| Tag | Content |
|---|
EnhancerAtlas ID | HS108-21313 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr19:59095760-59098140 |
Target genes | | Number: 20 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| DBP | MA0639.1 | chr19:59098127-59098139 | TATTACGTAATG | - | 6.18 | | EWSR1-FLI1 | MA0149.1 | chr19:59097072-59097090 | CCCTCCCTCCCTCCCTCC | - | 6.03 | | EWSR1-FLI1 | MA0149.1 | chr19:59097065-59097083 | CCTACCTCCCTCCCTCCC | - | 6.28 | | EWSR1-FLI1 | MA0149.1 | chr19:59096992-59097010 | CTTTCCTTTCCTCTTTCC | - | 6.32 | | EWSR1-FLI1 | MA0149.1 | chr19:59097053-59097071 | CCTTCTTCCCTTCCTACC | - | 6.67 | | EWSR1-FLI1 | MA0149.1 | chr19:59097049-59097067 | CCTCCCTTCTTCCCTTCC | - | 6.68 | | EWSR1-FLI1 | MA0149.1 | chr19:59097061-59097079 | CCTTCCTACCTCCCTCCC | - | 6.89 | | EWSR1-FLI1 | MA0149.1 | chr19:59097010-59097028 | CTTTCCTTCCTTCCCTTC | - | 7.57 | | HLF | MA0043.2 | chr19:59098127-59098139 | TATTACGTAATG | - | 6.11 | | PAX5 | MA0014.3 | chr19:59096085-59096097 | ATGGTCACGCTC | - | 6.37 | | ZNF263 | MA0528.1 | chr19:59097079-59097100 | TCCCTCCCTCCCTCTTCCCCT | - | 6.11 | | ZNF263 | MA0528.1 | chr19:59097016-59097037 | TTCCTTCCCTTCCCCTCCCTC | - | 6.15 | | ZNF263 | MA0528.1 | chr19:59097056-59097077 | TCTTCCCTTCCTACCTCCCTC | - | 6.17 | | ZNF263 | MA0528.1 | chr19:59097092-59097113 | CTTCCCCTCCTCCCCTCCCCT | - | 6.17 | | ZNF263 | MA0528.1 | chr19:59097060-59097081 | CCCTTCCTACCTCCCTCCCTC | - | 6.27 | | ZNF263 | MA0528.1 | chr19:59097064-59097085 | TCCTACCTCCCTCCCTCCCTC | - | 6.46 | | ZNF263 | MA0528.1 | chr19:59097032-59097053 | CCCTCCCTCCCTCGCTCCCTC | - | 6.76 | | ZNF263 | MA0528.1 | chr19:59097068-59097089 | ACCTCCCTCCCTCCCTCCCTC | - | 6.86 | | ZNF263 | MA0528.1 | chr19:59097024-59097045 | CTTCCCCTCCCTCCCTCCCTC | - | 6.93 | | ZNF263 | MA0528.1 | chr19:59097076-59097097 | CCCTCCCTCCCTCCCTCTTCC | - | 7.26 | | ZNF263 | MA0528.1 | chr19:59097087-59097108 | TCCCTCTTCCCCTCCTCCCCT | - | 7.4 | | ZNF263 | MA0528.1 | chr19:59097020-59097041 | TTCCCTTCCCCTCCCTCCCTC | - | 7.55 | | ZNF263 | MA0528.1 | chr19:59097072-59097093 | CCCTCCCTCCCTCCCTCCCTC | - | 7.97 | | ZNF263 | MA0528.1 | chr19:59097084-59097105 | CCCTCCCTCTTCCCCTCCTCC | - | 8.97 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 59097037 | 59097242 | | chr19 | 59097268 | 59097469 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I058584 | chr19 | 59095961 | 59096110 |
|
Enhancer Sequence | TTTATTATTA CTCTTTGTTG TGTTACTAAT ATAACCTAGG AATAAACGGT GTGCTGAAGG 60
GACATTGTGA GAAGTGACCT AGAAGGCAAG AGGTGAGCCT TCTGTCACAC TCACATAAGG 120
GCTGCTTGAG GGCTCCTTGG TCAAGTGGTA ACGTTAGTGT CTGGGACAGC ACCGTTACTT 180
