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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS121-00138
Organism
Homo sapiens
Tissue/cell
LNCaP
Coordinate
chr1:1270060-1270650
Target genes
Number: 49
Name
Ensembl ID
NOC2L
ENSG00000188976
SAMD11
ENSG00000187634
RP11
ENSG00000230699
PLEKHN1
ENSG00000187583
C1orf170
ENSG00000187642
HES4
ENSG00000188290
ISG15
ENSG00000187608
AGRN
ENSG00000188157
KLHL17
ENSG00000187961
RNF223
ENSG00000237330
C1orf159
ENSG00000131591
TTLL10
ENSG00000162571
TNFRSF18
ENSG00000186891
SDF4
ENSG00000078808
B3GALT6
ENSG00000176022
FAM132A
ENSG00000184163
RP5
ENSG00000260179
UBE2J2
ENSG00000160087
SCNN1D
ENSG00000162572
PUSL1
ENSG00000169972
ACAP3
ENSG00000131584
CPSF3L
ENSG00000127054
GLTPD1
ENSG00000224051
TAS1R3
ENSG00000169962
DVL1
ENSG00000107404
MXRA8
ENSG00000162576
AURKAIP1
ENSG00000175756
CCNL2
ENSG00000221978
RP4
ENSG00000224870
MRPL20
ENSG00000242485
ANKRD65
ENSG00000235098
TMEM88B
ENSG00000205116
VWA1
ENSG00000179403
ATAD3C
ENSG00000215915
ATAD3B
ENSG00000160072
ATAD3A
ENSG00000197785
TMEM240
ENSG00000205090
AL645728.2
ENSG00000215791
SSU72
ENSG00000160075
AL645728.1
ENSG00000215014
C1orf233
ENSG00000228594
MIB2
ENSG00000197530
CDK11B
ENSG00000248333
SLC35E2B
ENSG00000189339
MMP23A
ENSG00000215914
CDK11A
ENSG00000008128
RP1
ENSG00000227775
SLC35E2
ENSG00000215790
GNB1
ENSG00000078369
TF binding sites/motifs
Number: 3
TF
JASPAR ID
Coordinate
Motif Sequence
Strand
-Log10(p-value)
REST
MA0138.2
chr1:1270391-1270412
ACCAGTACCAGGGACAGAGCC
+
7.58
REST
MA0138.2
chr1:1270471-1270492
GCCAGCACCATGGACAGAAAA
+
7.69
REST
MA0138.2
chr1:1270432-1270453
TCCAGCACCACGGCCAGCACC
+
8.78
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr1
1270348
1270570
Enhancer Sequence
TGTGCCCAGA CCAGGCCTGC CCAGGTAACC CAGACCCACT GTTCTGGAAA GAGGCCCGGA 60
GGGCTCCCAG GGTACCCGCA ACCCACACCG TGAGCTCAGG AAAAGGACGC AGGGAGGCCC 120
CGGCCAGATG GCTGGAAGCC CAAATCAGGC CCTGCCGACC TGACCATGTC CCACCAGGGC 180
CCCCATCCTG CACCCTGCCA GGCACCACAG CAGTGGGAGG CCAGGTGGGG GCACACAGGC 240
ATATGCCCAG GGCAGAGCCC GCCGAGGTAG GGGTGGCACC CAGCTTCCTA CTCTGCCCTT 300
TGCCCAGTGG GTAGACAGCA TCATGACTGT CACCAGTACC AGGGACAGAG CCCAGGTGGG 360
GTGGGGGCGG GGTCCAGCAC CACGGCCAGC ACCGACCACC AGGACCCCGG AGCCAGCACC 420
ATGGACAGAA AACTGCCCAC CAGGATCTGA CGCCAGCACG CCGCCAGGCC CACACAGGGT 480
CTCCGGTCAG AGTCCCAGGG TCAGCTCCCA GCAGGGCCTA GGGGAGGCTG GACCAGCTCC 540
CTGTGCCTCA TTCCAAGGCA GCCCAGCCGG AGAGAAGGGG CACAGGCCAC 590