| Tag | Content |
|---|
EnhancerAtlas ID | HS048-12152 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr14:100412530-100414490 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr14:100413389-100413408 | GTGCGCCACCTGGTGGCAG | - | 7.31 | | JUN | MA0488.1 | chr14:100412537-100412550 | ATGACATCATCAC | - | 6.87 | | JUND(var.2) | MA0492.1 | chr14:100412536-100412551 | CATGACATCATCACA | - | 6.5 | | KLF5 | MA0599.1 | chr14:100413101-100413111 | GGGGCGGGGC | - | 6.02 | | RREB1 | MA0073.1 | chr14:100413458-100413478 | TGGGGAGGGTTGGGGTGTGG | - | 6 |
|
| | 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 |
| GH14I099946 | chr14 | 100412938 | 100413552 |
|
Enhancer Sequence | GGACACCATG ACATCATCAC AGCTGACAAA CTTGATGATT TCAGTTTCTC GGGCTGTCAA 60
GCCTGATGCT GTGTCTCAGA GCCTGGCTGC ACAGGAGCCT AGAACAGCTG CCTGGCCTCC 120
CTGCTGAGCA GTTCAGGGTC GGGTGTCGAG CGTGCAGCCC CCAGTTCTGA ACCCTTCTCC 180
AGAGCCCAAT TCTTCCCCCC TGACCCCGCT GCTCGATGCC TAGTGGCATC CCTGCCCCTC 240
CCCATCTCCT GCAGACGGGA TGCTCAGTGC TGTCTGAAAC CTGGGCTCCT TCCATCTCCT 300
GCCGGATCCC TGGCTGTGCT TTAGGCCACC TCAGGAGACC CCCTTCTGGG CCAGACAGCC 360
TGGATCTTCC CTACCTTGCT GGCAAGCCAG ACCGGACCAC AGAAGCCTTT CGGAGTACCA 420
AGTTCCCTCT TGAAGGAAGG AGGCTTGTTT AAGGGGAGCC TCCCCTGCAG GAAGTCCGTG 480
CCCTCCTGGG GCGTTCCAGG GGGTCCGCAG GTCAACTCTA AGTTTCAATA AAAATGGGGC 540
ACACGCGCAC ACCACCCTGC GCTAGGGAGC TGGGGCGGGG CTGCGGGTAG CACACACTTT 600
CTCGCTGACT GCCCCGGATC TCAGGGGACC CCGGCGTGCG GGAAGCCGGA GGGGACGTGA 660
GATTCAGGGG CTCTGGAACA CAGGTGACGC CTGGGCTTAT AATGCGGGCC AGTTAAGAAC 720
AAATTTGGCT ATTTAGGCTG AAAACACGAG TAGCTGCTCT AGCAGACTGA ATAAGTAATT 780
ATGAAAAGAC CTTGAACTTG GGTTATAAAT TGAAAACCTC CCCTTCCCAA GCCCCCTCCA 840
GCCCCGCGGC CAACTGCAGG TGCGCCACCT GGTGGCAGAA GAGCAGAGCA CCGCCCCTCT 900
CTCCAGCTTG CCAGGGCTGA TTCTGACCTG GGGAGGGTTG GGGTGTGGAG AGAGAAAGGG 960
AAACTCTAGT TGACTTTCTG GGTGGGGCGT ATGTTTCAAC TGACCTTCTG AGAGAGCTTT 1020
CAGAGGTTCT TGGAGAACCC CAACGTTGCT GATCGCCTCT CAGCTGCAGT CCCCTGGACC 1080
TGAATGAAGG TGTTCTGTTT AGGTGCGGCC TCCTTCTGCA GCCCTGAAGC ACCGGGAGGG 1140
CTGCCTCCAT CGGCCTCCTT CCTGCGGAGA TCCCACCGCC CTCCGGGGAA GCCCGCTAGA 1200
CAGGATCTTA GACGACCTTG CTTGGATCCT TGCTTGGAGG TTCACATCTG GTCTCAGGGG 1260
ACACTTGTGC CTCCCACACC CACACCTTGC ACCAGTGGGT GGGCAGTTAC TGCCTTCCAC 1320
ATGCAGCCTT CTCTGGGCAG CTGGCGCTTT TGAGGCACTG GTCCACAAAT CGCAGATGGC 1380
ACACCTCAAG CCCTCCAAGT GGCTTAGGCA GAAGTACCCT CCCTGGTCCT CCCTCAGGAG 1440
AAGCAGGGTT GGAATCAGCA GCTCAACTTT CTCCCAAAGA AATCCTCCTT GCAAATATTA 1500
CTTCTGAAAA TGTCTAATTC CCAACGCTTT AGTACTCTTA TCGTGGATGA GGATGCCCAG 1560
GAGGTGTCTC GGGAACCTCT TTTGTAACTG CTGCTCATGG TCTAACAGTG CCTCTGGAAG 1620
ACACATCTAT TGGATCTTGG CTCCTCGGCT GAACGCTCAT TTCAACATCC AGTTACATAA 1680
CCACAAACAT TATTGCACAA GTTTTTTGTA CATGTTTGCA AGAAATTATC TGGGATCCTA 1740
CCTGGAAATG GGACTACTGA TTTTCTGGGG CATGCATTAA ATATTGCCAA ACCATTCTCC 1800
ACAGCAGCTC CACTGGCAGC CTGGGAGTCT CTGTTGCTCC ACTTCCTCAT CCATATTAGG 1860
AATTGTCATT TCATCTCATC TCATACAGAC CCGAGAAGCA GGATCCATCG CCCCTCTTTG 1920
AAGAGAAGAA AGAGGGTATA TTAGGCTGTT CTTAAACTGC 1960
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