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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS129-36737
Organism
Homo sapiens
Tissue/cell
MCF10A
Coordinate
chr8:146054990-146055960
Target genes
Number: 37
Name
Ensembl ID
FAM203B
ENSG00000230567
SCXA
ENSG00000188686
BOP1
ENSG00000170727
HSF1
ENSG00000185122
GS1
ENSG00000254690
DGAT1
ENSG00000185000
SLC52A2
ENSG00000185803
ADCK5
ENSG00000173137
CPSF1
ENSG00000071894
SLC39A4
ENSG00000147804
VPS28
ENSG00000160948
AC084125.4
ENSG00000232600
TONSL
ENSG00000160949
CTD
ENSG00000254578
CYHR1
ENSG00000187954
KIFC2
ENSG00000167702
PPP1R16A
ENSG00000160972
GPT
ENSG00000167701
MFSD3
ENSG00000167700
RECQL4
ENSG00000160957
LRRC14
ENSG00000160959
LRRC24
ENSG00000254402
C8orf82
ENSG00000213563
ARHGAP39
ENSG00000147799
ZNF251
ENSG00000198169
AF235103.1
ENSG00000244307
ZNF34
ENSG00000196378
RPL8
ENSG00000161016
ZNF517
ENSG00000197363
ZNF7
ENSG00000147789
COMMD5
ENSG00000170619
ZNF250
ENSG00000196150
ZNF16
ENSG00000170631
TMED10P1
ENSG00000254618
C8orf77
ENSG00000255559
ZNF252
ENSG00000196922
C8orf33
ENSG00000182307
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr8
146055258
146055624
Enhancer Sequence
TGAGGCTGCA CCTTGGGGCC CCTTCCCCTG CATCATCAGT CAGCACCCAC CCAGCCAGGC 60
CTCCATCAGA GGCTGGGGTA TGCAGGCCAA ACGCTCAGAC CCTTGTGGGC TCCACAGGGG 120
GCTTGGACTC ATGAGTGGTG TGCCAGGCTG GTTCCTAGCT TTGCCCATGT CATGGGGTTC 180
AGCCCCCAGG GAGTGGGTGG GATTCTGGGA GTTAGTAAAG CCTCTTTTTT TCCTAAGCTG 240
TTAAATTGTG AGAAATAGAA TCCAAACTTG AAATAGCTTA GACAAGAAAA GAGAAATTAT 300
TGGGTGGAGA AATCCAAGGA AAAGGTTGTG CAACGAGCAA GAGGTGGCAG CGACGCCCAC 360
ACGGCTGCTT TGCAGATGCC GTCATCCCCT TGCCCCTCCT GTCCTGCCGT TAGTCTCCTC 420
TCTGAACTCC ACCACCGCCA CAGGCAGCCA CTGCGGTGCT CTTTATGTCC ATGCCTGTGT 480
CCTCACAAGC TGTATACTGT CGTTGGATTG CAACTTGGTG AGGGGGGGTG CGTCTTAACT 540
TGGGCCTTGC TGGGCCTCTT GCCTGTGACT AAGCCCTCTG CTGCATCACA CGCCCGAGAG 600
AGTGCCTGGG CTGGGGGATC AGGAGTGGAA CTGACGCGGG CATCGTTGGT TGGCCAGGAG 660
CTTCTTGGGG TGTTGGACCA GGCCTGTCCC CCTCTGTCCC GGCTAGTCTG GCAAAGTCCA 720
GCTTTCTGTT TTGCCAGTCA GATAAGTGTA CAGTGGGAGG CTGTTGTAGT TTGAGTTTGC 780
ATTTCTCTGA TTTCTGCTGA GCTTGAGCCT ATTTTCACAC CCTCATTAGC TTGCCAGGTT 840
CTTCTGTGAA ATATCTGTTC AGGGCATTTG CCCATATTCT AGGTCCGCTG TGTCTTATTG 900
CTTTGAAGGT GTTGTTTCTT CATTCTGTCT AAGATGCCTT ACTTTGTAAA ACATGTAGTT 960
ATGTACACAT 970