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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS101-00424
Organism
Homo sapiens
Tissue/cell
HT29
Coordinate
chr1:16417290-16418720
Target genes
Number: 27
Name
Ensembl ID
C1orf195
ENSG00000204464
RP1
ENSG00000215720
CASP9
ENSG00000132906
DNAJC16
ENSG00000116138
AGMAT
ENSG00000116771
CHCHD2P6
ENSG00000235084
DDI2
ENSG00000197312
RSC1A1
ENSG00000215695
PLEKHM2
ENSG00000116786
RP11
ENSG00000237938
FBLIM1
ENSG00000162458
SPEN
ENSG00000065526
EPHA2
ENSG00000142627
ARHGEF19
ENSG00000142632
ANO7L1
ENSG00000237276
RSG1
ENSG00000132881
FBXO42
ENSG00000037637
C1orf144
ENSG00000055070
SPATA21
ENSG00000187144
NECAP2
ENSG00000157191
RP4
ENSG00000226029
CROCCP3
ENSG00000080947
RP5
ENSG00000233421
NBPF1
ENSG00000219481
CROCCP2
ENSG00000215908
EIF1AP1
ENSG00000236698
ESPNP
ENSG00000116219
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr1
16417756
16418103
Enhancer Sequence
GTGTGGGTAG GTGGGTGCAG GCTCCACATG CTCTTCACTT GGCAAGAGGG AGAGGGGACC 60
TACCCCCTTC CTCCATCTGT CCTGGCCTCT CTTCCACCTC CCAACCCCAC CAAAGGCAGG 120
TCCTGCAAGG AAGCATCCCT TTCTGACTCC AGAACTCCTC CGTGGGCTGC AATGACTCTC 180
TTGGGTCTAA CCTGAGTCCT TCCTACTTTG GGTACAGACT GCTTCCTCTC CACCTGCCTG 240
CTGGGCTGGC AGATGGCAGC CACCTCTATC AAGACCCCCA ACGCTTCAGT GATGTGGAAA 300
AGAGGGGTCA CCAACCCCTC TTGCAGGGCA TCATCCTTTC TGGGCCAGGG GTGCCCTAAA 360
TCTCTGCCAG CCTCCCCTGC AAAAGGAACT GCAGCTCCTC ACACTCCAGG GCTGCTGTGG 420
GCACGTGAGG GAAATCAGGC AGAGAGGAAA TCAGACATCG GGTTCTAAGC AAAGACCTGC 480
AGTCGTCCTC TTCTGGTCAC CCCTTCAGTC TCGTGCCCTG TCCCAGCGGA GCCAGAACCT 540
TGAATGCCAA CTGGGCCAGG CAGGAACAGC CAGCCTCTCC TGGCACACCT GGCCAGGTGA 600
GCAGGTGATG AAGCCAAGAG CCAGCTCATC ACTTGGGTGT AAACAACTGC CCAGTGGGAG 660
GTTGGCAGCC ACCTCCTCTG CTCTATCCCC AGTCCCTGCC CCGTGAGCCC CGCCTACCCA 720
GAGAAAGAGG GTGTCCCAAC TTGTTGGAGG AGTTTCCATC CCACATCGGT GCCTGGTGCC 780
TGTACTGGGT GTGTGTGGGG GACTCTGATG GGGGCCCACA ACGGATCTTT GTCCTCCAGA 840
CCTGCGCCCC TCACTGTCCG GGAGGTGCCC AGCTCTTTGG AATGCCAAGG CCCCTGTCTC 900
ACCCACCCAC CCCAGATGGC TTTGCCATTC CCTCCCAGGG CCCTCGCCAG CACAACAGAG 960
CAAGGGCCGT CTGGGAACTA GGTCGTGCCT TAAGCGGAGG GAGCTTGGCT CTCTCTACCC 1020
ACCAGCTGAG AGCTGTGTCC CTTGGAAGAA GGCGTGCAGT TCCAGGTTTC CAGAAGGAGG 1080
ACGAAAACAG ACCTCCACTG AGCACTTGGC CCCGATGCCC TGCATTTGAC AGATGTTGCC 1140
TGGAAGACAG ATACTGCCAC CCTCACTTTA AAGATGGAGA AACTGAGGCA AGACCACCAA 1200
TTCCATGAAG GCTGGGACCT TCTCTGCCTT GTTTGCTCCC GGCACACAGC AAGATCTCAA 1260
GGTGTACTTG TGGAAGGGAT GAATGGGGTT CGGAGAGGGC AAGTGACGTG GCCAAGGTCA 1320
CACAGCCAGA AAGGAGCTCA ACTGGGGATA ATTCAGGCCG GTTTGAACCC TAAACTCAGG 1380
CTGCTTCTGA GACCCACCCA CCGAGGTGGA GGCATCACAC CTGCCCACAT 1430