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

TagContent
EnhancerAtlas ID
HS078-02016 
Organism
Homo sapiens 
Tissue/cell
H2171 
Coordinate
chr1:226909350-226912520 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxd3MA0041.1chr1:226911530-226911542GATTGTTTTTTT+6.44
IRF1MA0050.2chr1:226909507-226909528CTTTTCTTTCTTTTTTTTTTT+6.41
Number of super-enhancer constituents: 32             
IDCoordinateTissue/cell
SE_00103chr1:226910268-226914123Adipose_Nuclei
SE_03869chr1:226909642-226914235Brain_Anterior_Caudate
SE_04801chr1:226909769-226913572Brain_Cingulate_Gyrus
SE_05781chr1:226909371-226914464Brain_Hippocampus_Middle
SE_06710chr1:226909842-226916981Brain_Hippocampus_Middle_150
SE_07746chr1:226909997-226913021Brain_Inferior_Temporal_Lobe
SE_10887chr1:226909951-226923692CD20
SE_11833chr1:226909764-226911682CD3
SE_14432chr1:226909851-226912708CD4_Memory_Primary_7pool
SE_16856chr1:226911061-226912520CD4p_CD225int_CD127p_Tmem
SE_17296chr1:226909602-226929357CD4p_CD25-_CD45RAp_Naive
SE_17765chr1:226909495-226928628CD4p_CD25-_CD45ROp_Memory
SE_18263chr1:226909481-226929370CD4p_CD25-_Il17-_PMAstim_Th
SE_19160chr1:226909740-226917128CD4p_CD25-_Il17p_PMAstim_Th17
SE_20012chr1:226910259-226912653CD56
SE_21455chr1:226909788-226913136CD8_Naive_7pool
SE_21910chr1:226909778-226912096CD8_Naive_8pool
SE_22315chr1:226909647-226920088CD8_primiary
SE_25774chr1:226910377-226912751Duodenum_Smooth_Muscle
SE_26570chr1:226910465-226912445Esophagus
SE_31634chr1:226911457-226912281Gastric
SE_40782chr1:226909759-226913910Left_Ventricle
SE_42228chr1:226911370-226913154Lung
SE_48643chr1:226911574-226912796Right_Atrium
SE_50140chr1:226909756-226911426Sigmoid_Colon
SE_53341chr1:226910761-226911343Spleen
SE_54498chr1:226909687-226917100Stomach_Smooth_Muscle
SE_55112chr1:226910349-226911054Thymus
SE_58303chr1:226819953-226937809Ly1
SE_59629chr1:226819233-226928465Ly4
SE_60416chr1:226819368-226929640DHL6
SE_62233chr1:226813614-226929647Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr1226911425226911742
chr1226909849226909917
Number: 1             
IDChromosomeStartEnd
GH01I226722chr1226910218226912514
Enhancer Sequence
CACGCCTGGC TAATATTTTG TATTTAGTAG AGACGGGGTT TCACCATGTT GGTCAGGGTG 60
GTCTGGAACT CCTGACCTCA GGTGATCCAC CTGCCTCAGC CTCCCAAAGT GCTGGGATTA 120
CAGGCGTGAG CCACCGCACC TGGCCTTTTT TTCTTTTCTT TTCTTTCTTT TTTTTTTTCT 180
TGAGATGGAG TTTTGTTCTT GTGGCCCAGG CTGGAGTGCA GTGGCACAAT CTGGGCTCAT 240
TGCAACTCCC GCCTCCCGGG TTCAAGCGAT TCTCCTGCCT CAGCCTCAGG ATTAGCTGGG 300
ATTACAGGCG CGCACCACCA CACCCAGCTG ATTTTGTATT TTTAGTAGAT ACGGGATTTC 360
ACCATGTTGG CCAGGCTGGA ATCGAACTCC TGACCTCAGG TAATCCACCC ACCTCAGCCT 420
CTCAAAGTGC TGGGGTTATA GTCATGAGCC ACCGCACCCA GCCATAAACT ATTTTCTGAA 480
GTTGCTCAAG TCTTCTTTGC AAAGTCAGTG TTCCCAAACT ACAGTCAGAG GCCAGGCTCA 540
AGGTTCCTAG CAACCTGCCA CCTGGTACAT TCAGGGCACT CGCCCTTCAA GCACAACATG 600
GATCCTTGGG GCTCCTTGCC ACTCCAACTC CTAGGAGACT CTCCTGCCTT CCCCTGGGAA 660