AGCAGACCAC AAAAGGGAGT CTCCTTTCCT TGGGGGAGTG AGGGAACACT CTGCTCCACC 240
AGCTTCTTGT GGAAGGCTGG ATATTATCTA GGCCTGCCCG CAGTCATCTG GAGGCCGAAA 300
CCCCTCCCTG TGGTGCTGTG CTTCAATGGT CACGCTCCTT GTCCACTTTC ATGCTCCTCT 360
CACACTCCTG GTTCCTCTTT GAAGTTTGTA GTAGATAGTG GTAGAAGAAA TAGTGAAAGT 420
CTTAAAGTCT TTGATCTTAT AAGTGCAGAG AAGAAATTGC TGATGTATGC TGCCTTCTCT 480
CTCTGCTTCA GCTACCTAAA AGAGAAGGGC CCCTGTCCTG TAATCACATG ACTTGCTTCA 540
CCTTGTCAAT CACTTAGAAG ATTCACCCTC CTTACCCTGC CCCCTTGTCT TGCATGCAAT 600
AAATATCAGT GAGCCCAGCT GTTCGGGGCC ACTACTGGTC TCTGCATCTT GATGGTGGTG 660
TTCCCCCAGG CCCAGCTGTT TTCTCTTTAT CTCTTCGTCT TGTGTCTTTA TTGATTACAA 720
TCTCTTGTCT CTGCACATAG GGAGAACACC CCCTAAGCCC CGTAGGGTTG GACCCTACAT 780
CTAGTTACTC AGGAGGCTGA GGCAGGAAGG TTGAAGTTGA GCCCAGGAGG TTGAGGCTGC 840
AGTGAGCCAT GATTGTGGCA CTGCACTGAA GCCTGGGTGA TAGAGTGAGA CCTTGTCTCA 900
AACAGCAACA AACAAATACC ATCTTTGGGT ATATTAATCA GATGGGGGGA GTCACACTGA 960
CATCAGTTGG CACCCACTGG TTAGTGTGTG CCAGGCAGGG AGACTGGGCT GTTTTCAGTA 1020
AACTGATCAC AGCAGTGAGC TGTGATCGTG CCACTGTACT CCAGCCTGGG TGACAGAGTG 1080
AGACCTTATT TCCAAAAAAA AGAGAAGGCA TTGGAGTTCA GCTTGTGGTT TTGACAGAGA 1140
AATAATAGGA TAAATTAATG AAACAAAAAA GTTAACAGTA GAGGATTAAT AAAACTAAGT 1200
TTTTTTTTTC TAATTTCTTT TCCTTTCCTT TCCTTTCCTT TCCTCTTTCC CTTTCCTTCC 1260
TTCCCTTCCC CTCCCTCCCT CCCTCGCTCC CTCCCTTCTT CCCTTCCTAC CTCCCTCCCT 1320
CCCTCCCTCC CTCTTCCCCT CCTCCCCTCC CCTTTGTATG TAAGTGTAGA TGAGGGTGTC 1380
TGTGCCTTGT GTTTGTATAT GTGAGTATCC ACATGAGCAT GCCTATGTGT ATGAGTGTGT 1440
ATGTGAGTGT GGTGAGTTGC TTCTGTCCAC ACATTTGTGT ATATGAGTGT GCATGCAAGT 1500
GTGCTGAGTG TGAAAGTGTG CCTGTAGACA TGTTTGCCTG TGTGTGCGTG TGTCAAACAC 1560
AGCTGTTTCT GTGTGTGAGT GTGCCTTATC TGTGTGTGTG CACGTGTGTG TGCACGTGTG 1620
CACGTGAATG TGTTGAGTGT TCCTGTGTGA ACACAGGTGT GTTCCTATGT GTGTTATGTG 1680
AGCATGTGCA TATGTGTATT CTCGAGGGCT GAGGGACCCA GCCCTACCTT CAGCACCTGC 1740
TAACTGTCCC CACACCCACA GCGGGCCCAG CACAGGGATC ACATTGTCGG GGTGACCTGG 1800
ATCCTACTTG AAGCCTTTGA GCTGGACTGT GGCTTTATCC CTGAGGCCAG GCTTCATGTC 1860
CAGATGGCCA TGCCAGAGGT TGACGTGGCA GAGAAGGAGT GTGACACAGG CCAGTGGAGC 1920
GAGTGGAGCC AGCCTGTGTG CTTCCAGGCT CCCCAGAGAC AAGGTGGGTG CTTCTGTGGC 1980
TGCTGCACTT CCAGAATCTG GGCTGGGTGT CTTCTCCCAT GATGACCTCA CTCCTCCAAC 2040
CTTTCACACT CCTGGAAGCC CCTCCCTGAG GCAGCCATGC CCCAGTTGAC TTGCTTCCTC 2100
TGAAGGTCTG AGGTCTATAG GGAGGACACA AGCTCCTGCC CTAACACATC TCTGCACACC 2160
TGGTGGTCTT AGGTTAGGGT TAGGGTCAGG GTCAGGGTCA GGGTCAGGGT CAGGGTTAGG 2220
GTTTAGGGTC AGGGTCAGGG TCAGGGTCAG GGTTAGGGTA GGGTTAGGGT TAGGGTTAGG 2280
GTTAGGGTAG GGTTAGGGTT AGGGTTAGGG TTAGGGTATT GTAAATAATT TCACATTACT 2340
AATAATAAAT TATTATTTGT ATTACACTAT TACGTAATGT 2380
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