| Tag | Content |
|---|
EnhancerAtlas ID | HS018-11926 | Organism | Homo sapiens | Tissue/cell | CD19+ | Coordinate | chr2:11841420-11842790 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr2:11842609-11842620 | AGCCACACCCT | + | 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 |
| GH02I011701 | chr2 | 11841425 | 11842690 |
| Enhancer Sequence | TGGCTATGAG TAACTCAAGT GATCCTGTCT TAGTTATCTT CGTAATTACC CCACTGATGA 60
ACTCAGTGCC TAGCACAGGT CATGACACCT GATAGATGCT CAATGAATGT GTGACTGGAC 120
TTGCCTAATC CAGTCCCTGC TGGTCTCTCT GCTCTGAACC GTGACAAACA CTCATGCTTG 180
TCACAGCGCC GGCCCAGGTG GCACACACAG TAGACTCTCA ATACAAATGA GTTAATGCAT 240
CATACTGTTG CTATTTAGTT CTATGTTTCA GTAGTAGTAG TAATAAAAAT ATGACATTAC 300
TGAATGCATA CTATGTACTA GTTTCTATAC TAAGTACTTT ACCCTCATTC TCACTTAATC 360
CTCACGACAA CAGTACATCA TCATCTCCAT TCATGAAAAA TGTGAAGCAA AGAAAAGTTA 420
AATGACTAGG TCGAGGTCAC ACAGATAGTG CCTAGTGGGC CTAGGATTTG AGCTTAACCA 480
GTCCGATTCT AAAGCCTGTG TGTTTAGATT ACAGAAAGCT GCTGGTATTA TCCGTGGGTG 540
TAGCCGGGGC TGCCATGTCC TTTCCTACTG GCTGAGTGTC TGTTTGGTTT GGTCCGTGCT 600
TGTGCTAAAA CTCTTCCTGA ACTATTCTGT CTAATCCCTC CTGCGTATGT CAACTTTCTG 660
ACGTCATTGT GCTCATCTCT GCTGAGTTCT GCCTTCTGGT CTTGTGGCTG TCGGATGCCA 720
AGTGTCTTAA GAGTACTAGA GATTTGTTTT AATTGGGTAT GGGAAGACAG ACAGGAAAAT 780
GACTTTCACG AAGGAGGAAG TTTGTGGTGC TCACGGGTCC CTAAAGACAG GAGGCACGCC 840
ACGTCACACA AGGCCACATG GGGAAGCACT GGGTTGGTCA CGAGGCAGAG AGAGCAAAGG 900
GAAAATGTGG ACAAGAGTCT TTATTGTGGT TTCTGTGGAA AGGAACAGGT GAGGCAGGGT 960
AAACGGGCTT AGGGCTGGCT AGTGTGAATA ATTTCAGTGG GTTCCGGAGT ACACAGGCTG 1020
TCCCTAGTTG TCTGATCCCA GGCCCTGGGG TGAACAGCAC AGTGGATAGT GGCCCAGAGG 1080
GTGACGTCCT GACAAAAGAG GTGATTGGGG TCTGGGCTCT GGACTGGTTG GTTTGCATGT 1140
GAAAGGTGCA CTCACAGACA AGGCCTGGCC CTGGGAAGGT CTGCAGGCCA GCCACACCCT 1200
GGATAGCAAA GCATCAAAAT ACGGGAGGTA AAAAGACACA GGTAATATGT GAGACAACGC 1260
GGATGCTTGA GAAAGGGAAA CCTTGACTGA CTTGTCATGG CCTAGCTAAG AAGGAAATCT 1320
TCATGCATGC CCAGGAGGCT TTTTGCAATA AGGACTGCAC AAAGAATATG 1370
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