| Tag | Content |
|---|
EnhancerAtlas ID | HS098-23387 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr17:16970010-16971090 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr17:16970868-16970878 | ATTTTCCATT | + | 6.02 | | NFATC1 | MA0624.1 | chr17:16970868-16970878 | ATTTTCCATT | + | 6.02 | | NFATC3 | MA0625.1 | chr17:16970868-16970878 | ATTTTCCATT | + | 6.02 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_23958 | chr17:16970054-16970378 | Colon_Crypt_2 | | SE_27670 | chr17:16969868-16971249 | Fetal_Intestine | | SE_37027 | chr17:16969513-16971449 | HSMMtube | | SE_46284 | chr17:16969924-16970928 | Osteoblasts | | SE_52055 | chr17:16970087-16970864 | Skeletal_Muscle_Myoblast | | SE_52535 | chr17:16970086-16971019 | Small_Intestine | | SE_63843 | chr17:16970049-16970893 | HSMM |
|
| | 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 |
| GH17I017066 | chr17 | 16970115 | 16970915 |
|
Enhancer Sequence | GTCAAACCCA CAGATACTTT TTTCATCTTT TTTTTTTTTT TTTTTTTTTT TTTTTTTTTT 60
TTTTTTTTTT TTTGAGACAG TGTCTTGCCC TGCCCTGTTG CCCAGGCCGG AGTGTAGTGG 120
TAAAAGCATA GCTCACTGCA ACCTTGAATT CCTGGGCTCA AGTGATCCTC ATGCCTCAGC 180
CTCCCACGTA GCTGGGCCTC TGCCAGCACT TGCCACCACA CCTAGCTATT AATAATTTTT 240
TTTTGGTAGA AACAGGGTCT TGTAGTTCCC AGGCTGGTCT CAAACTCCTG GCTTCATGCC 300
ATCCTCCTGC TTCAGCCTCC CAAATGCTGG AATTACAGGT GTGAGCCACC ACACCCAGCC 360
ATAAATACTT TTTCTATCTT ACCTGGGCAC TTCATCACGC ACAAGGGCTG TAACATTTGC 420
AGTTCGAGGT GTGATAGAAA AATTAGCATG AATTTCTTTT TCTTTCTCAA TTTCAGCGAT 480
AGAAGATTTA TTCTTACTGT ACATCTTAGC AACCTCAGCA TATGATTTTT TTTCTTAAAT 540
TGAAAACTTT TACCATTTCC CTTAAAGGAA GCACTTTATG GCTTCTCTTT GGCATATTCA 600
AATTGCTGTC ATCACTACTC TTGTGCTTTG GGGCCATTAT GTATAATACT AGCTGGATGC 660
ACAAGCACTG CAACACCACC ACAGTCCATC TGATAACTGA CAGCTACTAA GTGACTAAGG 720
GGCAGGTAGA GTATACAGCG TGGATGCGCT GGACAAAGGG GAGGCTCCAC ATCCTGGGAA 780
GATGGAGCAG GACGATGCAA GATTTCATCA CACTACTCAG AATGGCATGC AGTTTAAAAC 840
CTGTAAATTA TTTCAGGAAT TTTCCATTTA ATATTTTAAG GCTGTGGTTG ACCGTGGGTA 900
AGGGAAACCG TGGAACTGTG GATGGAGGAG GGGGGAACTA CTGTGTATTA ATGAGGAATA 960
TTAGTCCATA GTTCTTTATT TCATTTTTAA AAAATTTTGG GGTTTTGTCA TGTAATTTGT 1020
TTGGTTTTGG TGTCAGGGTA ACACCAGCTT CATAAAATGA ATTGGAAAGT GTTTCTTCTT 1080
|
