| Tag | Content |
|---|
EnhancerAtlas ID | HS038-12651 |
Organism | Homo sapiens |
Tissue/cell | ESC_neuron |
Coordinate | chr2:237764570-237767290 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF14 | MA0740.1 | chr2:237765375-237765389 | GGGTGGGCGTGGCC | - | 6.69 | | KLF14 | MA0740.1 | chr2:237765385-237765399 | GGCCACGCCCCCTC | + | 7.52 | | KLF16 | MA0741.1 | chr2:237765386-237765397 | GCCACGCCCCC | + | 6.62 | | Klf12 | MA0742.1 | chr2:237765374-237765389 | AGGGTGGGCGTGGCC | - | 6.37 | | Klf12 | MA0742.1 | chr2:237764864-237764879 | GGGAAGGGCGTGGCC | - | 6.59 | | SP1 | MA0079.4 | chr2:237765376-237765391 | GGTGGGCGTGGCCAC | - | 6.97 | | SP1 | MA0079.4 | chr2:237765383-237765398 | GTGGCCACGCCCCCT | + | 7.04 | | SP3 | MA0746.2 | chr2:237765385-237765398 | GGCCACGCCCCCT | + | 6.82 | | SP3 | MA0746.2 | chr2:237765376-237765389 | GGTGGGCGTGGCC | - | 7.52 | | SP4 | MA0685.1 | chr2:237765374-237765391 | AGGGTGGGCGTGGCCAC | - | 6.92 | | SP4 | MA0685.1 | chr2:237765383-237765400 | GTGGCCACGCCCCCTCC | + | 7.6 | | SP8 | MA0747.1 | chr2:237765376-237765388 | GGTGGGCGTGGC | - | 6.62 | | SP8 | MA0747.1 | chr2:237765386-237765398 | GCCACGCCCCCT | + | 6.92 | | ZNF263 | MA0528.1 | chr2:237765851-237765872 | CCCTCTCTCTCTCCCGCCCCC | - | 6.14 | | ZNF263 | MA0528.1 | chr2:237765756-237765777 | TCTCCTTTTTCTCTCTCCTCT | - | 6.18 | | ZNF263 | MA0528.1 | chr2:237765743-237765764 | CCTTCTCCCTCTCTCTCCTTT | - | 6.36 | | ZNF263 | MA0528.1 | chr2:237765860-237765881 | TCTCCCGCCCCCTCCTCTTTC | - | 6.38 | | ZNF263 | MA0528.1 | chr2:237765857-237765878 | CTCTCTCCCGCCCCCTCCTCT | - | 6.58 | | ZNF263 | MA0528.1 | chr2:237765811-237765832 | CCCTCCCCTCTCTCCTCTTTC | - | 6.61 | | ZNF263 | MA0528.1 | chr2:237765733-237765754 | CTCTCTCCCTCCTTCTCCCTC | - | 6.63 | | ZNF263 | MA0528.1 | chr2:237765808-237765829 | TTTCCCTCCCCTCTCTCCTCT | - | 7.01 | | ZNF263 | MA0528.1 | chr2:237765879-237765900 | TCCTCTCCCGCCCCCTCCTCT | - | 7.15 | | ZNF263 | MA0528.1 | chr2:237765727-237765748 | TTTCCTCTCTCTCCCTCCTTC | - | 7.25 | | ZNF263 | MA0528.1 | chr2:237765730-237765751 | CCTCTCTCTCCCTCCTTCTCC | - | 7.25 |
|
| | 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 |
| GH02I236855 | chr2 | 237763973 | 237766684 |
|
Enhancer Sequence | TTGGTGGGTT ACGATTTTGT TGACCACACC ATGTGCATCC ACACTTCTTC ATTCTCATGA 60
GTAGCTCTTA TTGGAATGTG AGCTCCCTGG GGCAGAGCCC GTGTCCCGCT CACCTTTGCA 120
ACCCTCTCAC CTGCCACTGG ATCTCACACA CACAGTGGAA GCATCATAGG TTTCAGATAA 180
ACTGAGTTCA GCCGTCTCCC CTACTCCCCT AAATTGCATT TCTACTATCC CTGCTAACAT 240
CCTAATGCTT CACTTCAAAG AGCAGAGCAG AGCAGAGAGC TTTAGACACT GCCTGGGAAG 300
GGCGTGGCCA CGCTCACCTT GCACACATCA ATCTTCAGAC GACCGCCTCT CCTACCCTAG 360
GGTGATGCAT ATTTGAATGG GAACTCCTGG AGACCAGAAT CCCTGAGGCT TGGAGGAGTG 420
