC TGACAAATCA CTCAGTGCTT TCAAGTGATC 1140
ACTACCCTGT TCTTTGGTTA TTTTAACAAA TGCTTATGGA GTTCCTACTA TGTGGCAACC 1200
ACTGTTCTAT TAGGTTGGTG CAACCTAATA GAACTACTTT TGCACTAAGG CTGGGTGCAG 1260
TGGCTCATGC CTGTACCAGC GCTTTGGGAG GCCGAGGTGG GCAGATCACG AGGTCAGGAG 1320
TTCAAGACCA 1330
|
