| Tag | Content |
|---|
EnhancerAtlas ID | HS129-01698 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:114084170-114085630 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr1:114084921-114084935 | AAGGGATGACTCAC | + | 6.29 |
|
| | 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 |
| GH01I113541 | chr1 | 114084197 | 114085863 |
|
Enhancer Sequence | AAGTTCCTGC TTGCCTGTAA CGAGCGTGGC ATACTTAGAG AAATGTGTAG ATATAAACCT 60
TCTGAGTTTA AAACCTTGGA TATATTCTTT TAAGTAGGAG ACAGACTAGA AATAATGAGA 120
AAGCATTTGA ACACAGATGT GGAATATAGA GGTGACCAGA AAGAATATGT TGATAGTTGT 180
TAGCTTATGG GAATTGCAAA GGGTTTTAGT GTCAGACCTG AGTTAGTGGA TGTTCTTTTA 240
AATTATTGTT ACAAGGTTCT GCGTAACCTA CTGGTCTATG GAACTCTTAT CTCAGATTGT 300
GTGGACTCTT CCTCACTTTC TAAGAGCCAG CAACACTGGA TTTCTCTCAG TTCCTCTAAC 360
CACTGTGTTC TTCCCCAGCT CAAGTAAGTG CTGTCGCATG TCTTGTTTCC TCTACCAACA 420
TTTCCCCCAC TGCCCTTTTT GCCTTGCTGG CTCCTATTTA TCTTTCAGAT TTCAGCTACA 480
ATGGCACTTA GTGAAGTCTT CCCATAACTC CCAGATTTAG GATCTAAGTT GTAAATTCCC 540
ACAATACTCT GTACAGTAGT CCCCCCCTCC TTATTCTTGG GGGATATGTC CCAAGACCCC 600
CCAGTGGATG CCGGAAACCA TGGATTGTAC CAGATCCTAC ATATACTATG TTTTTTGATC 660
TAATAACCCA GACAGCTACT AAGATAGCTA CTGAGTAACT AATGTGTGGG TAGCATGTAT 720
GGCATGGATA TAGAGATGAT ACAGCAGGAC AAAGGGATGA CTCACATCCC AGGCGGGATG 780
GAACAGGACG GTATGGGAGT TGAGTTCATT GCAGCACTCA GAATGGCATG CAATCTAAAA 840
CTCATTAATT GTTTATGTCT GGAACTTTCC ATTTAATACT TTCAGACCAA GGCTGACTGT 900
GGGTAACTGA AACCGTGGAA GACAAAACGT TAGATAAAGA GGAACTCCTG TACTTCTCTT 960
TTATAATGTT TCCACGTTTG AAATTTCTTC TTCAATGTTT ATCTTCCCTG CAAGACTTTA 1020
AGTTCCCTTT GGGCTCACTC TCATTCACTG CGTTTAGCCC TAAGTACCTA CTCCTCAGAA 1080
CTCAGAAATG ACTAGACTGT GTCATGGAAA AGTAGGCTGT TATGAAACAG GAAACCTGTA 1140
CTCTATAAGC TTATGCAAAA GAAGAAATTC ATCAAAAGGG ACCATGTCTC TTACACACAC 1200
AGGTACATAC GCGTGTGCAC ACACACAAAC ACACAGAGAA AGAGAGAGGG AGAGAGAGAA 1260
AGAAACAGGG ATATTCTAGG ACAGCGCTTA CAATGTTTAC AGTGTAGGCT CTGAAGACAG 1320
ATTGACTGTG TTCACATCCC AGGTCTGTCA CTTACTAGCA GTGTAACCTT GGCCAAGTTA 1380
CTTGACTTCT CAATACTTTA GCTTCTTACC TATAAAATGG GAATAATAAT AACACCTACT 1440
TCAAAGGTTA TCATGAGGAG 1460
|
