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EnhancerAtlas 2.0
Tag
Content
EnhancerAtlas ID
HS018-04771
Organism
Homo sapiens
Tissue/cell
CD19+
Coordinate
chr12:6921340-6922400
Target genes
Number: 53
Name
Ensembl ID
SCNN1A
ENSG00000111319
RP1
ENSG00000213942
CD27
ENSG00000139193
LOC678655
ENSG00000215039
TAPBPL
ENSG00000139192
VAMP1
ENSG00000139190
NCAPD2
ENSG00000010292
MRPL51
ENSG00000111639
SCARNA10
ENSG00000256329
GAPDH
ENSG00000111640
NOP2
ENSG00000111641
SCARNA11
ENSG00000247853
CHD4
ENSG00000111642
LPAR5
ENSG00000184574
ACRBP
ENSG00000111644
ING4
ENSG00000111653
ZNF384
ENSG00000126746
C12orf53
ENSG00000139200
COPS7A
ENSG00000111652
PTMS
ENSG00000159335
MLF2
ENSG00000089693
CD4
ENSG00000010610
GPR162
ENSG00000250510
U47924.11
ENSG00000256010
LEPREL2
ENSG00000110811
GNB3
ENSG00000111664
U47924.25
ENSG00000237240
CDCA3
ENSG00000111665
USP5
ENSG00000111667
TPI1
ENSG00000111669
RPL13P5
ENSG00000240370
LRRC23
ENSG00000010626
DSTNP2
ENSG00000248593
SPSB2
ENSG00000111671
ENO2
ENSG00000111674
ATN1
ENSG00000111676
C12orf57
ENSG00000111678
PTPN6
ENSG00000111679
SCARNA12
ENSG00000238795
EMG1
ENSG00000126749
PHB2
ENSG00000215021
U47924.19
ENSG00000255896
C1S
ENSG00000182326
LPCAT3
ENSG00000111684
RP3
ENSG00000239701
C1R
ENSG00000159403
ABC12
ENSG00000205885
C1RL
ENSG00000139178
U6
ENSG00000200345
RBP5
ENSG00000139194
CLSTN3
ENSG00000139182
RP11
ENSG00000256967
PEX5
ENSG00000139197
TF binding sites/motifs
Number: 2
TF
JASPAR ID
Coordinate
Motif Sequence
Strand
-Log10(p-value)
Foxd3
MA0041.1
chr12:6921537-6921549
AAACAAACAAAC
-
6.32
RREB1
MA0073.1
chr12:6921961-6921981
TGTGTGTGTGTGTTTTGGGA
-
6.29
HEDD
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1
Chromosome
Start
End
chr12
6921881
6922083
Enhancer Sequence
GGGTTGCTTG AGGTCAGGAG TTCGAGATCA GCCTGGGCAA CATGGCAAAA CTTGTATCTA 60
CTAAAAATAC AAAAATTAGC CAGATGTGGT GGTGTACACC TGTAATCCCA GCTACTCCGA 120
AGGCTGAGGC AAGAGAATCC CTTGAACTCA GGAGGCAGAG GTTACAATGA GCAGAGATCG 180
AACACTCGAC TCCATAAAAA CAAACAAACA AAAAAAGAAA GCAGGCTGGG TGTGGTGGCT 240
CACGCCTGTA ACCCCAGCAC TTCGGGAGGC CAAGGCGAGC GGATCACCTG AGGTTGGGCA 300
TTCGAGACCA GCCTGACCAA CAAGGAGAAA CCCTGTCTCT ACTGAAAATA CAAAATTAGC 360
CGGGCTTGGT TGCGCATGCC TGTAATCTCA GCTACTCGGG AGGCAGAGGC AAGATAATTG 420
CTTGAACCCG GGAGGCGGAG GTTGCGGTGA GCCAAGATCA TGCCATTGCA CTCCAACCTG 480
GGCAACAATA GCGAAACTCC ATCTCAAAAA AAAAAAAGCA AAGGGCATAT AGTGAAAAGC 540
TTTCTTCCTA CACATGAGTA TTCACTTCCT CTTCCTAGAG GCAACCAAGG TTATTTTTGT 600
GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT GTGTTTTGGG ACAGTCTCAC TCTCTCACCA 660
AGGCTGGAAT GCAGTGGTGC GATCTCACTG CAAACTCTGC CTCCCAGTCT CAAGCGATCT 720
TGTGCCTCAG CCTCCCAGTT TTTTTTTCTT TTAAATGGGG TCTCATTCTG TCGCCCAGGG 780
TGGAGTGCAG TGGCATGATC ATAGCTCACT GCAGCCTCGA CCTCCTGGGT CAGGTTATCC 840
TCCCACCTCA GCCTCCGGCA TAGCTGGGGC TACTGGCATG CACCACCACA CTCAGTTAAT 900
TTTTTTTCTT TTTTGAGACA GAGTCTCACT CTGTCACCTA GACTGGAGTG CAGTGGTGCC 960
ATCTCATTTG TTTCACTGCA ACCTTTGACT TCTGGGCTCA AGTGATTCTC CCACCTCAGC 1020
CTCCCAAGGC GGCTAATTAA AAAAAATTTT TTTTTTTTTT 1060