| Tag | Content |
|---|
EnhancerAtlas ID | HS095-15865 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr2:25328290-25329270 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr2:25328598-25328608 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr2:25328598-25328608 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr2:25328598-25328608 | AATGGAAAAT | - | 6.02 |
|
| | 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 |
| GH02I025105 | chr2 | 25328288 | 25329350 |
|
Enhancer Sequence | ATTACAGGCG TGAGCCACCA CGCCCAGCCC TCAATCTGAA TTTTTATGGC ATGGGTCAGA 60
GCTGCTTTCC TGTTCTACAT AAGTTGATTT AACCAGAAGA GAGTCTTCCA ACTTTCCTTC 120
CAAGGACCAA GAGTAGCAAC CTATACAGAT TCCCTTCTCT TTCCTCTCCC TGGGAGCCAG 180
CTGCCTTTGA CACATTACAC ATATACTAAC TGAGGGGAAA GTCCTTTGTC AAGTTGCTCT 240
GGCAACAGCT TCAGATACTG TTTTAGTTGT CCTGTTTAAG AGAACTACAG CCTAGAAGAG 300
AACATCTGAA TGGAAAATGA ACCAGCCACC ATGCATCCCT GGGGGCCACT GGAAGCAGGT 360
GGCCACCACC TCTAGCTTCC CCCACAGGAA ATCCTAGCCC AGGGTAGGTG TTCTGTCAGC 420
TACAGCATGA AAAATTCAGT GTCCTGCAGA TTCCCCATCG CAGTGAATCA TCGCATCAGC 480
CAGAGAGCAA GCTGACTAAT GATTGCTATG CTGCAGACAA TGAAGATGAT ATAAGGACAA 540
GCTATTGTCA GTGAGTTAAG TCAAATATTT GCAGTAGCTC CAGAGTGCAG CTTGGAAGGC 600
AGCCTTTTCT CTTGCTGTCC CTGTCTGATG CTCTTTCCAG CTCTCTGTGC CCAGACCTTC 660
TTGAGCCTTC CTGAGAAGAG TGTCCTTTTG CTCCTCATCG TTTTAGACCT GCTAGCATGC 720
TAGTGCATGA CATTATCTTA GAGTCTAGCC CGGGAGTTCC AAACAGGTCT TCACAGGGAT 780
TCAGGGCTTT GTGAGGGGAA AGGGGGCCTA GGAGAGGAGG AATAGAAGTC TCTAGGCCCT 840
TTACTGCTAC TTCATCCAGT AGCCACCTCT GGAGTTTTTT TTTTTTGAGG CAGAGCCTCG 900
CTGTGTCACC CCGGATGGAG TGCACTGGCA TGATCTCGGC TCACTGCAAC CTCCGCCTCC 960
GAGGTTCAAG TGATTCTTCT 980
|
