EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS095-26080 
Organism
Homo sapiens 
Tissue/cell
HMEC 
Coordinate
chr6:41698210-41700380 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr6:41699222-41699243CCTTGCTTTCTCTTCCTTTTT+6.23
RREB1MA0073.1chr6:41699197-41699217CCCCTAACAACCCACCCCCA+6.37
RREB1MA0073.1chr6:41699928-41699948CCCCAGACCACCACACCCCC+6.8
RREB1MA0073.1chr6:41699196-41699216ACCCCTAACAACCCACCCCC+6
TFAP2AMA0003.3chr6:41698610-41698621TGCCTCAGGCA+6.02
ZNF263MA0528.1chr6:41699230-41699251TCTCTTCCTTTTTCTTCCTCC-6.11
Number of super-enhancer constituents: 27             
IDCoordinateTissue/cell
SE_03162chr6:41695324-41702122Brain_Angular_Gyrus
SE_03890chr6:41695262-41704164Brain_Anterior_Caudate
SE_04788chr6:41694181-41704406Brain_Cingulate_Gyrus
SE_05789chr6:41694011-41704397Brain_Hippocampus_Middle
SE_06686chr6:41695028-41704295Brain_Hippocampus_Middle_150
SE_07757chr6:41694213-41702285Brain_Inferior_Temporal_Lobe
SE_08794chr6:41698649-41698904Brain_Mid_Frontal_Lobe
SE_10407chr6:41694292-41703442CD19_Primary
SE_10977chr6:41658732-41703851CD20
SE_20329chr6:41689981-41703529CD56
SE_27930chr6:41686945-41704088Fetal_Intestine
SE_28789chr6:41686934-41704233Fetal_Intestine_Large
SE_32569chr6:41697863-41703546GM12878
SE_40921chr6:41697833-41699742Left_Ventricle
SE_48161chr6:41694453-41700196Psoas_Muscle
SE_48786chr6:41698203-41699142Right_Atrium
SE_50457chr6:41694581-41700186Sigmoid_Colon
SE_51489chr6:41697833-41703765Skeletal_Muscle
SE_53720chr6:41698008-41703677Spleen
SE_58883chr6:41671378-41704020Ly3
SE_59865chr6:41670633-41703769Ly4
SE_60547chr6:41671030-41704212DHL6
SE_61043chr6:41671264-41704230HBL1
SE_61929chr6:41668086-41703943Toledo
SE_62316chr6:41671424-41703890Tonsil
SE_65465chr6:41694557-41698785Pancreatic_islets
SE_65465chr6:41698849-41703616Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr64169952541699631
Enhancer Sequence
CTTATGGGGC CAGGTGGCTC TCCCCATAAG AAAGCTGGAC AAAAGATGGG TGGCCAGACC 60
TCATTTTTCC TCCTTAAGCC CACACTTAAG AGCCAGGAAG GAAAGCTGGT GATGACCCTG 120
CCTGTTGCCT CTGCTCCTCT TGGCTCTCAC CCACGGCTTT GCCATTTCAC AGCAAAGCAT 180
TTCCTGTGGG CATGATAAGT CCCAGATCCT ACCCTATCAC TGCGATTTTA TCTCTGTCCC 240
CAATGACATC ACAGCCAAGG GGATCTGTAT CTCTGGTGCA GTGTGGAGGA GGGACAGATG 300
