EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS176-15869 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH 
Coordinate
chr17:7213120-7214330 
Target genes
Number: 54             
NameEnsembl ID
ASGR1ENSG00000141505
ACADVLENSG00000072778
DLG4ENSG00000132535
MIR324ENSG00000199053
DVL2ENSG00000004975
PHF23ENSG00000040633
GABARAPENSG00000170296
CTDENSG00000262526
C17orf81ENSG00000170291
CTDNEP1ENSG00000175826
RP1ENSG00000262302
CLDN7ENSG00000181885
SLC2A4ENSG00000181856
YBX2ENSG00000006047
EIF5AENSG00000132507
GPS2ENSG00000132522
RP11ENSG00000261915
NEURL4ENSG00000215041
AC026954.6ENSG00000224647
ACAP1ENSG00000072818
KCTD11ENSG00000213859
TMEM95ENSG00000182896
TNK1ENSG00000174292
C17orf61ENSG00000262481
PLSCR3ENSG00000187838
NLGN2ENSG00000169992
SPEM1ENSG00000181323
C17orf74ENSG00000184560
TMEM102ENSG00000181284
FGF11ENSG00000161958
CHRNB1ENSG00000170175
SLC35G6ENSG00000259224
ZBTB4ENSG00000174282
POLR2AENSG00000181222
TNFSF12ENSG00000239697
TNFSF13ENSG00000161955
SENP3ENSG00000161956
EIF4A1ENSG00000161960
SNORA48ENSG00000209582
SNORD10ENSG00000238917
SNORA67ENSG00000207152
CD68ENSG00000129226
MPDU1ENSG00000129255
AC113189.5ENSG00000233223
SOX15ENSG00000129194
SHBGENSG00000129214
FXR2ENSG00000129245
SAT2ENSG00000141504
ATP1B2ENSG00000129244
WRAP53ENSG00000141499
TP53ENSG00000141510
EFNB3ENSG00000108947
DNAH2ENSG00000183914
RPL29P2ENSG00000240480
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr17:7213427-7213448CTTGGTTTTCACTTTTTCTTT+6.23
Number of super-enhancer constituents: 4             
IDCoordinateTissue/cell
SE_17257chr17:7209743-7214537CD4p_CD225int_CD127p_Tmem
SE_20715chr17:7209393-7214108CD56
SE_22868chr17:7209551-7214688CD8_primiary
SE_53203chr17:7209516-7213541Small_Intestine
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr1772133877213692
chr1772138337213940
Enhancer Sequence
TTAGAATTTC ACCTCCGCAT CTTGCCTTCC CCATGCCTCC AGTATCTTTG GCGCTCCCAG 60
CAGCAAGCTG CCAACAGTGC TGACTTTCCT TTAACTCTGC TTTTACTGTC TGATTGTTTT 120
TGTTTAGCGC TCAGCCTTCA TACCCATTCA GACAACTACA CCTGCTCCCC AGTCTTCAGC 180
CTCTTCTGTG GTTACCCTTC TGTCCCCGCA TCATTCTCTG GCAGTCCCTC CGTTTCTCCA 240
GCTTTGTGCC AATCTCTTCA ATTCATAGGC CTTTATGCTC TAGCTATTCA GTTGCTCCTT 300
CCTTATTCTT GGTTTTCACT TTTTCTTTCT TCCCTTGAGC CGTTGTTAAG TGGTTGCTTC 360
CATCACGTTG CCCAGGGTTT CTCCAATTCT ACGCCTTCCC CTGGAGGGAC TCCTGCGTCA 420
ATTCTGAGCT TTCAGGTCAC CTTGCTGCTT CGTTCCCCAG TTCTAGCTTT CCCTTTGGAA 480
CTCTGACGCA GGATCAAACT GCCCCTACCT GCCCCATCCC ACTCTCCTTG GGTTCCTTGA 540
GCCTCCATGC TTTCATGGGT TTTAACATTC TTGCTAGCAC TTCCCTCATC ACCTCAGACT 600
TTTCCTGTCT CTTTAGAATT TCAACCTGAT TCGTTCTTGT TGAATTTCTT GTGGTGTTTT 660
TCCTTAATCA GTTTTTCCAT CTTTTGACTT GACATTGATC TTGGATTATT CTCTAGTGTC 720
TGGATCCCTC TCTGTGCTCT TCTGGCTTCC TTATTTTCTA GCTACATAGT TATTTCTGAT 780
CTCCCTGCAA GTCCTTTTCT TCAGCTCTTT CACATTTCTT AGTTTCTTAT CCTTTCCCTT 840
CTACCTTCCT TATTCCCCAG TTTCTCAGCT CCTTCTCCTG GTGTCCGGAA AACTCTTCGA 900
AACTTTTACT CAGACTCCTC CCACTCCCCT AGACTCTTAG CATCTTATCT TTTATCAAGG 960
TAACTGTCTT CTCCAAGCCT GCCATGCAGT TTTCTATTGT GCTGTCAACC CCAATCTCAA 1020
CGGTGGTTTT TTAGCCTCTG TTTTTTTTCT TTAAGAGGCT TTACTGTTTC TTGAGTTGAC 1080
TGGTTCAATT CCAACACTCC AGTCTTTGCC CCAACAATGT AATTCTGACT TCCCTCATCA 1140
GGCAAGGTCA ATTTGAGCCT TTATTTCCTC CGTTTTAGAG TTTGGTTGGG TTTCTCTTTG 1200
TGATGCATAC 1210