TGTGGTATTT GAGGCCAATG GTGACTGACC AGAAAATCTA GGCCAGTTCA AAATGCCAAA 720
GACAGGATGC CAGGAAGGAC CCAGAACCTG CAGGGCTCCG TTCAGCTTCT TGGGGTTAAC 780
CAGCAGTCTG CAGAGGCGGG AGACGGCTCG GCTCTCAGGA GAGAGCAGCT GATTTTTAAT 840
GTACAGTGTA ATACCGCAAG GTAAACAGCA TCCCAGACGC TGCTCCATAT GGCTTTACCC 900
TGAGATCGAA ACTAATTACC ATTCTGTGTA TATTTCCAGG TTGGGGCAAT AAGGGAGTTA 960
CTGTCCAGCA CATTCGCCAT CAGACCACCC CTGAGGTCAA CACTGCCACG TGCTAACAAG 1020
CTCCTTTCGT GGTTTCAATC CTCCCAGACA TCAGTCCCTT CATCCTGCAA AGGGCAGAAA 1080
GAAACTGGGG CTTGGGGAGG TGTTAGGGCA GGCTGAGCCT GAGACACATA TGTCTAGAAA 1140
GGGGCAACGT CTCAAAACTG CACATTCAGA GCCTGGAAGC TCTGTACAGA TGCCTAATGG 1200
GTCCTGGGGC TAGAAAAGGT TTGAATAGAT CATCCTGGAC AGAAAAGATG CAAACCCCCA 1260
GGGGTCAACC CTGCAGGCTA CCTGCTCCCC CTGCCCCCCA CCCATTACAG CTGAAAGGAA 1320
GGAGAGAGTT CCATTTCACA CATCCTGTGT GTAGCAGAGT AGAGACCAGG GTTTGGCAGG 1380
CAGGATGCCC AGGGCTGTGG TGACGCCAGT CCGTGCTGCT CAGATGGAAC CTGTAGCCAT 1440
CCAGCCCGGA TCCTGCATGG GTTCCAGTAG GCCCTCCTGG GACTTGGAAG TGAGCTGGTG 1500
TGCTCGGGGT TCATCAGCTC CGTCCAGTCA CCTGACTGGC TTTTCCTTCC ACTCCACCAT 1560
CCCAGCCCAG ATGACAAGGG CACAGTATGG CCTTGTGACT TGGGAAGTCC TGGGTAGGTT 1620
CTCTGTGGCT CACTTCAAGA GGAGGCCAGG GTGACGCACA GTGTACTTCA GAGACCCCAG 1680
AGCCACCTGG ACCTGAGTCC CTGTGAATGG ACACGTGACG GGCCTCACTG GGTGTGCAGT 1740
AAGATAAAAC ATCTCCTTAA TCTCAGAGAG AGCCTGTGTT AATAAGCACG TGCCTGGCCT 1800
GGCACCAGAT GCGGCACAGA GAAGAGACGA AGACTAATTA AATCACACAC GTCCAGAGAC 1860
CTCCTTGGTA AGAAAAGCCA CACCGATACA GAGTAGTGTT GTTCTACACA CACACGTGTG 1920
TGTGGGTGTG TGTGTATAGA GAGATATATA TGTATATATT TCATTGGCTC TCTTATGAGC 1980
TACAGTGACT CTAAAAGATG CACCAAGAAA GCAGAGGAAC AAGGGGAAGG GAGGGAAGGG 2040
ACAGAGGCTT TCACACCCCA AATGCTGGGC ATTTTGTGTC TGGATGACCT CAGCCAGTTT 2100
CCACCTACAA AACAGAATAA AAAGAGGCTG GTCCCCAGGG TGTGTAACCT GACACCTCTT 2160
GCCGGCAGCT GAATACAGGG GATTGTTTTT TTAAACTTCA AGTTCCAATC CCTAGTAACA 2220
AAGTGAGGCC TCTCCTGCAA CTAAAGAACC TCCCTGGAAA AATAAATCCT GCTGCCTGTT 2280
TTGTCATCAT CTTCGACAAT TAGCTGTACT TGGGACAACG TGACTCGAGC CAATTGGTGA 2340
AGGCGATTAG GGCATCCACT TAAAAACGCT CTTCACAACT GGTGGAGGGG TGTCCTCTAT 2400
TCCACCCCTG TTCTGCACCC GGTACTTGAG CTGCATTATC TCCTTTCATC TTCACAGCAC 2460
CCCCTGAGAG AGGCTCATTA TCCTCATGTT AGAGATGAGG ACACTGAGAC TCAGAGATGT 2520
TCAGCCCACG CCAAGGTCTA GGACAGAGTG AGGGTGTGGG TTCAGGTCTG GCTGGCTCGG 2580
GCTCCACACT CCCCAGCAGA CCATCTTGCT TCTGTGCTCA GCAGAGCAAG CCTCCCCCAG 2640
CACACACTTC CTACAAACCT CAATGTCAAA GAGCTCCCAG ACCCCATGAC TTCTCCTCTT 2700
CCAAGGGAAG AAGTCAGCAA CACTGCCTCA GACACCCTTA TTCACTCTCA CCCAATCAAA 2760
GAGAATGGTG GAGGTCGCAG GTTCGGCATA AAATACTAAC AAATGACACC ACAGCTGCCT 2820
CTGAGGTCCA TGCTATTGTA TCGAGCATTT AGTATGTCCA GACGCTGTGC TAGGCATTTC 2880
CCACATTACC TTGTTTAAGG CTCACAGCCT TAAGGTGGGT ATTATCAGTC ACATTTCACA 2940
GATGATGCAA CTGAGGAGCA GAAAGTTTTC TCTAGGGTCA CACAGATAGG AAGTAACAGA 3000
GTTTAGACTC AACCCAGGAC TACACCTCAG GGTTCTTCCC CTCCCCCTAG AGCTCTTCCA 3060
TAGCTAAGAC TCTATAACGT GTACTAAGCA GAAAAACCCC TGCCGAGCTC TCCTGACCAT 3120
GTCCTTCTGG TCAATCGGGG TCCTCCCGAG AGCATAGCAA CAGTGCAGCT 3170