EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS007-10889 
Organism
Homo sapiens 
Tissue/cell
BE2C 
Coordinate
chr22:41797690-41798800 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HNF4GMA0484.1chr22:41798536-41798551ACGGGGCAAAGGTCA+6.06
NR2C2MA0504.1chr22:41798536-41798551ACGGGGCAAAGGTCA+6.58
Nr2f6MA0677.1chr22:41798537-41798551CGGGGCAAAGGTCA+6.27
RxraMA0512.2chr22:41798537-41798551CGGGGCAAAGGTCA+6.2
ZNF263MA0528.1chr22:41798028-41798049TTCTCCTTCCCCTCCACCCCA-6.01
ZNF263MA0528.1chr22:41798025-41798046CCCTTCTCCTTCCCCTCCACC-7.53
Number of super-enhancer constituents: 25             
IDCoordinateTissue/cell
SE_01372chr22:41797587-41798792Adrenal_Gland
SE_03173chr22:41797596-41798927Brain_Angular_Gyrus
SE_03911chr22:41796878-41800879Brain_Anterior_Caudate
SE_05807chr22:41796662-41801176Brain_Hippocampus_Middle
SE_06715chr22:41796766-41801019Brain_Hippocampus_Middle_150
SE_07758chr22:41796906-41801025Brain_Inferior_Temporal_Lobe
SE_08854chr22:41797812-41798107Brain_Mid_Frontal_Lobe
SE_08854chr22:41798201-41798804Brain_Mid_Frontal_Lobe
SE_23356chr22:41797656-41798859Colon_Crypt_1
SE_24194chr22:41797716-41798820Colon_Crypt_2
SE_26920chr22:41797675-41798779Esophagus
SE_31944chr22:41797585-41798926Gastric
SE_40631chr22:41797035-41799308Left_Ventricle
SE_41678chr22:41797746-41798755LNCaP
SE_42253chr22:41797639-41799027Lung
SE_46916chr22:41797713-41798745Ovary
SE_47751chr22:41797625-41798846Pancreas
SE_48064chr22:41797599-41799426Psoas_Muscle
SE_48843chr22:41797611-41798932Right_Atrium
SE_49547chr22:41797699-41798891Right_Ventricle
SE_50431chr22:41797601-41798953Sigmoid_Colon
SE_51256chr22:41797373-41799190Skeletal_Muscle
SE_52989chr22:41797572-41798943Small_Intestine
SE_54774chr22:41797122-41800845Stomach_Smooth_Muscle
SE_65292chr22:41796915-41800558Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr224179811641798195
Number: 1             
IDChromosomeStartEnd
GH22I041401chr224179749141799127
Enhancer Sequence
ACTCCATCTC AAAAAAAAAA AAACAAAAGC AAAAACGAAC ACCAGCTTCA TAAGACAGTT 60
GTCCCACGAA GACACCTGGA GCAGGGCAAA CACCACTCAG CAGCTGCCAT TATGGTGACA 120
GAGAGGAAGG TACGGACCTA CATGGAGACC ATCACCTCCA GTCCCAGCAG CTGCTGCCCA 180
TCGCGGGTTG TCTACCAGCT GGTGTGGGAT GCAGCCAGGG TCAGACCAGC TGTGTGGTCT 240
TGGACAACTT ATCCATTTCC CTGAGCTGTT TCTCTCTCTG TCCAACAAGG ATGCGCTACA 300
CAGGTCACAT GTGCGTGCCT GACAGCACAT CTCGACCCTT CTCCTTCCCC TCCACCCCAG 360
CTCCTTCAAG GACAAATTCC GAAGCTGGAC ACATGCCCCC TTCCTTTACT GCACCCTATT 420
ACCAGACAGC CCTTCACACA CTGCCCCGTG GCTGTGCCAG GCTGGCCCAG CTGGCAGCTC 480
CTGACGTCAG CAGCTAATCC GGGAAAGCTG CCAGCCAGAG ATAGGGGTGA GCAGCAAAGG 540
AAATCAGAAA CAGGTTTTAA GATGGGTGCC CCAACCCCCC AGCCAGCCCT CAGGGAGCTT 600
TCATCAGCCT CTCACTTAAG CAAATCCTCG CAACCATGCG TCCTGATGCC CGGTCCCCTC 660
AGGATTAAGT AAGTGCTGAG CAGGAGGCTT TTATTTTAAG CTGCAGCTCT GTCATCAGGA 720
GCTAGGCACA CAGCAAGCCA CTGCCTAGCT GTCCCATAGG TTTCTCCAAA CAGAGTAGTG 780
GGCGTCCACT CAGGTCTGGA TTTCAGGCTG ACTCCAGGAA GTCCAGACTA CAGGGAGGTA 840
GAGGGGACGG GGCAAAGGTC AAGGATCAGA GGTAGAGGGG ACAGGACAAG GGCCTCAGTG 900
TGTTGCCTCC AGCTGGCCCT CCCTCTTAAG GCACAAGGCC CGGTGCACCA TTCCTCACTG 960
TTCTTATGTC TTCCCAGCGT ACAGCACGCA GGACGGTGCT ATGGTTTGAA TGTCTCCCCA 1020
GAATATATGG GTTGGAAACT TAATCCCTAA TGCAATAGTG TTGGGAGGTG GGTCTTAATG 1080
GAAGGTGTTT ACATCGTAAG GCCTCCACCC 1110