ACAGTTTGAA GGTGGAATGA CAGGTTGCAG GACGGACTTT CTCAGGCACT TCTTCCCCGC 480
ACTGTCTGCT TGGGCGGGGC AGGAGCCTGG GTTAAACCAC TCTCACCTGA GCAGGACCCA 540
GACTGGCAAT TTTATTTTCT AATATCTACG CCAATGCCTG GCTGCCTCCT GGTCTGTAAG 600
ACAGACAGAC CAAGCCATCT GAGGACAGAA AGGCAGGGTG GGGCTTAGAG GCTGGATCTG 660
GGGCACCTGG ACAAACTGCC CTTGCCAGCA GTGTCCCCTC CGCTGGTGTC CGATGTGGGC 720
TCCATCGTGG CTCAGGCTTC CATGTGCATC TCCAAAGCAC ACCTTCCTCT CCAGCAGGAT 780
CACTTTTACG GCTCCCACGT GGACAGGGTG GGCGTGGCCA CGCCCCCTCC CCAGGCAGTG 840
TCTAGAGCTC TCTGCTCCGC TGTGCTCTTT GGTCTGTCTC TGGGTTGGGG CCAGCCAGTT 900
TGAACCTCAA CAAAGGCAGG ATTTAAAAAA AAAAAACAAA AAAAAAAACA ACAAAAAAAC 960
ATGCTCCATG CTTAGAGAGA ATGAGATTTT AGACCTGTAA TTGAAAAATG CCTAGGGGAA 1020
GAGTACCTAA ATGGAACCAC CAATAACACA GGAAATTGAT TCTCTGCAGT TTTACAGACC 1080
AGCCGGGACC GCTGATGACA AGCCTCCTCC AAGCCAAACC CAGCAGTGCA GGCACTGAGG 1140
CCTTCTCCCT CTCTCTCTTT CCTCTCTCTC CCTCCTTCTC CCTCTCTCTC CTTTTTCTCT 1200
CTCCTCTAGA GACAGTCTCT TCCTCTTTCT CTCTTCTCTT TCCCTCCCCT CTCTCCTCTT 1260
TCCCCTGTCT CCTCTCTGTC TCCCTCTCTC TCTCCCGCCC CCTCCTCTTT CCTCTCCCGC 1320
CCCCTCCTCT TAACTCTCCC GCCCCCACTC TCTGGGGCTG GGTTAGCTAT CTGTGAGGCT 1380
CCCAGAGCTG GAGGCACCGA GCCCACCCTT CTCCTAGACA AAGCAGCACA CAGGCAAACT 1440
GGAGTCTGTA ATTAGATGTC TTCCAGGGCC CTCCTGCCGG GCTCCTTTCA GCAAAGTTGC 1500
GACCCCTCCC GCTGGCCCTC TTCAGATTGC AGACCATCTT CTGACCACGC AGGGAGTCTG 1560
CAAGGCCTCA AGTTGCAGCT TCTCTGAGCT GCTCAGAGTT GCTCTGAAGG AAAGCAGACG 1620
ACACCAGCCT CAAAACGGTG GCCACTCTGC CGGGCCCAGT TCAACACAAG TGCTGGCCTC 1680
TGAAGTCAGA ACCGACCCAG CTTGAGTCTG GCTGCAGGGG GCAGTTGCTC AGCCTCCCTC 1740
ATCTGTGCTA GATCAGGGGT CGGGGTGTAA ATATTTTTGG CCATAAGGTC TCAATGGCCA 1800
CTACTCAGCT CACCCACAGC AGAGCAAAAG CAGCCCTAGT CAATACGTAA ACAAATGAGC 1860
ATAGCTGGGT TCCCAAAAAA CTTCATTCAC AAAATCAAGT GGCAGCAGGA TTTGGCCCAG 1920
GGTGGCAGTC TGCTGAGGAT CATGAGGGTG CCTATCATAT AGGAATGTTG AGAAAACCTG 1980
AAACGCCTGT TGGGCTCTTT GTAGCGCAGA AACACAGCCA GGAAACGCTG ATTAATGCAT 2040
GTGCATGGCA CCCAAGCCTT GGTTCAGGGT CAGGACTGGT CCTGCATGGA GTCTGCTGTA 2100
GAACACAGGA TTCGCCTTTG ACCTCTCCAG GCTGCTGCAT ATGGAAAATG GGACGGTGAA 2160
ATTGAATTCG CGTTGATGGT TCACAAATGT CAGATGCATC CACACCCTAA CTGAGCAAAT 2220
GACTCCTACA CACTTTGACA CACCTAGCCC TGGTGGTGGA CACCCGGAGG CTGCAGCAAG 2280
AGGGGAGGTC CTGTTGATGC TATCACTAAA TATTTCTAGA CTCTGCCTTT CTGTTCTGTA 2340
ACTTTGCATC TTCACAGTCA CTGTGTCATT TCCCGTCTGC ATCACGGATT CTGCCTCTCA 2400
CCCTATCCAC TGCAACCTTT CCTCTCCAGG CTGCCAGGCT GTTCTTTTGA CAATGCAAGT 2460
CTGATGGTGT CAGCTCCTGT CTAAGATACT CAATGGCTTC TGCAAAATTC CACAAAGCCC 2520
TTCTAGTAAG GGGTTTATGA GCTGCTTTAG CTCATCAGCC CTTCACTGGA GGCATAATGG 2580
GCTGGAAGGG TGAACATGGA AACACTAGCT GATTATCTCT GTGGGGGATT TGGTGAAGAC 2640
AAAAGGGGAG GGGGACTACA CACACTTCTT ATTTTATATG CATTTGTATT TCTTGAATTT 2700
GTAAATTATG TATTCGTTTT 2720
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