ATAGGAGAGC AGGGGACAGC CACAGCTAGG AGTGCATGGT CAGTGGCCAG GCCAGATGCT 360
ACCCAGGGAA ACCCAAGTGG CAGGGCAGGG GTGGTAGAGA TGCCTCAGGC ATTGCCAAGC 420
CCCCTGCACC GTCTTATTCA ACAAGGAGAG GAGGCTGGTG TGGTGGGACA GAGAGTGGTG 480
GGAAGCCCCA CGTAAAGCAT TACATCAGAG AACATTAGAC ACATGGAGAG GCCTGTTTGC 540
AACCCATAGG TCTTTATTCC TTCCCTAGAG CTCTCCATGC CTCTATTTCC TCACTTAAGA 600
ATGAGAAATA AATAACTCAC TGAGTCATAA CAGTTCATTA GGCGCTATTC TAAGTACTAC 660
ATGTGCATCA ATATCGGCAT ACTCAGCCCT CACGACAGCA CTAGTAGGTG GGTGCTGCAA 720
GAACCCTCAC TTTTTAGGTG TGGAAACTGA GGCACAGTGG GGTTAAGCAG CTTGCCGAGG 780
CTCACACAGT GTTAAGTGGC AGAGCTGTGC AAGCCACATA GCCTGGCCCC AGAGCCCACG 840
TTCTCAACAA CCCCCTGACC AGGTGACACT GGTCCAGTGC TCAATATATA GTGGCTATGG 900
CTGTCCCAAG AAAAACTTCC TGGTTGCTTC ACCAGGACCA GTCTTTAGCT AAAGCTCAAT 960
TCTGCGGACT GCAGCATCTC CCAAACACCC CTAACAACCC ACCCCCACCA CCCCTTGCTT 1020
TCTCTTCCTT TTTCTTCCTC CCCGGTGCCT TTGGCAAAGA TTTGTAGAAG GTTCGCTTTG 1080
GAGGGAATCC CACAGATGAT CCAGATTCAC AGATATGGAA ACTGAGGCTG AACAAAGCAG 1140
AGACCTGCCC AGCCACACAG CCAGTGAGAG GCACAGTGGG GTCTCTCGAC TCCTGGTCCA 1200
GTGCTCTTAT GACTTTACTG CCGTCCCATT CTCACCCAAT GATCCCCACA GCCTCTTCTG 1260
CACATCTGAT TAAACAAGGG CCTGCTGAGG GCTGCACTGT ACGTTAATGG ACGTGGAATG 1320
CATGGCACAA AGCCGGGCAC CTAGAAGGCC ATCAGTAAGG ATGCCTCCTC CCTTCCTGGG 1380
TGTCTGGGGC TTCCAAAGAA GCCCAGGAAG TCTTGCCTGA ACCAGTCTCC TTCCCTGGCC 1440
AGTCAAGACA GGTTCCAGCC GGAGGTCCTT TGGTCACCCA TGCTGGCAGC TCAGAAGAAA 1500
GGCCAGGAAA CAGGTATGGT GCTCAGACAG GGGCCTCAGC AAGTTCCCAC CCTGCTTTTT 1560
TATTTTTATT TTTTTCATAC AAATTCTTTT TTCAATTGAG TCCAGGTCTC GCTATGTTGC 1620
CCAGGCTGGT CTCGAACTCC TGAGCTCCAG TGATCCTCCC ACCTAGGCCT CCCAAAGATC 1680
TGCTTAGAGC AGGAAACCCT GGATAGAGAA AAGAAGGTCC CCAGACCACC ACACCCCCAC 1740
CTTTTAAGAG AGAACTCCTG GGAAACCCCT TGAAGAAGTG GTCTTCTTTA GGGACTGAGA 1800
ACACAGACTT TGGAGTCAAT TGGACCTAGG TTAAAATTCC AATCCTGTCA CTTCCAGGCT 1860
GTGTGATTTT AAGTGACTTG CTTAACCTCT CTGAGTAAGT AAGTGTAATG CAAACAGTAA 1920
TTCCCACCTC ACTCTAAACA CACAATAAAT GTTGGCAACT ATTGTATAAT CAATCTTATT 1980
ATAATATTGT TCTAGTATAG CATAAAAGAA GAGATGAATA TTCTATTAAT ATAATCTTGT 2040
TTTATTGTTA CACTCTCATA GACACACATG CACAGTTCAT CTCTACCCAC ATTCCTAGAC 2100
ACTTTAACCA CACACACAAA CTCACAACCA TTACATAAAC CCCACACCAA CCCAGAAAGC 2160
AACATCATGT 2170